SK Hynix plánuje příští měsíc debut na Nasdaqu prostřednictvím ADR a může získat více než 29 miliard USD. Peníze chce použít na nové továrny a vybavení, což může zvýšit nabídku paměťových čipů a vyvinout tlak na ceny.
Massive demand for memory chips for artificial intelligence (AI) training and inference has been a boon for the three major memory chipmakers. Shares of Micron Technology (MU 6.59%) have climbed over 850% in the past year, while its Korean competitors SK Hynix and Samsung Electronics are up nearly 900% and 500%, respectively, in the same period. All three have benefited from a massive supply/demand imbalance, which has allowed them to charge record-high prices for their products.
Now SK Hynix is making a move that should be a warning to Micron investors and the memory market in general. The company will list American depositary receipts on the Nasdaq stock exchange next month. The offer could raise over $29 billion. Here's why Micron investors need to pay attention.
Image source: The Motley Fool.
A massive capital raise for Micron's biggest competitor While we're talking about trillion-dollar companies, make no mistake: $29 billion is still a huge amount of money to raise from the public market. Few other companies have ever raised that much at one time from a stock offering.
That capital has to come from somewhere. With Micron being the only one of the big three memory chipmakers with U.S.-listed shares, it may feel the brunt of the shift in capital as investors look to broaden exposure in the memory market.
The bigger thing Micron investors need to worry about, however, is exactly what SK Hynix plans to do with all that cash. In its SEC filing, management said it intends to use all proceeds to construct new production facilities in Korea and to purchase new fabrication equipment.
Those facilities could start producing new chips before the end of 2027, with a rapid ramp-up in capacity through 2030. It's also constructing an advanced chip packaging facility in Indiana that's set to open in 2028.
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SK Hynix's expansion plans could rapidly increase the total supply of memory chips in a market where products are mostly commoditized. SK Hynix chips can be used in place of Micron chips. As a result, if SK Hynix has more chips to sell, it could gain market share and put pressure on pricing.
Of course, Micron isn't standing still. It's building two factories in Idaho, which are set to open in 2027 and 2028. It also acquired a site in Taiwan where it expects to start production in mid-2027, and it's planning additional projects set to start production later this decade. Overall, management expects supply constraints to persist through the end of next year.
As more supply comes online to meet demand, prices will fall. Overall profits can continue to climb for some time, as more unit sales offset declining market prices. However, profits will eventually fall as supply growth outpaces demand growth, with SK Hynix, Micron, and Samsung all racing to build capacity. SK Hynix's capital raise could accelerate that peak.
Micron investors should exercise caution The current upward earnings cycle in the memory chip market can't last forever. Micron is already taking steps to protect itself against what could be a severe downcycle in a few years. It's signing long-term strategic customer agreements that lock in pricing at a maximum equal to its current price, while also creating a pricing floor.
Many of those agreements run through 2030, and management says they represent about 20% of its dynamic random-access memory (DRAM) chip volume. The agreements could reduce the cyclical downturn later this decade, but it also caps the upside it could generate over the next year or two from increased pricing.
With SK Hynix's aggressive build-out plans about to receive significant capital backing, Micron may be betting on an accelerated timeline toward the market's peak pricing.
The stock price has climbed to about 9 times forward earnings expectations and 8 times fiscal 2028 earnings expectations. If Micron's earnings cycle peaks, as expected, in 2028, it's currently trading for a relatively expensive multiple compared to its historic valuation. If the competition pushes that timeline forward or worsens the downcycle, it could prove way overvalued at today's price.
Nový CEO Occidental Richard Jackson chce v blízké době snížit dluh na 10 miliard USD a zlepšit volný cash flow. Firmu zároveň dál zatěžují vysoké dividendy Berkshire.
SummaryCompaniesCEO Richard Jackson aims to cut debt to $10 billionOccidental to begin repaying $8.5 billion to Berkshire in 2029Investor Bill Smead says Occidental must grow or seek a buyerHOUSTON, June 29 (Reuters) - In not quite a month as Occidental Petroleum's (OXY.N), opens new tab CEO, Richard Jackson has already been challenged with looking for ways to lift a lagging stock price and pay down more debt.
Longer term, Jackson may face a more fundamental question: whether to seek a buyer for the oil company that has a roughly $51 billion market cap.
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Berkshire Hathaway (BRKa.N), opens new tab, whose preferred stake costs Occidental hundreds of millions of dollars in annual dividends, already owns a quarter of the company.
Jackson, who first joined Occidental in 2003, took over the Houston-based company on June 1. He succeeded Vicki Hollub, who ran Occidental for a decade and engineered two major acquisitions that shifted Occidental's oil production heavily toward the U.S.
That positioning has proved advantageous as the U.S.-Israeli war with Iran rattled confidence in Middle East oil supply. Rivals like Exxon Mobil, with roughly 20% of its production in the region, were more exposed to disruptions.
Yet Occidental's acquisitions came at a steep cost and saddled the company with as much as $38.5 billion in long-term debt. Hollub reduced the debt to $15.2 billion by the end of her tenure, during which the share price fell 26%, lagging far behind its peers. Over the same time period, ConocoPhillips returned 153% and Chevron returned 88%.
"The biggest opportunity is to clean up the capital structure, strengthen the balance sheet and increase shareholder returns," said David Byrns, a portfolio manager at American Century Investments, which holds an Occidental stake worth about $131 million, according to LSEG data.
During an earnings call in May, Jackson said his priority was to reduce principal debt to $10 billion in the near term, continue boosting free cash flow and grow oil production organically through technology.
"Richard has been spending time meeting with investors, hearing their points of view and reinforcing that our value improvement starts with executing from a strong balance sheet," an Occidental spokesperson said. GETTING OUT FROM UNDER BERKSHIRE
Occidental acquired Anadarko Petroleum for $55 billion including debt in 2019, aided by a $10 billion investment from Berkshire that requires Occidental to pay the conglomerate an 8% annual dividend. That is a higher payout than the typical junk bond now offers, and spurred criticism that Occidental was rewarding Berkshire much more than its other shareholders.
Occidental has paid off about $1.5 billion of the preferred stock and plans to begin redeeming the rest at a 5% premium when it is eligible to do so in August 2029.
Berkshire also owns 26.9% of Occidental's common stock, with warrants to buy $5 billion more until one year after Occidental redeems the preferred stock.
As a leader, Jackson proved successful at turning around a previously dysfunctional global drilling team, and is well-liked within the company, a former Occidental executive said.
Despite operational improvements so far, Occidental must either make more acquisitions or look for a buyer, said Bill Smead, chief investment officer at Smead Capital Management, which owns a roughly $201 million Occidental position.
The oil industry has seen a wave of mega-mergers in recent years, as producers sought to consolidate and lower operational costs.
"Either Occidental needs to get bigger and beef up the oil in the tank, or they're probably going to have to be part of a larger oil and gas company," Smead said.
Occidental and Berkshire should make clear whether they intend for Occidental to eventually become a subsidiary of the conglomerate, he added. Billionaire Warren Buffett, who was Berkshire's CEO at the time of its investment in Occidental, has said he did not plan to buy the company. Berkshire, whose new CEO is Greg Abel, declined to comment.
Berkshire's large stake limits interest in Occidental from potential acquirers, Smead said. "It keeps other investors from being aggressive."
Reporting by Sheila Dang in Houston; Additional reporting by Jonathan Stempel; Editing by Nathan Crooks and David Gregorio
Our Standards: The Thomson Reuters Trust Principles., opens new tab
Honeywell Technologies oznámila, že ve čtvrtek 23. července zveřejní hospodářské výsledky za 2. čtvrtletí před otevřením burzy Nasdaq a probere výhled na rok 2026. Součástí budou i výsledky bývalé Aerospace Technologies, nyní Honeywell Aerospace (HONA).
, /PRNewswire/ -- Honeywell Technologies (NASDAQ: HON) today announced it will issue its second quarter financial results before the opening of the Nasdaq Stock Market on Thursday, July 23. The results for the second quarter will include the former Aerospace Technologies segment, which is now operating as Honeywell Aerospace and trading on Nasdaq under the ticker symbol "HONA" following the spin-off from Honeywell today. Honeywell Technologies will hold a conference call at 8:30 a.m. EDT to discuss its second quarter performance and 2026 outlook.
Presentation Materials / Webcast Details
A real-time audio webcast of the presentation can be accessed at investor.honeywell.com, where related materials will be posted prior to the presentation and a replay of the webcast will be available for 30 days following the presentation.
Honeywell Technologies is a global, pure-play automation company with a legacy of innovating to help solve the world's most mission-critical challenges, enhancing the quality of life for people and communities around the world. We serve the building, industrial, and process sectors with a broad portfolio of services, solutions, and products, underpinned by our Honeywell Technologies Accelerator operating system and Honeywell Technologies Forge intelligence layer. By combining the deep domain expertise of our more than 50,000 employees with decades of data from our global installed base, we are uniquely positioned to lead the industrial sector's transition from automation to autonomy. For more news and information on Honeywell Technologies, please visit Honeywell Technologies Newsroom.
Honeywell Technologies uses our Investor Relations website, investor.honeywell.com, as a means of disclosing information which may be of interest or material to our investors and for complying with disclosure obligations under Regulation FD. Accordingly, investors should monitor our Investor Relations website, in addition to following our press releases, SEC filings, public conference calls, webcasts, and social media.
June 29, 2026 06:55 ET | Source: Scotts Miracle-Gro Company (The)
Nate Baxter Appointed President and Chief Executive Officer
Pete Shumlin Elected Chairman of the Board
MARYSVILLE, Ohio, June 29, 2026 (GLOBE NEWSWIRE) -- The Scotts Miracle-Gro Company (NYSE: SMG), the leading marketer of branded consumer lawn and garden products in North America, today announced that the Board of Directors has named Nate Baxter as president and CEO, effective immediately. In addition, Baxter has joined the Board of Directors. The Board also elected independent Lead Director Pete Shumlin as chairman of the Board.
Baxter succeeds Jim Hagedorn, 70, CEO since 2001 and chairman since 2003, whose transition from the Company and its Board of Directors aligns with the Board’s long-term internal succession plan. The framework of the succession plan was established by the Board of Directors upon Baxter joining the Company in 2023.
During his tenure, Baxter, 53, has driven a relentless focus on operational excellence and is the architect of the Company’s multi-year SMG 2.0 growth strategy centered on category growth, channel expansion and product innovation grounded in naturals and organics. He also has spearheaded the implementation of technology, automation, data analytics and AI to deliver operational and cost efficiencies throughout the organization.
Hagedorn completed a nearly 40-year career with the Company, having held sales, operations and management roles before becoming CEO and chairman. Hagedorn, whose father Horace started Miracle-Gro in 1951, led the merger of the family business with The Scotts Company in 1995. In his time as CEO, he shaped the modern lawn and garden industry through acquisitions of key brands, such as Ortho and Tomcat, that significantly expanded the portfolio and through strategic growth initiatives that included the joint venture with Bonnie Plants. He advanced new approaches to consumer marketing and led the public listing of SMG on the New York Stock Exchange. Annual revenue climbed from $732 million in 1995 after the Scotts and Miracle-Gro merger to $3.3 billion in fiscal 2025.
“Jim has made ScottsMiracle-Gro what it is today and fundamentally modernized the lawn and garden industry by championing the consumer experience,” Shumlin said. “As a former F-16 fighter pilot, he brought a boldness and competitive spirit to the Company that remains a big part of the associate experience. He has given most of his adult life to this Company, and we are eternally grateful.
“As for Nate’s appointment as chief executive officer, this is the realization of the Board’s internal succession planning efforts with an eye toward accelerating next-generation growth drivers to scale the business. Nate has proven to be an exceptional talent who leads with integrity, collaboration, vision and operational expertise. He is the architect of the SMG 2.0 growth plan and has built a strong team to execute upon it. He is uniquely qualified to further evolve ScottsMiracle-Gro into the essential, lifestyle brand for lawn and garden consumers of today and the future.”
Baxter added, “I consider it a tremendous privilege to lead ScottsMiracle-Gro and serve all those we touch daily. I know I have big shoes to fill and look forward to collaborating with our teams as we nurture a culture in which our associates thrive and work together to deliver on the SMG 2.0 strategy. We have a special consumer franchise with a meaningful runway. My focus is to build on the momentum of SMG 2.0 while maintaining the financial discipline that has strengthened our balance sheet, converting that into durable shareholder value creation.”
Hagedorn said, “It has been an honor to be part of this Company for most of my life. I’m grateful for the opportunity to work with so many talented people as we built ScottsMiracle-Gro and its brands into the market leader with superpowers like no other in lawn and garden. Nate is ready to take over the reins. He has established himself as the leader ScottsMiracle-Gro needs as it transforms for the future.”
Fiscal 2026 Outlook
In connection with today’s announcement, the Company has reaffirmed its previously provided Fiscal 2026 guidance, which includes:
U.S. Consumer net sales low single-digit growthNon-GAAP adjusted gross margin of at least 32%Non-GAAP adjusted net income per share from continuing operations of $4.15 to $4.35Non-GAAP adjusted EBITDA mid single-digit growthFree cash flow of approximately $275 million, driving leverage ratio down to the high 3s
As previously announced, the Company will host its 2026 Investor Day at the New York Stock Exchange on August 4, 2026, beginning at 9 a.m. ET. Members of the executive and senior leadership team will discuss the Company’s mid- to long-term strategic priorities and financial goals followed by a question-and-answer session.
Bios
Baxter joined the Company in April 2023 as executive vice president, technology and operations, and was named COO in September 2023 before taking on the expanded role of president and COO in 2024. Among his responsibilities were execution of Company strategies and oversight of the market-leading brands, sales, supply chain, marketing, R&D and information technology. Prior to ScottsMiracle-Gro, Baxter was president of TEL U.S., a Tokyo Electron Ltd. subsidiary that manufactures semiconductor and flat-panel manufacturing equipment, and worked with Intel Corporation in technology, supply chain, strategy and management. He is a general partner of the Hagedorn Partnership, L.P., the largest shareholder of the Company, and serves as chairman of the board of Bonnie Plants, the largest national supplier of vegetable and herb plants in the U.S., as well as a board member with The Legacy Project, which empowers students to become leaders and innovators.
Shumlin, 70, a former three-term governor of Vermont and director at Putney Student Travel as well as a principal in numerous real estate ventures, has been a member of the Board of Directors since 2017 and served as its lead independent director since 2023.
About ScottsMiracle-Gro
With approximately $3.3 billion in sales, the Company is the leading marketer of branded consumer lawn and garden products in North America. The Company’s brands are among the most recognized in the industry. The Company’s Scotts®, Miracle-Gro®, Ortho® and Tomcat® brands are market-leading in their categories. For additional information, visit us at www.scottsmiraclegro.com.
For investor inquiries:
Brad Chelton
Vice President
Treasury, Tax and Investor Relations [email protected]
(937) 309-2503
For media inquiries:
Tom Matthews
Chief Communications Officer [email protected]
(937) 844-3864
Viatris oznámil pozitivní výsledky fáze 3 pro VR-205 u japonských dospělých s primární IgAN; lék splnil hlavní i klíčové sekundární cíle a byl dobře snášen. Podání žádosti o registraci v Japonsku směřuje do konce roku 2026.
VR-205 Met Primary Endpoint and Key Secondary Endpoints and Was Well Tolerated
VR-205 Efficacy and Safety Profile in Japanese Patients Was Consistent with the Profile Observed in Global Studies
Japanese New Drug Application Submission Targeted by End of 2026
, /PRNewswire/ -- Viatris Inc. (Nasdaq: VTRS), a global healthcare company, today announced positive top-line results from a Phase 3 clinical trial evaluating the efficacy and safety of VR-205 (targeted-release budesonide formulation) (Nefecon®) in Japanese adult patients with primary immunoglobulin A nephropathy (IgAN) at risk of developing end-stage renal disease.
The Phase 3 clinical trial was a multicenter, interventional, open-label study designed to evaluate the efficacy and safety of 16 mg of VR-205 in Japanese adult patients with primary IgAN. Patients were treated for nine months, followed by a three-month follow-up period.
The study achieved its primary endpoint, with VR-205 demonstrating a 33.75 percent reduction in geometric mean urine protein-to-creatinine ratio (UPCR) at 9 months compared to baseline [95% CI: -45.27 to -19.80; p < 0.001]. These results were statistically significant and clinically meaningful, and were consistent with those observed in the global Phase 3 program for the product. Key findings included:
In addition to a statistically significant and clinically meaningful reduction in UPCR at 6 and 12 months, VR-205 demonstrated a significant improvement in estimated glomerular filtration rate (eGFR) and reductions in serum creatinine and urine albumin-to-creatinine ratio (UACR) at 9 months compared to baseline. The overall therapeutic benefit of VR-205 was further supported by improvements in microhematuria and a sustained proteinuria reduction. No study participants progressed to dialysis, kidney transplant or severe renal impairment (eGFR ≤15 mL/min per 1.73 m2) by the end of the study. VR-205 was generally well tolerated over the nine-month treatment period, with a safety profile consistent with the known safety profile of targeted-release budesonide in non-Japanese patients. "We are pleased with these top-line results, which highlight VR-205 as a potentially meaningful, disease-modifying treatment option for patients with primary IgAN," said Viatris Chief R&D Officer Philippe Martin. "In Japan, where IgAN incidence is the highest globally, VR-205 could become the first IgAN-specific, targeted-release budesonide oral therapy. This progress reflects the continued execution of Viatris' strategy focused on building a differentiated and increasingly innovative portfolio in Japan, with an emphasis on delivering therapies that provide meaningful value and address significant unmet needs."
"Primary IgAN is a designated intractable disease in Japan, and remains a significant unmet need, with no curative treatment despite the risk of progression to end-stage renal disease," said Yuko Asami, Head of R&D, Viatris Japan. "These top-line results mark an important step toward expanding treatment options for patients and healthcare providers."
Viatris is targeting submission of a New Drug Application in Japan by the end of 2026.
In 2022, Calliditas Therapeutics AB and Viatris Pharmaceuticals Japan Inc., a subsidiary of Viatris Inc., entered into an exclusive license agreement to obtain marketing authorization and to commercialize VR-205 for the treatment of primary IgAN in Japan. It is currently a specialty drug approved and marketed as Tarpeyo® in the U.S. and as Kinpeygo® in Europe.
About Phase 3 Study (VR-205A-01-CAZ-3001)
The Phase 3 trial was a multicenter, interventional, open-label study conducted in Japan to evaluate the efficacy and safety of oral VR-205 (targeted-release budesonide formulation) for the treatment of primary IgA nephropathy in Japanese adult patients at risk of developing end-stage renal disease. The study enrolled a total of 39 participants who were treated with 16 mg of VR-205 daily (four capsules) over a nine-month treatment period.
Following completion of treatment, participants entered a three-month follow-up period including a two-week dose tapered to 8 mg of VR-205 (two capsules) daily at the start of the follow-up period.
About Immunoglobulin A Nephropathy (IgAN)
IgAN is a progressive, immune-mediated kidney disease and the most common primary glomerulonephritis worldwide. Japan reports the highest incidence rates globally, at 39 to 45 cases per million population per year, with peak age at diagnosis between 30 and 39 years. In Japan, adult-onset IgAN is reported to progress to end-stage renal disease (dialysis or transplantation) in approximately 15-20 percent of patients within 10 years. Most patients reaching end-stage renal disease face decades of dialysis. The total national cost of maintenance hemodialysis in Japan is approximately JPY 1.5 trillion per year. Chronic glomerulonephritis (with IgAN as a leading underlying cause) accounts for 23.4 percent of Japan's more than 340,000 dialysis patients. Despite this burden, therapies that target the underlying immunological drivers of IgAN to preserve long-term kidney function have remained limited, and a clear need persists for disease-modifying treatment options.
About Viatris
Viatris Inc. (Nasdaq: VTRS) is a global healthcare company whose mission is to empower people worldwide to live healthier at every stage of life. We meet the needs of patients around the world by acting decisively with ingenuity and resolve. Whether we're developing new medicines, working to maintain a resilient supply of needed therapies, or pursuing bold innovation, we strive to deliver solutions that are effective at scale and built to endure. We're purpose-built to make an impact with a dynamic portfolio that spans generics, established brands and innovative medicines that address areas of significant unmet need. We are headquartered in the U.S., with global centers in Pittsburgh, Shanghai, China, and Hyderabad, India. Learn more at viatris.com and investor.viatris.com, and connect with us on LinkedIn, Instagram, YouTube and X.
Forward-Looking Statements
This press release includes statements that constitute "forward-looking statements." These statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements may include statements that positive top-line results from a Phase 3 clinical trial evaluating the efficacy and safety of VR-205 (targeted-release budesonide formulation) (Nefecon®) in Japanese adult patients with primary immunoglobulin A nephropathy (IgAN) at risk of developing end-stage renal disease; VR-205 met primary endpoint and key secondary endpoints, and was well tolerated; VR-205 efficacy and safety profile in Japanese patients was statistically significant and clinically meaningful and were consistent with the profile observed in global studies; we are pleased with these top-line results, which highlight VR-205 as a potentially meaningful, disease-modifying treatment option for patients with primary IgAN; in Japan, where IgAN incidence is the highest globally, VR-205 could become the first IgAN-specific, targeted-release budesonide oral therapy; this progress reflects the continued execution of Viatris' strategy focused on building a differentiated and increasingly innovative portfolio in Japan, with an emphasis on delivering therapies that provide meaningful value and address significant unmet needs; these top-line results mark an important step toward expanding treatment options for patients and healthcare providers; Viatris is targeting submission of a New Drug Application in Japan by the end of 2026. Because forward-looking statements inherently involve risks and uncertainties, actual future results may differ materially from those expressed or implied by such forward-looking statements. Factors that could cause or contribute to such differences include, but are not limited to: the uncertainties inherent in research and development, including the outcomes of clinical trials; the ability to meet anticipated clinical endpoints; the possibility of unfavorable new clinical data and further analyses of existing clinical data; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from clinical studies; failure to achieve the intended benefits of our strategic initiatives and priorities; goodwill or impairment charges or other losses; any changes in or difficulties with the Company's manufacturing facilities; failure to achieve expected or targeted future financial and operating performance and results; Viatris' or its partners' ability to develop, manufacture, and commercialize products; any regulatory, legal or other impediments to Viatris' ability to bring new products to market; products in development and/or that receive regulatory approval may not achieve expected levels of market acceptance, efficacy or safety; actions and decisions of healthcare and pharmaceutical regulators; changes in healthcare and pharmaceutical laws and regulations in the U.S. and abroad; the scope, timing and outcome of any ongoing legal proceedings, and the impact of any such proceedings on Viatris; any significant breach of data security or data privacy or disruptions to our IT systems; risks associated with international operations; changes in third-party relationships; the effect of any changes in Viatris' or its partners' customer and supplier relationships and customer purchasing patterns; the impacts of competition; changes in the economic and financial conditions of Viatris or its partners; uncertainties regarding future demand, pricing and reimbursement for the Company's products; uncertainties and matters beyond the control of management, including but not limited to general political and economic conditions, potential adverse impacts from future tariffs and trade restrictions, inflation rates and global exchange rates; and the other risks described in Viatris' filings with the Securities and Exchange Commission ("SEC"). Viatris routinely uses its website as a means of disclosing material information to the public in a broad, non-exclusionary manner for purposes of the SEC's Regulation Fair Disclosure (Reg FD). Viatris undertakes no obligation to update these statements for revisions or changes after the date of this press release other than as required by law.
Biogen na AAIC 2026 ukáže nová data z fáze 2 studie CELIA pro diranersen u časné Alzheimerovy choroby, včetně klinických, biomarkerových a bezpečnostních výsledků. Představí také nové analýzy lecanemabu.
Diranersen presentation will feature Phase 2 CELIA data in early Alzheimer’s disease, including clinical, biomarker and safety results for Biogen’s investigational tau-targeting ASO, following topline results announced in May 2026Lecanemab presentations will highlight emerging data on subcutaneous administration and real-world use, including practical treatment considerations, at-home administration, three-year LEADER data, maintenance dosing and patient experienceAdvances across Biogen’s Alzheimer’s disease portfolio underscore its leadership and continued commitment to innovation in Alzheimer’s care, spanning treatment delivery, real-world evidence and approaches targeting core pathologies, including amyloid and tau
CAMBRIDGE, Mass., June 29, 2026 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) today announced it will present new data across its Alzheimer’s disease portfolio at the Alzheimer’s Association International Conference (AAIC) 2026, taking place July 12-15 in London, UK. Presentations will include data from the Phase 2 CELIA study evaluating diranersen, an investigational tau-targeting antisense oligonucleotide (ASO), and new analyses from studies of LEQEMBI® (lecanemab).
“Biogen remains committed to advancing innovation across Alzheimer’s care, from treatment delivery and real-world evidence generation to continued progress in addressing core pathologies, including amyloid and tau. Tau has long remained one of the most important targets in Alzheimer’s disease, and the Phase 2 CELIA topline results for diranersen reinforce the potential of tau reduction as a therapeutic approach in early Alzheimer’s disease,” said Priya Singhal, M.D., M.P.H., Executive Vice President and Head of Development at Biogen. “We look forward to presenting initial data from this pioneering study as well as new data on lecanemab on the global stage at AAIC.”
Featured Scientific Sessions and Presentations
Diranersen
Diranersen is an investigational ASO that targets MAPT RNA to reduce tau production at its source, a differentiated approach to addressing abnormal tau both inside and outside neurons. At AAIC, Biogen will present clinical, biomarker and safety data that build on the May 2026 topline announcement and further characterize diranersen as the program advances toward Phase 3 development.
Topline Results from CELIA: A Phase 2 Study to Evaluate the Tau-Targeting ASO Diranersen (BIIB080) in Patients with Early Alzheimer’s Disease
Developing Topics Session: Developing Topics in Phase 2 Clinical Trials,
Tuesday, July 14, 2:00–3:30 PM BST This presentation will feature data from CELIA, an 18-month Phase 2 study evaluating diranersen, Biogen’s investigational tau-targeting ASO, in patients with early Alzheimer’s disease. The presentation will include initial clinical, biomarker and safety results from the study.
Lecanemab
Featured lecanemab sessions at AAIC will highlight continued progress in the treatment landscape for early Alzheimer’s disease, with data spanning subcutaneous administration, including at-home use, practical treatment considerations, and three-year real-world evidence from the multicenter LEADER study.
Developing Topics Session: Lecanemab Subcutaneous Formulation in Early Alzheimer's Disease: Emerging Clinical Evidence and Practical Use Considerations
Sunday, July 12, 4:15–5:45 PM BST This session will feature presentations on the emerging clinical evidence, safety profile, practical use considerations and real-world patient experience with subcutaneous lecanemab administration in early Alzheimer’s disease.
Featured Research Session: Lecanemab Three Years Post-Approval: A Comprehensive Multicenter, Real-World, Retrospective Study (LEADER) in Diverse U.S. Clinical Settings
Tuesday, July 14, 4:15–5:45 PM BST This session will feature new real-world evidence from the LEADER study, including findings on lecanemab use and outcomes across diverse U.S. clinical settings, once-monthly maintenance dosing, patient pathways and physician and perceived patient satisfaction with maintenance therapy.
Selected Additional Oral and Poster Presentations
The following selected presentations highlight additional areas of Alzheimer’s disease research being presented at AAIC, including lecanemab-related data. For a complete list of presentations, please refer to the AAIC scientific program.
Real-world Insights into Clinician Involvement and Testing Approaches for Mild Cognitive Impairment and Alzheimer’s
Monday, July 13, 7:30 AM–4:15 PM BST Continued or Time-limited Treatment Benefits of Anti-amyloid Monoclonal Antibodies in Early Alzheimer’s Disease
Monday, July 13, 7:30 AM–4:15 PM BST
Lecanemab Treatment for Alzheimer’s Disease in Real-World Clinical Practice: A Multicenter, Surveillance Safety Study from the Alzheimer’s Network for Treatment and Diagnostics (ALZ-NET) Registry
Tuesday, July 14, 9:00–10:30 AM BST
Impact of Biomarker Modalities in the Diagnostic Evaluation of Patients with Suspected Alzheimer’s Disease: A US Retrospective Study
Wednesday, July 15, 7:30 AM–4:15 PM BST Estimating the Economic Impact of Delayed Alzheimer’s Disease Progression with Lecanemab
Wednesday, July 15, 7:30 AM–4:15 PM BST Educational Program on Tau in Alzheimer’s Disease
At AAIC, Biogen will host an interactive booth offering an immersive journey into the role of tau in Alzheimer’s disease, from pathology to clinical presentation. Biogen is also expanding its educational efforts with a new e-learning module on KnowTau.com, building on the resources already available.
For more information, please see the AAIC 2026 program and visit the Biogen AAIC booth.
About diranersen (BIIB080)
Diranersen (BIIB080) is an investigational antisense oligonucleotide (ASO) therapy designed to target microtubule-associated protein tau (MAPT) mRNA to reduce the production of tau protein. Unlike many investigational approaches that have focused on targeting extracellular tau, diranersen is designed to reduce both intracellular and extracellular tau.
Diranersen is being investigated as a potential treatment for early Alzheimer’s disease. In 2025, the U.S. Food and Drug Administration (FDA) granted Fast Track designation to diranersen for the treatment of Alzheimer’s disease.
In December 2019, Biogen exercised a license option with Ionis Pharmaceuticals and obtained a worldwide, exclusive, royalty-bearing license to develop and commercialize diranersen. Diranersen was discovered by Ionis.
About the CELIA Study
CELIA is a global Phase 2 randomized, double-blind, placebo-controlled, dose-ranging study evaluating the efficacy, safety and tolerability of diranersen in individuals with early Alzheimer’s disease. The study enrolled 416 participants with mild cognitive impairment due to Alzheimer’s disease or mild Alzheimer’s disease dementia. All participants enrolled in CELIA had not previously received anti-amyloid therapy.
The study evaluated three doses of diranersen administered intrathecally over an 18-month placebo-controlled treatment period: 60 mg every six months, 115 mg every six months, and 115 mg every three months.
The primary endpoint of CELIA was assessment of dose response for change from baseline on the Clinical Dementia Rating–Sum of Boxes (CDR-SB) at Week 76. Secondary and exploratory endpoints included additional clinical, biomarker and imaging measures, including cerebrospinal fluid tau biomarkers and tau positron emission tomography (PET). Additional information on the CELIA study design is available in the ClinicalTrials.gov listing for the CELIA study.
An ongoing long-term extension (LTE) study is continuing to evaluate the long-term safety, tolerability and durability of diranersen in early Alzheimer’s disease.
About LEQEMBI ® (lecanemab)
LEQEMBI (lecanemab) is the result of a strategic research alliance between Eisai and BioArctic. LEQEMBI is a humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody directed against aggregated soluble protofibril and insoluble forms of amyloid beta (Aβ). LEQEMBI is indicated in the U.S. for the treatment of Alzheimer’s disease and treatment should be initiated in patients with mild cognitive impairment or mild dementia stage of disease, the population in which treatment was initiated in clinical trials. The U.S. Food and Drug Administration (FDA) granted LEQEMBI traditional approval on July 6, 2023. Lecanemab has been approved in 53 countries and regions, including Japan, the United States, China, Europe, South Korea, Taiwan and Saudi Arabia, and is under regulatory review in 6 countries. Following the initial treatment phase with intravenous dosing every two weeks for 18 months, intravenous maintenance dosing every four weeks has been approved in 7 countries, including the U.S., China and the UK, with applications filed in additional countries and regions. In the U.S., FDA approved LEQEMBI IQLIK™ for once-weekly subcutaneous maintenance dosing in August 2025. A supplemental Biologics License Application for LEQEMBI IQLIK as a once-weekly subcutaneous starting dose is currently under FDA Priority Review, with a Prescription Drug User Fee Act action date of August 24, 2026.
Eisai and Biogen have been collaborating on the joint development and commercialization of Alzheimer’s disease treatments since 2014. Eisai serves as the lead of LEQEMBI development and regulatory submissions globally, with both companies co-commercializing and co-promoting the product and Eisai having final decision-making authority.
Please see full U.S. Prescribing Information for LEQEMBI, including Boxed WARNING and Medication Guide.
About Biogen
Founded in 1978, Biogen is a leading biotechnology company that pioneers innovative science to deliver new medicines to transform patients’ lives and to create value for shareholders and our communities. We apply deep understanding of human biology and leverage different modalities to advance first-in-class treatments or therapies that deliver superior outcomes. Our approach is to take bold risks, balanced with return on investment to deliver long-term growth.
We routinely post information that may be important to investors on our website at www.biogen.com. Follow us on social media - Facebook, LinkedIn, X, YouTube.
Biogen Safe Harbor
This news release contains forward-looking statements, including, among others, relating to: the potential benefits, efficacy and safety of diranersen (BIIB080) and lecanemab (LEQEMBI); the potential to advance care and improve outcomes for, and address unmet needs of, patients with Alzheimer’s disease; potential regulatory discussions, submissions, decisions and approvals and the timing thereof; the anticipated benefits, risks and potential of our collaboration arrangements; the potential of our commercial business and pipeline programs, including Biogen’s Alzheimer’s disease portfolio; and risks and uncertainties associated with drug development and commercialization. These forward-looking statements may be accompanied by such words as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “forecast,” “goal,” “guidance,” “hope,” “intend,” “may,” “objective,” “outlook,” “plan,” “possible,” “potential,” “predict,” “project,” “prospect,” “should,” “target,” “will,” “would” or the negative of these words or other words and terms of similar meaning. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical trials may not be indicative of full results or results from later stage or larger scale clinical trials and do not ensure regulatory approval. You should not place undue reliance on these statements. Given their forward-looking nature, these statements involve substantial risks and uncertainties that may be based on inaccurate assumptions and could cause actual results to differ materially from those reflected in such statements.
These forward-looking statements are based on management’s current beliefs and assumptions and on information currently available to management. Given their nature, we cannot assure that any outcome expressed in these forward-looking statements will be realized in whole or in part. We caution that these statements are subject to risks and uncertainties, many of which are outside of our control and could cause future events or results to differ materially from those stated or implied in this document, including, among others, uncertainty of our long-term success in developing, licensing, or acquiring other product candidates or additional indications for existing products; expectations, plans, prospects and timing of actions relating to product approvals, approvals of additional indications for our existing products, sales, pricing, growth, reimbursement and launch of our marketed and pipeline products; the potential impact of increased product competition in the biopharmaceutical and healthcare industry, as well as any other markets in which we compete, including increased competition from new originator therapies, generics, prodrugs and biosimilars of existing products and products approved under abbreviated regulatory pathways; our ability to effectively implement our corporate strategy; difficulties in obtaining and maintaining adequate coverage, pricing, and reimbursement for our products; the drivers for growing our business, including our dependence on collaborators and other third parties for the development, regulatory approval, and commercialization of products and other aspects of our business, which are outside of our full control; risks related to commercialization of biosimilars, which is subject to such risks related to our reliance on third-parties, intellectual property, competitive and market challenges and regulatory compliance; the risk that positive results in a clinical trial may not be replicated in subsequent or confirmatory trials or success in early stage clinical trials may not be predictive of results in later stage or large scale clinical trials or trials in other potential indications; risks associated with clinical trials, including our ability to adequately manage clinical activities, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, regulatory authorities may require additional information or further studies, or may fail to approve or may delay approval of our drug candidates; and the occurrence of adverse safety events, restrictions on use with our products, or product liability claims; and any other risks and uncertainties that are described in reports we have filed with the U.S. Securities and Exchange Commission, which are available on the SEC’s website at www.sec.gov.
These statements speak only as of the date of this press release and are based on information and estimates available to us at this time. Should known or unknown risks or uncertainties materialize or should underlying assumptions prove inaccurate, actual results could vary materially from past results and those anticipated, estimated or projected. Investors are cautioned not to put undue reliance on forward-looking statements. A further list and description of risks, uncertainties and other matters can be found in our Annual Report on Form 10-K for the fiscal year ended December 31, 2025 and in our subsequent reports on Form 10-Q. Except as required by law, we do not undertake any obligation to publicly update any forward-looking statements whether as a result of any new information, future events, changed circumstances or otherwise.
Digital Media Disclosure
From time to time we have used, or expect in the future to use, our investor relations website (investors.biogen.com), the Biogen LinkedIn account (linkedin.com/company/biogen-) and the Biogen X account (https://x.com/biogen) as a means of disclosing information to the public in a broad, non-exclusionary manner, including for purposes of the SEC’s Regulation Fair Disclosure (Reg FD). Accordingly, investors should monitor our investor relations website and this social media channel in addition to our press releases, SEC filings, public conference calls and webcasts, as the information posted on them could be material to investors.
EXIM schválil financování FuelCell Energy ve výši 49 milionů USD na podporu vývozu americké čisté energetiky. První tranše má podpořit dodávku pěti bloků o výkonu 2,8 MW do Gyeonggi Green Energy v Jižní Koreji.
June 29, 2026 07:30 ET | Source: FuelCell Energy, Inc.
DANBURY, Conn., June 29, 2026 (GLOBE NEWSWIRE) -- FuelCell Energy, Inc. (Nasdaq: FCEL) announced that the Board of Directors of the Export-Import Bank of the United States (EXIM) approved a financing package on June 23, 2026, of $49 million to be disbursed in two tranches.
The first tranche, expected to disburse on June 30, 2026, provides the company with net proceeds of approximately $22 million after financing fees and customary expenses and reserves to support the delivery of five 2.8-megawatt (MW) FuelCell Energy Blocks to Gyeonggi Green Energy (GGE) in South Korea. With nearly 60 MW of installed capacity, GGE’s site is among the largest fuel cell installations in the world and serves as an important example of distributed utility-scale clean energy deployment. A second tranche is expected to be disbursed in October 2026, subject to customary closing conditions.
EXIM structured the financing under its loan guarantee program and arranged with Private Export Funding Corporation (PEFCO), supporting the export of American clean energy technology to international markets. It builds upon FuelCell Energy’s prior EXIM-supported financing completed in 2024 and 2025 and reflects continued support for the company’s export of U.S.-manufactured clean energy technology.
“EXIM’s approval validates the strength of this project, our partnership with Gyeonggi Green Energy, FuelCell Energy’s business plan, and our ability to deliver distributed utility-scale clean power globally,” said Michael Bishop, FuelCell Energy’s Chief Financial Officer. “This financing adds non-dilutive capital to support growth and provides added flexibility as we invest in scaling manufacturing capacity, pursuing strategic opportunities in global power markets and mirroring our distributed utility scale solutions to AI factories and data centers.”
FuelCell Energy manufactures its clean, baseload fuel cell technology in Torrington, Conn., supporting domestic manufacturing, U.S. supply chains, and skilled American jobs. The transaction aligns with EXIM’s mission to support U.S. manufacturing, exports, and global competitiveness. Approximately 90% of the content in FuelCell Energy Blocks is sourced from the United States.
About FuelCell Energy
FuelCell Energy, Inc. is an American clean energy technology company delivering continuous, scalable baseload power for mission critical applications globally. The company’s fuel cell systems generate electricity directly at the point of use, enabling reliable, low emissions power for data centers, industrial facilities, utilities, and distributed generation customers. FuelCell Energy delivers commercially proven, modular, utility-scale systems—backed by global fuel cell deployments approaching one gigawatt. Learn more at www.fuelcellenergy.com.
Global Net Lease od začátku druhého čtvrtletí prodala aktiva za 74 milionů USD, z toho 66 milionů USD obsazených nemovitostí, včetně 61 milionů USD kancelářských aktiv s hotovostní cap rate 7,2 %. Tím dál snižuje expozici vůči kancelářím.
June 29, 2026 06:00 ET | Source: Global Net Lease, Inc.
Sold $66 Million of Occupied Properties, Including $61 Million of Office Assets at a 7.2% Cash Cap Rate Office Assets Accounted for 93% of Occupied Sales Disposition Activity Reduces Office Exposure and Supports Continued Focus on Leverage ReductionPending Acquisition of Modiv Industrial Remains on Track for Anticipated Third Quarter 2026 Closing NEW YORK, June 29, 2026 (GLOBE NEWSWIRE) -- Global Net Lease, Inc. (NYSE: GNL) ("GNL" or the "Company") today announced that, since the first quarter 20261, it sold $74 million of assets, including $66 million of occupied assets at a 7.2% cash cap rate, with office assets representing $61 million, or 93%, of occupied dispositions. GNL also sold $8 million of vacant assets, eliminating negative NOI drag, increasing portfolio occupancy and enhancing overall portfolio quality. Year-to-date, GNL has now closed approximately $145 million of dispositions at a 7.5% cash cap rate on occupied assets.
Since the first quarter 20261, GNL sold two occupied office assets at a 7.2% cash cap rate: a 33,000-square-foot building leased to the U.S. General Services Administration ("GSA") for $13 million and a 369,000-square-foot office building leased to GE Aviation for $48 million. Prior to the sales, GNL executed 20-year and 10-year lease extensions at the GSA and GE Aviation properties, respectively, increasing the assets' marketability and positioning them for dispositions at enhanced values. In addition, GNL has a 133,000-square-foot office asset in the Netherlands, currently leased to Koninklijke KPN N.V. ("KPN"), under contract for sale for approximately $18 million2, upon the expiration of KPN's lease in December 2026. These transactions reflect the Company's continued execution of its strategy to reduce office exposure, proactively address lease rollover risk, and improve the long-term quality of the portfolio. GNL is continuing its efforts to further reduce its office exposure and looks forward to providing additional details for any potential transaction entered into. Upon completion of these transactions, GNL expects office exposure to be reduced to approximately 21% of portfolio straight-line rent.
On the acquisition front, GNL is currently under contract to acquire a 100,000-square-foot single-tenant industrial property occupied by a Fortune 50 investment-grade tenant for $14 million at an 8.2% cash cap rate. The Company anticipates that this acquisition will provide an opportunity to redeploy disposition proceeds into a high-quality industrial asset at an attractive yield.
Together with the pending $535 million acquisition of Modiv Industrial, Inc. (NYSE: MDV), expected to close in the third quarter of 2026, these initiatives reflect GNL's continued focus on increasing exposure to single-tenant industrial and retail assets while strategically reducing office concentration. The acquisition is expected to be immediately 4% accretive to AFFO per share and is structured to be leverage neutral, complementing GNL's broader, continued focus on reducing leverage over the long-term and preserving GNL's balance sheet strength and financial flexibility. Through the transaction, GNL will be acquiring a high-quality industrial net lease portfolio with a 15.0 year weighted average lease term and 2.4% average annual rent escalations, which is expected to extend GNL's weighted average lease term from 5.9 years in Q1'26 to 6.7 years on a pro-forma basis.
"Our recent disposition activity advances our strategy of reducing office exposure while improving overall portfolio quality," said Michael Weil, CEO of GNL. "These dispositions demonstrate our ability to monetize office assets at attractive valuations while redeploying capital into high-quality industrial and retail investments. Together with the pending Modiv acquisition and additional office sales, we expect to reduce our office exposure to approximately 21% of portfolio straight-line rent, down from approximately 26% as of the first quarter of 2026, marking another meaningful step in our ongoing portfolio transformation. We believe these actions will further improve portfolio quality, strengthen our earnings profile, and position GNL to deliver long-term value for our stockholders."
About Global Net Lease, Inc.
Global Net Lease, Inc. (NYSE: GNL) is a publicly traded real estate investment trust that focuses on acquiring and managing a global portfolio of income-producing net lease assets across the U.S., and Western and Northern Europe. Additional information about GNL can be found on its website at www.globalnetlease.com.
Footnotes
[1] Represents dispositions closed from April 1, 2026 through June 26, 2026.
[2] Based on an EUR exchange rate as of June 26, 2026.
Important Notice
The statements in this press release that are not historical facts may be forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements involve risks and uncertainties that could cause the outcome to be materially different. The words such as "may," "will," "seeks," "anticipates," "believes," "expects," "estimates," "projects," "potential," "predicts," "plans," "intends," "would," "could," "should" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These forward-looking statements are subject to a number of risks, uncertainties and other factors, many of which are outside of GNL's control, which could cause actual results to differ materially from the results contemplated by the forward-looking statements. These risks and uncertainties include the risks that any potential future acquisition or disposition by GNL, including the Modiv transaction and the pending KPN disposition and industrial property acquisition, is subject to market conditions, capital availability and timing considerations and may not be identified or completed on favorable terms, or at all. Some of the risks and uncertainties, although not all risks and uncertainties, that could cause GNL's actual results to differ materially from those presented in GNL's forward-looking statements are set forth in the "Risk Factors" and "Quantitative and Qualitative Disclosures about Market Risk" sections in GNL's Annual Report on Form 10-K, its Quarterly Reports on Form 10-Q, and all of its other filings with the U.S. Securities and Exchange Commission, as such risks, uncertainties and other important factors may be updated from time to time in GNL's subsequent reports. Further, forward-looking statements speak only as of the date they are made, and GNL undertakes no obligation to update or revise any forward-looking statement to reflect changed assumptions, the occurrence of unanticipated events or changes to future operating results over time, unless required by law.
Comcast plánuje oddělit mediální a technologické aktivity do dvou veřejně obchodovaných firem, včetně daňově neutrálního spin-offu NBCUniversal a Sky. Akcie v předobchodní fázi vyskočily až o 26 %.
Comcast said Monday it plans to separate its media and technology businesses into two publicly traded companies as it looks to better compete in a media landscape increasingly characterized by pressure from streaming rivals and consolidation.
The separation, which will happen via a tax-free spin-off of NBCUniversal and Sky, is expected to be completed in about one year, and Comcast shareholders will own shares in both Comcast and NBCUniversal, the company said in a statement.
Comcast shares jumped as much as 26% in premarket trading.
Comcast co-CEO Mike Cavanagh will become CEO of NBCUniversal, while Comcast's former Chief Financial Officer Michael Angelakis will become CEO of Comcast.
Comcast's other co-CEO and chair, Brian L. Roberts, will continue to be actively involved in the leadership of both Comcast and NBCUniversal.
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"The transaction we are announcing will unlock a more entrepreneurial management approach and open up a multitude of new opportunities for each business," Roberts said.
"Comcast will continue to build on its leadership in connectivity, while NBCUniversal, together with Sky, will have the scale, brands, content and financial resources to compete as a premier global media and entertainment company," Cavanagh said.
Comcast said it expects to retain a stake of up to 19.9% ownership position in NBCUniversal for up to one year after the transaction is completed, which it intends to tax-efficiently monetize over time.
It comes as Comcast's share price has plummeted 30% over the past 12 months amid significant challenges facing the media industry that are driven by the shift away from the TV bundle and toward streaming.
Comcast shares over the past year.
Earlier this year, it completed the spin-off of its portfolio of cable TV networks and digital assets, which includes CNBC and MS Now, to the separate public company Versant Media.
The media sector has seen a wave of consolidation recently, as legacy players strive for scale, with few companies going public amid the challenging environment.
Paramount Skydance completed its merger last year, and earlier this month, it won DOJ approval for a $110 billion deal for Warner Bros. Discovery. Meanwhile, Fox entered an agreement to acquire Roku for $22 billion earlier this month.
— CNBC's Lillian Rizzo contributed to this report
Disclosure: Versant is the parent company of CNBC.
Natera a Aveta Biomics uzavřely partnerství pro globální fázi 3 registrační studii AVTA 30-01 s APG-157 u lokálně pokročilého spinocelulárního karcinomu hlavy a krku. Do studie se zapojí Signatera pro sledování molekulární odpovědi a minimální reziduální nemoci (MRD).
Signatera™ will be used to evaluate molecular response to APG-157 in the neoadjuvant, induction, and adjuvant settings
AUSTIN, Texas & BEDFORD, Mass.--(BUSINESS WIRE)--Natera, Inc. (NASDAQ: NTRA), a global leader in cell-free DNA and precision medicine, and Aveta Biomics, Inc., a clinical-stage immuno-oncology company advancing first-in-class oral immunotherapies for solid tumors, today announced a strategic partnership supporting AVTA 30-01, Aveta’s global Phase 3 registrational clinical trial evaluating APG-157 in patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) (NCT07667296).
APG-157 is Aveta's first-in-class oral immunotherapy intended to expand the benefits of immunotherapy to both immune-cold and immune-hot tumors in patients with LA-HNSCC. APG-157 has received FDA Fast Track and Orphan Drug Designations for this indication.
AVTA 30-01 builds upon previously reported Phase 2 clinical data of APG-157 monotherapy in demonstrating favorable safety, evidence of tumor-control, deep molecular responses, and encouraging event-free survival outcomes. The trial will incorporate serial Signatera testing to assess molecular residual disease (MRD) and treatment response throughout therapy and follow-up. Circulating tumor DNA (ctDNA) has emerged as one of the most promising approaches for detecting MRD and identifying recurrence earlier than conventional imaging alone.
Approximately 826 patients are expected to be enrolled across North America, Europe, Asia-Pacific, and Australia. The study includes separate randomized cohorts for resectable and unresectable locally advanced disease, each with treatment and control arms, and Signatera will be a secondary endpoint. The trial is expected to begin enrollment in 2H’26.
Global annual incidence of head and neck cancer is approximately 950,000,1 and disease recurrence remains a major cause of mortality despite advances in surgery, radiation therapy, and immunotherapy.
“Patients with locally advanced head and neck cancer continue to face substantial risks of recurrence despite aggressive treatment,” said Parag Mehta, Ph.D., founder and chief executive officer of Aveta Biomics. “We believe APG-157 has the potential to transform treatment by activating anti-tumor immunity in both immune-cold and immune-hot tumors. Incorporating serial Signatera testing into AVTA 30-01 will allow us to further validate the ctDNA findings observed in Phase 2 while generating molecular response data that will advance the understanding of treatment benefits for patients and strengthen the regulatory submission.”
This study adds to the evidence Natera continues to generate in head and neck cancer. The company recently announced a successful readout of the prospective Phase 2 SINERGY trial, supporting Signatera MRD-guided treatment in this histology.
“Growing evidence continues to demonstrate the value of Signatera MRD detection in head and neck cancer,” said Eric Matthews, general manager, biopharma, Natera. “We’re pleased to partner with Aveta on AVTA 30-01 to demonstrate how Signatera has the potential to advance the field and improve care for patients.”
References
Sun H, et al. Global burden of head and neck cancer: Epidemiological transitions, inequities, and projections to 2050. Front Oncol. 2025 Sep 25;15:1665019.About Natera
Natera™ is a global leader in cell-free DNA and precision medicine, dedicated to oncology, women’s health, and organ health. We aim to make personalized genetic testing and diagnostics part of the standard-of-care to protect health and inform earlier, more targeted interventions that help lead to longer, healthier lives. Natera’s tests are supported by more than 400 peer-reviewed publications that demonstrate excellent performance. Natera operates ISO 13485-certified and CAP-accredited laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) in Austin, Texas, and San Carlos, California, and through Foresight Diagnostics, its subsidiary, operates an ISO 27001-certified and CAP-accredited laboratory certified under CLIA in Boulder, Colorado. For more information, visit www.natera.com.
About Aveta Biomics
Aveta Biomics is a clinical-stage immuno-oncology company advancing first-in-class oral therapies designed to reprogram the tumor microenvironment and expand the benefits of immunotherapy to patients with immune-cold cancers. The company’s lead candidate, APG-157, has received FDA Fast Track and Orphan Drug Designations for head and neck squamous cell carcinoma and is in a global phase 3 registrational trial. APG-157 is also being evaluated across additional oncology indications including high-grade adult glioma and oral dysplasia. For more information, visit www.avetabiomics.com.
Forward-Looking Statements (for Natera)
All statements other than statements of historical facts contained in this press release are forward-looking statements and are not a representation that Natera’s plans, estimates, or expectations will be achieved. These forward-looking statements represent Natera’s expectations as of the date of this press release, and Natera disclaims any obligation to update the forward-looking statements. These forward-looking statements are subject to known and unknown risks and uncertainties that may cause actual results to differ materially, including with respect to our or our partners’ efforts to develop and commercialize new product offerings, whether the results of clinical or other studies will support the use of our product offerings, the impact of results of such studies, our expectations of the reliability, accuracy, and performance of our tests, or of the benefits of our tests and product offerings to patients, providers, and payers. Additional risks and uncertainties are discussed in greater detail in "Risk Factors" in Natera’s recent filings on Forms 10-K and 10-Q, and in other filings Natera makes with the SEC from time to time. These documents are available at www.natera.com/investors and www.sec.gov.
Forward-Looking Statements (for Aveta)
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements, including those regarding the impact of the Fast Track Designation, the progress of our clinical trials, potential regulatory approvals, the development and commercial success of our drug candidates, and our strategic goals, reflect our current expectations and involve risks and uncertainties. Actual results may differ materially due to factors such as our ability to advance drug candidates through development and regulatory approval, clinical trial outcomes, competition, and economic conditions. Words like “may,” “will,” “could,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” and similar expressions are intended to identify forward-looking statements. These statements are based on current expectations and are subject to risks and uncertainties that could cause actual results to differ materially. We caution you not to place undue reliance on these statements, which speak only as of the date they are made. As a private company, Aveta Biomics is under no obligation to publicly update or revise any forward-looking statements to reflect new information or future events, except as required by applicable law.
Trump koupil akcie Axon za až 5 milionů USD dva týdny předtím, než ICE požádala o pětiletou zakázku na Tasery za 220 milionů USD. Načasování vyvolalo otázky ohledně střetu zájmů.
President Donald Trump bought as much as $5 million in shares of Axon Enterprise — maker of Tasers, body cameras and policing software — two weeks before Immigration and Customs Enforcement sought a five-year, $220 million contract that experts told CNBC appeared tailored to the company's weapons.
On Feb. 10, Trump purchased between $1 million and $5 million worth of Axon stock, according to federal disclosures he filed in May. On Feb. 24, ICE posted a notice seeking roughly 17,800 new Tasers, along with unlimited cartridges and training.
The White House has said Trump's assets are held in a trust managed by his children and that Trump's investments are managed by independent third-party firms, not Trump or his family.
"There are no conflicts of interest," spokesperson Anna Kelly told CNBC, calling the scrutiny a "tired narrative" pushed by Democrats.
Trump's disclosures with the U.S. Office of Government Ethics, made public May 14, show more than 3,700 transactions, with the total amount for each listed as a range rather than an exact figure.
Under federal law, presidents are exempt from the criminal conflict-of-interest statute that applies to most executive branch officials.
The ICE notice does not name Axon, which makes about 90% of U.S. Tasers according to investment firm Brown Advisory, but it calls for "conductive-energy weapons" with specifications and capabilities that procurement reviewers and three policing experts told CNBC appeared to match only Axon products. The company already supplies the federal government with Tasers.
If finalized, the purchase would more than quadruple ICE's current Taser arsenal, replacing about 4,300 devices in the field, according to the February notice.
The notice refers to an upgrade to the "T10," Axon's "TASER 10" model, to replace ICE's older "X26P/X2 Tasers," which are also Axon-made. It also specifies features associated with "TASER 10," including a 45-foot range and 10 individually targeted probes — all specifications and capabilities that procurement experts say effectively foreclose other bidders.
There's no evidence Trump was involved in or had knowledge of the procurement process, that contracting officials knew of his stock purchase or that Axon knew that Trump was a shareholder. Trump bought the stock on Feb. 10, but the purchase did not become public until his financial disclosure was released in May. There is no indication Axon had access to non-public information about the president's personal investments.
The ICE notice was part of the standard federal procurement process. Federal procurement records show no contract has been awarded yet, and because the notice was a "Request For Information" rather than a formal solicitation, there is no public record showing which vendors, if any, responded.
Axon did not respond to requests for comment on whether it discussed the potential Taser purchase with ICE, DHS or White House officials before ICE posted the Feb. 24 notice.
The timing of the notice raises questions for ethics and three policing experts in part because of its proximity to Trump's stock purchase.
The president was also carrying out his pledge to enact mass deportations. Trump's Feb. 10 purchase occurred weeks after federal agents in Minneapolis shot and killed two U.S. citizens who were protesting an immigration crackdown in the city. Civil rights advocates have decried the killings of protesters as an overreach of law enforcement.
"What happened [in Minneapolis] showed how ICE agents have a hard job," said Deborah Fleischaker, a former acting chief of staff at ICE during the Biden administration. "The agency has a responsibility to make sure they have appropriate modern tools and training, but it's vital that new purchases are made for the right reasons."
Fleischaker, now a senior advisor for immigration policy and strategy at UnidosUS, said the timing "raises red flags," while cautioning it is impossible to assess from the public record whether anything improper occurred. UnidosUS is a nonprofit, nonpartisan Hispanic civil rights advocacy group.
"It is not smart to buy stock in a company that was impacted by the decisions you would be making at the agency," Fleischaker said. "I would have stayed far, far away from actual impropriety, or the appearance of impropriety."
Read more on Trump investmentsCompany that bet big on Trump-backed crypto says its fortunes have improvedTrump family got about $500M from crypto venture — but investors saw steep lossesTrump Jr. calls banking a 'Ponzi scheme' that forced family to create crypto businessThe Trump family crypto empire looks to Asia: Eric Trump talks Bitcoin in Hong KongTrump family says U.S. dollar needs an upgrade and they are the ones to do itEthics experts said the concern is not proof of wrongdoing, but the appearance of a conflict.
"The concern is that [Trump] bought into a company whose business could grow if his own administration expands immigration enforcement," Jordan Libowitz, vice president of communications at Citizens for Responsibility and Ethics in Washington, told CNBC. CREW is a liberal-leaning, nonpartisan watchdog group on government ethics.
Axon shares rose more than 22% in the month after Trump's purchase, before paring those gains. As of the June 26 close, the stock was up about 7% from his purchase date. If Trump bought near the top amount of the disclosed range, the potential paper gain could be worth roughly $350,000 as of market close on June 26. In the week following ICE's notice for seeking a contract, the company's stock rose more than 34%.
ICE and its parent agency, the Department of Homeland Security, did not respond to requests for comment. CNBC asked the agencies whether the purchase has been awarded, why ICE is seeking such a large expansion, how many vendors expressed interest, whether any company besides Axon could meet the requirements and whether the deal requires DHS secretary-level approval.
A person familiar with the procurement, who spoke on condition of anonymity due to fear of retaliation for discussing the pending ICE notice, said awarding the Taser contract appears to be stalled by its price tag and a shakeup in DHS leadership.
The person said ICE posted the contract notice about a week before then-Homeland Security Secretary Kristi Noem was fired and before she had signed off on it. Under Noem, DHS rules required expenditures over $100,000 to be personally approved by the secretary's office. Homeland Security Secretary Markwayne Mullin canceled the rule in April.
It's unclear what the timeline for awarding the contract is, but the person familiar with the procurement said DHS is expected to continue pursuing a deal.
Axon's growing federal footprintFor Axon, the financial upside may not stop at Tasers.
The roughly $35 billion company's biggest growth engine is the policing infrastructure that can follow weapons purchases: cloud storage, evidence-management systems, body cameras, real-time operations tools and AI products. Policing experts say one-time device orders can turn into a long-term technology relationship.
"If Trump expands ICE, Axon could be selling the infrastructure behind the crackdown," said Matthew Guariglia, a senior policy analyst at the Electronic Frontier Foundation focused on policing surveillance who has written extensively about Axon. "It can sell the cameras, cloud storage, software and AI tools that come with a bigger federal enforcement machine." The nonprofit group advocates for privacy and free speech online.
Axon already has a $370 million DHS body-camera and software contract awarded in 2023, though only about $67.5 million has been obligated so far, according to HigherGov, a government market-intelligence platform that tracks federal contracts and grants.
The potential ICE Taser deal would land as Axon is already riding record demand. The company reported its two highest-revenue quarters on record: $796.7 million in the fourth quarter of 2025, up 39% from a year earlier, and $807.3 million in the first quarter of 2026, up 34%, fueled by Taser sales and fast-growing AI products.
Axon executives told investors in February that DHS contracts are a "major opportunity."
Axon has been staffing up to chase that opening. On a May 6 earnings call, Axon President Joshua Isner said the company had "rebuilt a large portion" of its federal team and hired Claudia Davidson from Palantir, where she spent more than seven years helping expand the data-mining and defense contractor's business with federal agencies.
"We're seeing renewed interest in body cameras and Tasers in federal law enforcement," Isner told investors, adding that Axon's federal business was "trending very much in the right direction" and that, "with a few things going our way, it could be a banner year in Fed."
However, civil liberties advocates warn that ICE is wading deeper into Axon's surveillance ecosystem.
Axon's software works to combine live feeds from body cameras, drones, fixed cameras and other sources. If ICE expands raids and works more closely with state and local police, advocates warn that this kind of system could give federal agents a real-time map of local operations.
"If they are able to plug into Ring cameras, livestreams, body cameras and other local feeds, then suddenly you are not just talking about officer safety or accountability," Guariglia said. "You are talking about a platform that could give federal law enforcement a real-time picture of where people are, what is happening on the ground and how to respond with local precision."
Axon announced a Ring partnership in 2025 that lets Ring users voluntarily share footage with law enforcement through Axon's evidence platform. Axon's Fusus platform separately aggregates shared community cameras, body cameras, drones and other feeds onto a real-time map.
Fleischaker said the proposed Taser use expansion via the DHS contract appears consistent with the Trump administration's broader immigration agenda.
"It indicates what we know from other places, which is that the Trump administration has and will continue to ramp up immigration enforcement beyond levels we've ever seen," Fleischaker said. "That requires lots and lots of enforcement, and they would be procuring Tasers to be a part of that effort."
Politically connectedAxon's growth strategy has also led the company to boost its spending in Washington.
Axon spent nearly $2.5 million lobbying last year, its highest annual total, according to OpenSecrets, a nonprofit organization that tracks political spending. Its targets included legislation and regulation around body cameras, counter-drone technology, digital evidence management and other law-enforcement products it is pushing into federal agencies.
And that push appears to be gaining ground. Congress has proposed a $20 million line item in DHS appropriations requiring the agency to outfit immigration enforcement agents with body cameras, partly as a result of heavy lobbying by Axon, policing experts say.
Democrats have joined the effort, too. Sens. Ruben Gallego and Mark Kelly, both Arizona Democrats, introduced legislation requiring all DHS officers to wear body cameras. The legislation has no Republican support, making it unlikely to advance in the Republican-controlled Senate.
Donors connected to Scottsdale, Arizona-based Axon donated over $20,000 to Gallego during the 2024 election cycle when he ran for the Senate, according to OpenSecrets.
Gallego and Kelly, who have publicly championed body-camera and use-of-force requirements for ICE, did not respond to requests for comment on Axon's position as a likely beneficiary of body-camera mandates.
On Capitol Hill, Democrats have called for body cameras as an accountability measure and as a political bargaining chip with Republicans. For Axon, they are also a gateway product, policing experts say, to tie federal officers to its cloud storage, evidence software and AI tools.
"Body cameras can create a durable technology relationship with law enforcement agencies because the footage has to be stored, managed, analyzed and integrated into broader evidence systems," Guariglia said.
Axon's political spending has also drawn scrutiny from shareholders.
The Nathan Cummings Foundation sued Axon in January to stop the company from excluding a shareholder proposal seeking more disclosure around its political spending.
"Since Trump came into office, Axon has spent enormous amounts of money in politics to curry favor and support contracts and laws that benefit the company," Richard Kirby, a former SEC attorney who represented the foundation in its lawsuit against Axon that settled March 9, told CNBC. "That is exactly why investors need transparency."
Matador Resources oznámila, že její společnost San Mateo Midstream koupí provozní aktiva Cardinal Midstream za 752 milionů USD. Akvizice má rozšířit kapacitu zpracování plynu v Delaware Basin na více než 1 miliardu kubických stop denně.
DALLAS--(BUSINESS WIRE)--Matador Resources Company (NYSE: MTDR) (“Matador” or the “Company”) today announced that San Mateo Midstream, LLC (“San Mateo”), Matador’s 51%-owned midstream joint venture with Five Point Infrastructure (“Five Point”), has entered into a definitive agreement to acquire the operating subsidiaries of Cardinal Midstream Partners, LLC (“Cardinal”), a portfolio company of EnCap Flatrock Midstream, for total cash consideration of $752 million. The transaction is expected to close on or before July 31, 2026, subject to customary closing conditions (the “Cardinal Acquisition”). Matador anticipates the Cardinal Acquisition to be cash neutral for Matador as it expects to use distributions from San Mateo and/or proceeds from the potential drop-down to San Mateo or sale of a portion of Matador’s wholly-owned midstream assets to fund any required cash contributions to San Mateo related to the acquisition.
Cardinal Acquisition Highlights
Complementary Midstream Assets. Cardinal’s midstream assets are complementary to San Mateo’s existing natural gas gathering and processing system and provide San Mateo the ability to move natural gas more easily throughout the northern Delaware Basin in southeast New Mexico and West Texas (see map, Exhibit A). Cardinal’s assets consist of (i) a cryogenic natural gas processing plant complex in Loving County, Texas with a designed inlet capacity of approximately 320 million cubic feet of natural gas per day, and (ii) approximately 145 miles of low-pressure and high-pressure natural gas gathering pipelines located in West Texas and southern Eddy County, New Mexico. The Cardinal plant complex sits on approximately 75 acres with two residue natural gas takeaway connections and four natural gas liquids takeaway connections, providing San Mateo the ability to expand processing capacity in the future. Third-Party Customer Relationships and Volumes. Nine of Cardinal’s natural gas gathering and processing customers would be new natural gas customers for San Mateo. The mix of Cardinal’s major, mid-cap and private Delaware Basin producers is expected to directly increase San Mateo’s customer base, volume throughput and revenue generation from third-party customers. Expanded Scale. The Cardinal Acquisition is expected to increase San Mateo’s designed natural gas processing capacity to more than one billion cubic feet per day and expand San Mateo’s gathering systems to over 800 miles of pipeline. Enhanced Flow Assurance for Matador and Other Customers. The combined natural gas system is expected to provide immediate synergies for San Mateo’s gas gathering and processing system. These expected synergies include the ability to flow volumes between Cardinal’s natural gas processing plant in Loving County, Texas and San Mateo’s existing Marlan Processing Plant and Black River Processing Plant, both located in Eddy County, New Mexico. Once acquired, the Cardinal plant complex in Texas as shown on the map should provide additional options and coverage to producers in the area. Accretive to Adjusted EBITDA and Cash Flows. San Mateo expects the Cardinal assets to be immediately accretive to both San Mateo’s Adjusted EBITDA and cash flows. Adjusted EBITDA from the Cardinal assets is expected to increase to up to $110 million on an annualized basis by 2028 when the Cardinal plant complex is anticipated to be completely full. Financing Highlights
San Mateo expects to finance the Cardinal Acquisition, in part, through a new term loan of up to $650 million under its existing credit facility. This new term loan will be led by PNC Bank, the lead bank under Matador’s reserves-based credit facility, and Truist Bank, the lead bank under San Mateo’s existing credit facility. The new term loan will become due and payable 364 days following the closing of the Cardinal Acquisition. The remainder of the purchase price is expected to be funded through a combination of cash on hand, borrowings under San Mateo’s existing credit facility and capital contributions from its partners. Matador expects to use distributions from San Mateo and/or proceeds from the potential drop-down to San Mateo or sale of a portion of Matador’s wholly-owned midstream assets to fund any cash contribution.
Management Comments
Joseph Wm. Foran, Matador’s Founder, Chairman and CEO and San Mateo’s Founder, commented, “We are very pleased to announce San Mateo’s acquisition of Cardinal Midstream. We believe the acquisition—which is being funded by midstream—is the next step in the growth of San Mateo and a continuation of the strategic vision Matador and Five Point share for our joint midstream business to be a leading midstream company in the Delaware Basin, providing flow assurance to Matador and third-party customers. This transaction was built on relationships. Matador’s relationship with the EnCap Investments L.P. (“EnCap”) team and its affiliated entities goes back decades. We look forward to welcoming and building relationships with Cardinal’s customers and working with the talented Cardinal operating team.
“We believe this acquisition will provide substantial benefits to Matador, Cardinal and San Mateo and their respective stakeholders. Financially, this acquisition is expected to add immediate third-party volumes and cash flows, enhancing both San Mateo’s and Cardinal’s expected outlook for 2026 and beyond. This increased scale further improves San Mateo’s positioning for potential strategic alternatives at the corporate level. Strategically, the Cardinal system effectively “completes the circle” for San Mateo infrastructure in the Delaware Basin. Connecting Cardinal’s natural gas gathering and processing assets to San Mateo’s existing natural gas system is expected to give San Mateo the ability to move natural gas throughout the northern Delaware Basin—north to south or south to north—creating better flow assurance and system flexibility that we believe few midstream providers can match.
“The Cardinal Acquisition is expected to not only provide strategically increased flow assurance to Cardinal’s customers but also to provide natural gas processing for Matador’s development of its recently acquired federal lease acreage in Lea County, New Mexico. Additionally, because Cardinal’s system extends near Matador’s Wolf asset area in Loving County, Texas, San Mateo will be well positioned to provide flow assurance for volumes from this asset area too.
“It is also important to note that “midstream money is being used to fund midstream acquisitions” as any capital contributions from Matador to San Mateo are expected to be paid with either cash distributions from San Mateo and/or proceeds received from the potential drop-down to San Mateo or sale of Matador’s wholly-owned midstream assets. These wholly-owned midstream assets continue to provide critical flow assurance for Matador’s natural gas, oil and water in Matador’s Ameredev area and other locations in Lea County, New Mexico.
“We also express our appreciation to PNC Bank and Truist Bank for their continued support and to each of San Mateo’s lenders that we anticipate participating in the new term loan. This new term loan is expected to effectively provide a bridge to San Mateo’s potential future strategic transactions.
“As we have noted before, San Mateo began as a startup midstream company in 2017 and has grown into one of the premier midstream businesses in the northern Delaware Basin and one of the only midstream companies that provides integrated services for all three streams—natural gas, oil and water. We believe the addition of Cardinal will position San Mateo for its next chapter of growth.”
Advisors
Baker Botts L.L.P., led by Preston Bernhisel, and O’Melveny & Myers LLP, led by Jason Schumacher, acted as counsel to San Mateo on the Cardinal Acquisition. Willkie Farr & Gallagher LLP, led by Nathan Meredith, acted as counsel to Cardinal on the acquisition.
About Matador Resources Company
Matador is an independent energy company engaged in the exploration, development, production and acquisition of oil and natural gas resources in the United States, with an emphasis on oil and natural gas shale and other unconventional plays. Its current operations are focused primarily on the oil and liquids-rich portion of the Wolfcamp and Bone Spring plays in the Delaware Basin in Southeast New Mexico and West Texas. Matador also operates in the Haynesville shale and Cotton Valley plays in Northwest Louisiana. Additionally, Matador conducts midstream operations in support of its exploration, development and production operations and provides natural gas processing, oil transportation services, natural gas, oil and produced water gathering services and produced water disposal services to third parties.
For more information, visit Matador Resources Company at www.matadorresources.com.
About San Mateo Midstream, LLC
San Mateo is a midstream joint venture owned 51% by Matador and 49% by an affiliate of Five Point Infrastructure LLC. San Mateo provides natural gas gathering, treating and processing, produced water gathering and disposal, and oil gathering and transportation services to Matador and third-party customers in the Delaware Basin in Southeast New Mexico and West Texas.
Forward-Looking Statements
This press release includes “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. “Forward-looking statements” are statements related to future, not past, events. Forward-looking statements are based on current expectations and include any statement that does not directly relate to a current or historical fact. In this context, forward-looking statements often address expected future business and financial performance, and often contain words such as “could,” “believe,” “would,” “anticipate,” “intend,” “estimate,” “expect,” “may,” “should,” “continue,” “plan,” “predict,” “potential,” “project,” “hypothetical,” “forecasted” and similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain such identifying words. Such forward-looking statements include, but are not limited to, statements regarding the anticipated timing and closing of the Cardinal Acquisition; the expected benefits, opportunities and results of the Cardinal Acquisition, including the expected impact on cash flows and Adjusted EBITDA, third-party volumes, system connectivity, flow assurance, expansion opportunities and other anticipated impacts of the Cardinal Acquisition; the anticipated financing of the Cardinal Acquisition, including any bridge term loan or other financing transaction, or the required capital contributions or sources thereof, including any potential drop-down to San Mateo or sale of Matador’s wholly-owned midstream assets; other aspects of the Cardinal Acquisition, including guidance, projected or forecasted financial and operating results, future liquidity and the payment of distributions; and San Mateo’s future growth and potential strategic alternatives. Actual results and future events could differ materially from those anticipated in such statements, and such forward-looking statements may not prove to be accurate. These forward-looking statements involve certain risks and uncertainties, including, but not limited to, the satisfaction of closing conditions for the Cardinal Acquisition; the possibility that the Cardinal Acquisition may not close on the anticipated timeline or at all; the ability of San Mateo to integrate the Cardinal assets and realize the anticipated benefits of the Cardinal Acquisition; the availability and terms of financing; commodity price volatility; operational risks; regulatory changes; risks related to obtaining the requisite regulatory approvals for the Cardinal Acquisition; disruption from the Cardinal Acquisition making it more difficult to maintain business and operational relationships; significant transaction costs associated with the Cardinal Acquisition; the risk of litigation and/or regulatory actions related to the Cardinal Acquisition, as well as the other factors that could cause actual results to differ materially from those anticipated or implied in the forward-looking statements. For further discussions of risks and uncertainties, you should refer to Matador’s filings with the Securities and Exchange Commission (“SEC”), including the “Risk Factors” section of Matador’s most recent Annual Report on Form 10-K and any subsequent Quarterly Reports on Form 10-Q. Matador undertakes no obligation to update these forward-looking statements to reflect events or circumstances occurring after the date of this press release, except as required by law, including the securities laws of the United States and the rules and regulations of the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. All forward-looking statements are qualified in their entirety by this cautionary statement.
(1) Adjusted EBITDA is a non-GAAP financial measure. Matador and San Mateo define Adjusted EBITDA as earnings before interest expense, income taxes, depletion, depreciation and amortization, accretion of asset retirement obligations, unrealized derivative gains and losses, non-recurring transaction costs for certain acquisitions, non-cash stock-based compensation expense, loss on debt extinguishment, net gain or loss on asset sales and impairments and certain other non-cash items. The most comparable GAAP measures to Adjusted EBITDA are net income or net cash provided by operating activities. Estimated Adjusted EBITDA attributable to the Cardinal assets is presented on an asset-level basis and reflects earnings before interest expense, income taxes, depreciation, depletion, amortization and certain other non-cash or non-recurring items. Matador and San Mateo are unable to provide a reconciliation of this forward-looking non-GAAP financial measure to the most directly comparable GAAP measure without unreasonable effort due to the inherent difficulty in forecasting certain reconciling items.
Acuity uvedla, že poptávka po osvětlení po zimním oslabení sílí a projektový tok se normalizuje směrem ke 4. čtvrtletí. Tržby AIS vzrostly o 14,9 % na 303,5 mil. USD.
Key Takeaways AYI said lighting demand is firming after winter softness, with project flow normalizing into Q4.AIS sales rose 14.9% to $303.5 million, driven by Distech, QSC and open-architecture wins.Acuity cited AIS product launches, data center momentum and organic growth in controllers. Acuity Inc. (AYI - Free Report) used its third-quarter fiscal 2026 earnings call to press a forward-looking message: lighting demand is stabilizing, while Acuity Intelligent Spaces continues to supply the company’s faster-growth engine. Management emphasized execution more than headline beat metrics.
That framing mattered because the quarter again showed a split business. Lighting remained pressured on sales, but AIS expanded at a double-digit rate, and management sounded increasingly confident about growth avenues in controls, OEM channels and data centers.
AYI Sees a Better Setup in LightingChairman, president and CEO Neil Ashe said Acuity Brands Lighting is seeing firmer demand after a softer stretch in the winter months, when conversion rates from quoting to releases ran longer than normal. He said activity is starting to normalize and described project flow as more typical heading into the fourth quarter.
Chief financial officer Karen Holcom added that fourth-quarter sales should rise sequentially from the third quarter, though not necessarily at the same pace as the recent step-up. That outlook stopped short of a broad rebound call, but it marked a more constructive tone than earlier commentary around a tepid market.
The quarter itself still reflected pressure. ABL sales fell 1.9% to $905.2 million, though adjusted operating margin remained a healthy 18.2%. Management tied the sales decline partly to a tough comparison against last year’s tariff-related order pull-forward rather than to a new deterioration in demand.
Acuity Leans Harder on AIS GrowthIf the call had a central growth theme, it was AIS. Sales in the segment climbed 14.9% to $303.5 million, with adjusted operating profit up 22.5% and adjusted operating margin reaching 25.1%, driven by Distech and QSC.
Ashe spent much of his prepared remarks on Distech, arguing that Acuity’s open-architecture strategy is translating into share gains. He cited wins at universities, sports venues, enterprise campuses and data centers while also pointing to OEM manufacturers adopting the Eclipse portfolio for next-generation applications.
Management also highlighted new product cadence inside AIS, including Eclipse Resilience for mission-critical cooling and a preloaded dashboard tied to occupancy and space utilization. The message was that AIS is broadening from controls into a platform story built around edge control, cloud intelligence and occupant experience.
AYI Protects Margins While InvestingThe company’s financial backdrop supported that strategy. Adjusted earnings per share increased to $5.31 from $5.12 a year earlier. The figure topped the Zacks Consensus Estimate of $5.20 by 2.1%. Net sales rose 1.6% to $1.2 billion, which modestly beat the $1.19 billion estimate by 1.1%.
Gross margin remained a notable talking point. Adjusted gross profit margin improved 10 basis points to 50.1%, helped by a richer AIS mix, even as ABL adjusted gross margin slipped 50 basis points to 46.1%.
Ashe said inflation remains present across materials and SG&A, with medical costs one example, but he stressed that recent spending has been concentrated in technology and AI capabilities rather than undisciplined overhead growth. He argued that those investments are already helping gross margin and should create stronger operating leverage when volume improves.
Acuity Keeps Capital Deployment FlexibleHolcom said Acuity’s capital allocation priorities have not changed: invest for growth, raise the dividend, pursue acquisitions and repurchase stock opportunistically. That framework was visible in the quarter’s actions.
For the first nine months of fiscal 2026, Acuity generated $520.2 million in operating cash flow and $461.7 million in free cash flow. It also repaid $200 million of term debt year to date, repurchased about 766,000 shares for $230 million and refinanced its revolver with a new five-year $800 million unsecured facility.
Ashe made clear that acquisitions remain a priority, especially in AIS. But he also underscored selectivity, pointing to QSC as the model for buying quality assets that can perform better inside Acuity’s broader platform.
AYI Uses Q&A to Expand the Data Center StoryAnalyst questions pushed management to define how durable AIS growth is and whether data centers are becoming a more material opportunity. Ashe responded by tying recent momentum to a mix of product innovation, market share gains and expansion into adjacencies such as refrigeration and OEM channels.
On data centers, management sounded more explicit than in prior calls. Ashe said Distech now has both direct digital controllers and PLC controllers, which broadens its ability to serve hyperscalers, while the lighting side is also seeing rapid percentage growth off a smaller base.
The answer that stood out most was management’s insistence that this push is currently organic. Ashe said the company’s entry into the data center market is being driven by internal product development, not by a need to buy its way in.
Acuity Leaves the Call With a Clearer ToneThe call ended with a more confident posture than the raw ABL sales number alone would imply. Management’s emphasis was on normalization in lighting, continued margin discipline and a wider runway for AIS.
Ashe also pointed to internal priorities that framed Acuity’s next phase: deploying AI inside the business, accelerating product velocity, improving digital manufacturing and pursuing targeted AIS expansion. Those comments reinforced a company trying to compound operational discipline with higher-value technology exposure.
Zacks Signals Still Call for SelectivityAYI currently carries a Zacks Rank #3 (Hold), alongside Value and Growth Scores of B, a Momentum Score of F and a VGM Score of C. Under the Zacks framework, a Zacks Rank #1 (Strong Buy) and #2 (Buy) stocks paired with Style Scores of A or B offer the strongest near-term setup, while a Rank #3 is generally more neutral. You can see the complete list of today’s Zacks #1 Rank stocks here.
That mix points to a stock with some supportive value and growth characteristics, but weaker momentum. The Zacks methodology also treats estimate revisions as the primary driver, which means the current rank can change after analysts update forecasts following the quarter.
Arthur Hayes podpořil Hypercall od Synapse Protocol jako rivala Deribitu a koupil 6,16 milionu tokenů SYN v hodnotě 2,2 milionu dolarů. Token poté vyskočil o 26 % za poslední 2 hodiny.
BitMEX co-founder Arthur Hayes expressed his support behind Synapse Protocol’s Hypercall options DEX, claiming it as a rival to Deribit. Hayes also purchased SYN token, triggering a 26% over the past 24 hours.
Arthur Hayes Sees Synapse’s Hypercall as Deribit Rival In an X post on June 29, BitMEX co-founder highlighted Hypercall, a options DEX built by the Synapse team and settled on Hyperliquid. He believes the platform can compete with crypto derivatives trading exchange Deribit.
“I still want to be long the Hyperliquid ecosystem but I need some asymmetry. It’s time for an options dex to properly take on Deribit,” said Arthur Hayes.
In addition, Arthur Hayes highlighted several factors including low FDV of $81 million, no venture capital overhang or unlocks, 88% of circulating supply with the remaining in treasury, and listed on major exchanges like Binance and Kraken.
He drew parallels to his earlier successful call on Hyperliquid’s HYPE token, calling SYN one of the most asymmetric bets in crypto. Notably, Hypercall also extends the utility of SYN token, which benefits from revenue mechanisms such as buybacks.
SYN Token Price Surges 26% SYN token surged 26% over the past 2 hours after Arthur Hayes said he found “this pretty compelling. On-chain data also revealed he purchased 6.16 million SYN tokens worth $2.2 million from Flowdesk.
While SYN price pared 12% gains, Arthur Hayes is still sitting at a profit. He bought the token at a price of $0.3573.
Synapse token has rallied more than 1,100% in a month. The token recorded a massive rally when the broader crypto market crashed. The move fits Arthur Hayes’ focus on the Hyperliquid ecosystem.
Derivatives data signaled massive profit booking in the last few hours amid “buy the rumor, sell the news” strategy. SYN futures open interest is down 13% in past 4 hours at $31.98 million, but still up 5% over past 24 hours.
Notably, SYN futures open interest plunged 15% on Binance, over 14% on Bitget, and 10% on MEXC. This indicates selling pressure on the token as many used the latest liquidity to exit the token.
Korn Ferry uzavřela definitivní dohodu o převzetí AMS za zhruba 850 milionů GBP. Spojením vznikne globální lídr v talentovém a organizačním poradenství.
LOS ANGELES--(BUSINESS WIRE)--Korn Ferry (NYSE: KFY), a global organizational consulting firm, today announced that it has entered into a definitive agreement with OMERS Private Equity to acquire UK-headquartered AMS, which will create a global leader in talent and organizational consulting.
The combination will bring together two highly complementary organizations across geographies and industries with a shared commitment to drive business performance. Following completion, the collective firm will have more than 16,000 colleagues placing a professional in a job approximately every 90 seconds.
“By bringing AMS into the Korn Ferry family, we are expanding our ability to help clients solve their most critical organizational challenges,” said Gary D. Burnison, CEO, Korn Ferry. “Despite all of the technological innovations of yesterday, today and tomorrow, the real driver of organizational success is people. And with our AMS colleagues we will be stronger together than apart. Over almost 20 years I have watched AMS grow and evolve, with deep admiration and respect. I am convinced that the culture and values of both companies are completely aligned. And it all starts with people. This is indeed a significant milestone for Korn Ferry and I am excited about the future that we will shape together.”
The transaction will combine Korn Ferry’s expertise across Search, Talent & Organizational Solutions, and Workforce Solutions with AMS’s highly regarded expertise in Recruitment Process Outsourcing (RPO), Early Careers and Campus Recruiting, Contingent Workforce Solutions, Consulting, and Skills Creation.
“At AMS we connect organizations with the people who advance their vision and deliver their purpose—powering industries, achieving results and shaping futures,” said Rosaleen Blair, Founder and Chair of AMS. “In Korn Ferry we have a like-minded partner that shares the same beliefs and embraces the same values.” Following the consummation of the transaction, Rosaleen Blair will continue in a Chair role.
“Combining AMS with Korn Ferry will create new opportunities for our clients, our teams, and accelerate our ability to shape the future of work,” said Gordon Stuart, CEO of AMS.
“AMS has made incredible progress over the course of our ownership,” said Michael Block, Head of Private Capital, OMERS. “We have supported the company as it has expanded its capabilities, strengthened its client relationships and focused on the people and organizations it serves. Korn Ferry is a strong strategic fit for AMS as it enters its next chapter.”
Founded by Rosaleen Blair in 1996, AMS serves many of the world’s leading organizations across financial services, technology, healthcare, life sciences, consumer, industrial, and public sector markets. Its operations span more than 120 countries, including a well-established presence throughout Europe and Asia.
Drawing on the totality and strength of both firms—and leveraging combined expertise and relationships across geographies, the combined company will create more sustainable opportunities at scale.
Terms of the Acquisition Agreement
Under the terms of the acquisition agreement, Korn Ferry has agreed to acquire AMS for an aggregate purchase price of approximately £850 million (approximately $1.1 billion), consisting of (i) approximately £659 million (approximately $881 million) in cash and (ii) approximately £191 million (approximately $255 million) in Korn Ferry common stock.1
Korn Ferry expects to fund the cash portion of the transaction consideration with approximately $300 million of cash on hand and the remaining approximately $581 million of cash consideration with borrowings under Korn Ferry’s existing revolver. Additionally, Korn Ferry will issue approximately 3.6 million shares2, subject to a 15% collar at the closing.
On a current annual run-rate basis, AMS is generating approximately $650 million of Fee Revenue and $100 million of Adjusted EBITDA.3 Assuming no adverse change in the economic environment, Korn Ferry estimates that the run-rate Adjusted EBITDA3 contribution within a year following the closing of the acquisition will be approximately $140 million.
The consummation of the transaction is subject to receipt of regulatory clearances and is expected to close in Korn Ferry’s 2nd fiscal quarter of FY’27. The transaction is expected to be immediately accretive to earnings per share in the first full year after adjusting for restructuring and integration and transaction costs.
AMS’s long-term contracts will add more than $1.5 billion in estimated fees remaining under existing contracts, providing greater revenue visibility and enhancing the Company’s ability to provide scalable, data-driven talent strategies across geographies and industries.
Additional details regarding the transaction will be discussed during a conference call with investors on Monday, June 29 at 8:30 a.m. EDT. The call will be webcast and available online at www.kornferry.com under Investor Relations, News & Events.
About Korn Ferry
Korn Ferry is a global consulting firm that powers performance. We unlock the potential in your people and unleash transformation across your business—synchronizing strategy, operations, and talent to accelerate performance, fuel growth, and inspire a legacy of change. That’s why the world’s most forward-thinking companies across every major industry turn to us—for a shared commitment to lasting impact and the bold ambition to Be More Than.
As the Official Talent & Organizational Consulting Partner of LA28, Korn Ferry is powering the nearly 5,000 people who power the Olympic Games—bringing in the right talent, building strong leaders, and shaping the structure and culture that will deliver an unforgettable experience for the world.
About AMS
We are people experts.
Our 8,000 colleagues power talent acquisition and consulting strategies that deliver results for leading organizations across 120 countries.
We partner with our clients to help re-define a new era of talent, driven by people, process, data and technology, enabling them to attract and retain the talent they need to achieve their vision.
Our core areas of service include: Recruitment Process Outsourcing (RPO), Early Careers and Campus Recruiting, Contingent Workforce Solutions, Consulting and Skills Creation, which are amplified by digital capability and strategic technology partnerships.
We call this...People powered partnership.
Forward-Looking Statements
Statements in this press release and our conference call include “forward-looking statements” within the meaning of the “safe harbor” provisions of the United States Private Securities Litigation Reform Act of 1995 concerning the transaction. Forward-looking statements may be identified by the use of words such as “anticipate,” “believe,” “expect,” “estimate,” “may,” “plan,” “outlook,” “project,” “will” or other similar expressions. Such forward-looking statements include, but are not limited to, statements relating to the USD converted purchase price, the number of shares of Korn Ferry stock to be issued in the transaction, the timing of the transaction, the expected benefits of the transaction, including the global leadership position of the combined company, the combined company’s expanded capabilities, transaction synergies, future financial and operating results, and the combined company’s plans, objectives and expectations. A number of factors could cause actual results or outcomes to differ materially from those indicated by such forward-looking statements. Such risks and uncertainties, many of which are outside of the control of Korn Ferry, include, but are not limited to: (1) the occurrence of any event or change that could give rise to the termination of the acquisition agreement; (2) the inability to timely complete or complete at all the transaction; (3) delays in obtaining or the inability to obtain, necessary regulatory approvals; (4) the risk that the transaction disrupts current plans and operations of Korn Ferry and/or AMS; (5) the ability to successfully integrate the operations and employees of AMS into Korn Ferry; (6) the ability to recognize the anticipated benefits of the transaction which may be affected by, among other things, the ability of Korn Ferry and AMS (prior to the closing) and the combined company (following the closing) to maintain relationships with clients and suppliers and retain key employees; (7) currency exchange rates; (8) fluctuations in Korn Ferry’s stock price; (9) costs related to the transaction; (10) the outcome of any legal proceedings that may be instituted against Korn Ferry or AMS or their respective affiliates following announcement of the transaction; (11) the possibility that Korn Ferry or AMS may be adversely affected by economic, business, and/or competitive factors; and (12) other risks and uncertainties indicated from time to time in filings with the SEC by Korn Ferry. Korn Ferry undertakes no obligation to update or revise the forward-looking statements, whether as a result of new information, future events or otherwise.
No Offer or Solicitation
This communication is not intended to and shall not constitute an offer to sell or the solicitation of an offer to sell or the solicitation of an offer to buy any securities.
Alphabet klesl o dvouciferné procento v posledních týdnech, ale Warren Buffett a Greg Abel zůstávají klidní. Firma dál zvyšuje investice do AI infrastruktury a poptávka po ní je podle ní rekordní.
Last year, Warren Buffett corrected one of his previous investing mistakes. He initiated a sizable position in Google parent Alphabet (GOOG 2.15%) (GOOGL 1.73%), several years after admitting that he regretted not buying the stock earlier.
After Buffett stepped down as Berkshire Hathaway's (BRKA +1.60%) (BRKB +2.08%) CEO at the end of 2025, his successor, Greg Abel, more than tripled the conglomerate's stake in Alphabet. The stock now ranks as Berkshire's fifth-largest holding.
But Google's stock has fallen by double digits over the past few weeks. Are Buffett and Abel worried that they made a mistake buying the stock? I don't think so. If you own shares of Alphabet, here's why you shouldn't be worried, either.
Image source: Getty Images.
Why the stock's decline isn't really scary Three factors explain Alphabet's decline since May. None of them should be scary to investors, in my opinion.
First, Alphabet's first-quarter update revealed another significant increase in planned capital expenditures. The company provided capex guidance of $180 billion to $190 billion for full-year 2026. Some investors have become jittery over the sky-high spending on artificial intelligence (AI) infrastructure by Alphabet and other tech giants.
Second (and related to the first factor), Alphabet announced in June that it was raising $80 billion through private placement equity offerings. The company said that these offerings are part of the plan "to fund investments in its world-class AI compute infrastructure to meet its unprecedented customer demand."
Third, two high-profile defections last week caused the stock to experience its worst day in more than a year. Noam Shazeer, Google's vice president of engineering and one of the leaders of the Gemini AI models, announced he was leaving to join OpenAI. Two days later, Google DeepMind vice president and engineering fellow John Jumper announced that he was leaving to join Anthropic. Jumper received a Nobel Prize with Google DeepMind CEO Demis Hassabis for developing AlphaFold, an AI system that predicts protein structures.
Anat Askkenazi, CFO of Alphabet and Google, said in the Q1 update that the company continues to see "unprecedented internal and external demand for AI compute resources." Ashkenazi pointed out that investments in AI infrastructure are driving record revenue and backlog growth.
What about the departures of key AI leaders? It is somewhat concerning. However, this kind of musical chairs is commonplace in the industry. Alphabet still has a huge level of AI talent and the money to recruit more people.
Today's Change
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I have no doubt whatsoever that neither Buffett nor Abel is losing sleep over the factors behind Alphabet's recent sell-off. For one thing, Abel led the charge for Berkshire's additional $10 billion investment in Alphabet that was part of the private placement. If he had any qualms about Alphabet spending more on AI infrastructure, he would never have committed such a significant amount of Berkshire's capital.
It's important to remember Buffett's perspective on stock declines. At Berkshire Hathaway's 2010 annual shareholder meeting, he said, "If you have a temperament that when others are fearful you're going to get scared yourself, you know, you are not going to make a lot of money in securities over time, in all probability."
What's more, the legendary investor gave a decidedly contrarian opinion. He stated that some investors buy a stock and then "think if it goes up it's wonderful, and if it goes down it's bad." Buffett explained, "We think just the opposite. When it goes down, we love it, because we'll buy more. And if it goes up, it kills us to buy more."
An opportunity for long-term investors As usual, Buffett was right. A pullback in a wonderful company's share price presents an excellent buying opportunity for long-term investors. And Alphabet remains a wonderful company.
The record Google Cloud backlog provides excellent revenue visibility. Google Search continues to grow, with generative AI serving as a tailwind rather than the "Google killer" some predicted. Waymo is the leader in autonomous ride-hailing. Alphabet is even now part of the Dow Jones Industrial Average (^DJI 0.09%), reflecting how important it has become to the U.S. economy.
Don't be surprised if Berkshire's next 13-F filing reveals that the conglomerate took advantage of Alphabet's decline to load up on more shares. After all, that's the Warren Buffett way.
Nvidia rozšiřuje tým pro Space-1, svůj první výpočetní systém pro vesmír. Nová role má pomoci vytvořit software pro orbitální datová centra a provoz na nízké oběžné dráze.
Nvidia CEO Jensen Huang. Bloomberg/Getty Images Nvidia's AI ambitions are officially out of this world this year, and they haven't come back down to Earth.
The AI chip giant is adding to the team behind Space-1, its first computing system designed for space. In recent weeks, the chip giant posted a second job tied to orbital data centers.
The role — for a system software principal architect — will help build software for Space-1, which the chip giant unveiled at its GTC event in March.
Space data centers have emerged as a potential way to get around growing constraints on land, power, and cooling on Earth. Companies like SpaceX are racing to make the idea a reality, while skeptics argue the costs still outweigh the benefits.
During a recent earnings call, Nvidia CEO Jensen Huang said the economics around space computing are poor today but will improve over time.
The principal architect job post follows another role shared earlier this year for an orbital data center system architect. While that position focuses on designing the overall system — from computing hardware to satellites to connectivity systems — the new post focuses on making Space-1's software work in practice.
The person hired will design the software that runs the system so it can withstand radiation and extreme temperature swings and be managed remotely.
Space-1 harnesses Nvidia's latest Vera Rubin AI chip platform and is designed for low-Earth orbit missions.
The system software role requires previous experience building AI infrastructure and systems in space. It offers a base salary of $272,000 to $431,250, which doesn't include Nvidia's coveted equity awards.
While the technology is still in its early stages, Nvidia's latest job postings suggest the chipmaker is moving from conceptual planning to building the systems needed to make it work.
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Geoff Weiss is a senior reporter on Business Insider’s tech team, where he writes about AI startups and Y Combinator, the intersection of AI and the media industry, and workplace dynamics within top AI labs and chip companies.Previously, Geoff was on the media desk, covering YouTube and Netflix, and themes like the intersection of Hollywood and the creator economy. His work on Netflix’s video podcasting ambitions and Mr Beast’s lessons for Hollywood won second and first prize, respectively, at the 2025 LA Press Club Awards.Prior to joining Business Insider, Geoff was the senior editor of Tubefilter and a staff writer at Entrepreneur. He graduated from New York University with a degree in English Literature.He can be reached at [email protected], on Signal @geoffweiss.25, and on LinkedIn. Have a tip? Use a personal email address and a nonwork device; here's our guide to sharing information securely.Selected stories:Nvidia crushed its quarter — and CEO Jensen Huang said in a leaked all-hands that 'the market did not appreciate it'Nvidia will foot the bill for Trump's new visa fees. Here's what CEO Jensen Huang told staff.Massive AI salaries and RTO are fueling a real estate boom in San Francisco: 'It's going to rain money'The AI talent wars are ricocheting across startups. Here's how they're competing with Big Tech.
AbbVie oznámila, že CHMP vydal kladné stanovisko k upadacitinibu (RINVOQ) pro léčbu dospělých a dospívajících s těžkou alopecií areata. Konečné rozhodnutí Evropské komise se očekává v příštích měsících.
Positive CHMP opinion is supported by data from the Phase 3 UP-AA clinical program in which upadacitinib achieved the primary endpoint of Severity of Alopecia Tool (SALT) score ≤ 20 and key secondary endpoints, including improvements in eyebrows and eyelashes, at week 241,2 Upadacitinib is the first JAK inhibitor to meet the stringent ranked secondary endpoint of complete scalp hair regrowth (SALT = 0) at week 241,2 , /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the approval of upadacitinib (RINVOQ®; 15 mg and 30 mg, once daily) for the treatment of adult and adolescent patients with severe alopecia areata (AA). The final European Commission decision is expected in the coming months.
"Alopecia areata is an unpredictable autoimmune disease with underrecognized patient burden," said Roopal Thakkar, M.D., executive vice president, research and development, chief scientific officer, AbbVie. "The CHMP's positive opinion for upadacitinib is a step closer to bringing a new treatment option to patients living with severe alopecia areata."
The CHMP positive opinion is supported by data from the ongoing Phase 3 UP-AA clinical program (M23-716), which includes two replicate, randomized, placebo-controlled, double-blind studies evaluating the efficacy and safety of upadacitinib in adult and adolescent patients with severe alopecia areata. Both the 15 mg and 30 mg doses of upadacitinib in each study met the primary endpoint of SALT score ≤ 20 at week 24, with significantly more patients achieving ≥ 80% scalp hair coverage compared with placebo. Key secondary endpoints were also met for both doses in both studies, including complete scalp hair regrowth (SALT = 0) at week 24. The safety profile of both doses of upadacitinib in Period A was generally consistent with that observed in approved indications.1,2
Upadacitinib is approved in the European Union (EU) for the treatment of adults and adolescents with atopic dermatitis, and adults with radiographic axial spondylarthritis, non-radiographic axial spondylarthritis, psoriatic arthritis, rheumatoid arthritis, ulcerative colitis, Crohn's disease, and giant cell arteritis. Use of upadacitinib in AA is not currently approved in the EU.
About Alopecia Areata
Alopecia areata (AA) is an unpredictable autoimmune disease causing a range of hair loss patterns, from sudden, round bald patches on the scalp to complete loss of all body hair, including scalp, face, eyebrows and eyelashes.3,4 Despite its immune-mediated nature, AA is often considered a cosmetic problem, which can lead to stigma and have an impact on patients' lives.5,6
About UP-AA Clinical Trial
UP-AA M23-716 was conducted as a single protocol that includes two replicate pivotal studies (Study 1 and Study 2) with randomization, investigative sites, data collection, analysis and reporting independent for each study. The Phase 3 randomized, placebo-controlled, double-blind studies evaluate efficacy and safety of upadacitinib in adult and adolescent subjects with severe alopecia areata. In Study 1 and Study 2 Period A, participants are randomized to one of three groups to receive upadacitinib 15 mg, upadacitinib 30 mg or placebo for 24 weeks. In Study 1 and Study 2 Period B, participants originally randomized to upadacitinib dose groups in Period A will continue their same treatment in Period B for 28 weeks. Participants originally randomized to placebo in Period A will either remain on placebo in Period B, or be randomized in one of two groups, based on their SALT score at week 24. In total, Study 1 and Study 2 Periods A and B span 52 weeks. Participants who complete Study 1 or Study 2 can join Study 3 and may be re-randomized to receive 1 of 2 doses of upadacitinib for up to 108 weeks. The two trials randomized 1,399 participants with severe AA ages 12 to 64 across 248 sites worldwide. More information on this trial can be found at www.clinicaltrials.gov (NCT06012240).
About RINVOQ® (upadacitinib)
Discovered and developed by AbbVie scientists, RINVOQ is a JAK inhibitor that is being studied in several immune-mediated inflammatory diseases. Based on enzymatic and cellular assays, RINVOQ demonstrated greater inhibitory potency for JAK-1 vs JAK-2, JAK-3, and TYK-2. The relevance of inhibition of specific JAK enzymes to therapeutic effectiveness and safety is not currently known.
Upadacitinib (RINVOQ) is being studied in Phase 3 clinical trials for alopecia areata, hidradenitis suppurativa, Takayasu arteritis, systemic lupus erythematosus, and vitiligo. The use of upadacitinib in alopecia areata is not approved; its safety and efficacy are under regulatory review by the U.S. FDA and the European Medicines Agency.
EU Indications and Important Safety Information about RINVOQ® (upadacitinib)7
Indications
Rheumatoid arthritis
RINVOQ is indicated for the treatment of moderate to severe active rheumatoid arthritis (RA) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (DMARDs). RINVOQ may be used as monotherapy or in combination with methotrexate.
Psoriatic arthritis
RINVOQ is indicated for the treatment of active psoriatic arthritis (PsA) in adult patients who have responded inadequately to, or who are intolerant to one or more DMARDs. RINVOQ may be used as monotherapy or in combination with methotrexate.
RINVOQ is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI), who have responded inadequately to nonsteroidal anti-inflammatory drugs (NSAIDs).
RINVOQ is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy.
Giant cell arteritis
RINVOQ is indicated for the treatment of giant cell arteritis (GCA) in adult patients.
Atopic dermatitis
RINVOQ is indicated for the treatment of moderate to severe atopic dermatitis (AD) in adults and adolescents 12 years and older who are candidates for systemic therapy.
Ulcerative colitis
RINVOQ is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.
Crohn's disease
RINVOQ is indicated for the treatment of adult patients with moderately to severely active Crohn's disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.
Important Safety Information
Contraindications
RINVOQ is contraindicated in patients hypersensitive to the active substance or to any of the excipients, in patients with active tuberculosis (TB) or active serious infections, in patients with severe hepatic impairment, and during pregnancy.
Special warnings and precautions for use
RINVOQ should only be used if no suitable treatment alternatives are available in patients:
65 years of age and older; patients with history of atherosclerotic cardiovascular (CV) disease or other CV risk factors (such as current or past long-time smokers); patients with malignancy risk factors (e.g. current malignancy or history of malignancy) Use in patients 65 years of age and older
Considering the increased risk of MACE, malignancies, serious infections, and all-cause mortality in patients ≥65 years of age, as observed in a large randomised study of tofacitinib (another Janus Kinase (JAK) inhibitor), RINVOQ should only be used in these patients if no suitable treatment alternatives are available. In patients ≥65 years of age, there is an increased risk of adverse reactions with RINVOQ 30 mg once daily. Consequently, the recommended dose for long-term use in this patient population is 15 mg once daily.
Immunosuppressive medicinal products
Use in combination with other potent immunosuppressants is not recommended.
Serious infections
Serious and sometimes fatal infections have been reported in patients receiving RINVOQ. The most frequent serious infections reported included pneumonia and cellulitis. Cases of bacterial meningitis and sepsis have been reported with RINVOQ. Among opportunistic infections, TB, multidermatomal herpes zoster, oral/esophageal candidiasis, and cryptococcosis have been reported. RINVOQ should not be initiated in patients with an active, serious infection, including localized infections. RINVOQ should be interrupted if a patient develops a serious or opportunistic infection until the infection is controlled. A higher rate of serious infections was observed with RINVOQ 30 mg compared to 15 mg. As there is a higher incidence of infections in the elderly and patients with diabetes in general, caution should be used when treating these populations. In patients ≥65 years of age, RINVOQ should only be used if no suitable treatment alternatives are available.
Tuberculosis
Patients should be screened for TB before starting RINVOQ. RINVOQ should not be given to patients with active TB. Anti-TB therapy may be appropriate for select patients in consultation with a physician with expertise in the treatment of TB. Patients should be monitored for the development of signs and symptoms of TB.
Viral reactivation
Viral reactivation, including cases of herpes zoster, was reported in clinical studies. The risk of herpes zoster appears to be higher in Japanese patients treated with RINVOQ. Consider interruption of RINVOQ if the patient develops herpes zoster until the episode resolves. Screening for viral hepatitis and monitoring for reactivation should occur before and during therapy. If hepatitis B virus DNA is detected, a liver specialist should be consulted.
Vaccination
The use of live, attenuated vaccines during or immediately prior to therapy is not recommended. It is recommended that patients be brought up to date with all immunizations, including prophylactic zoster vaccinations, prior to initiating RINVOQ, in agreement with current immunization guidelines.
Malignancy
Lymphoma and other malignancies have been reported in patients receiving JAK inhibitors, including RINVOQ. In a large randomised active‑controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a higher rate of malignancies, particularly lung cancer, lymphoma, and non-melanoma skin cancer (NMSC), was observed with tofacitinib compared to tumour necrosis factor (TNF) inhibitors. A higher rate of malignancies, including NMSC, was observed with RINVOQ 30 mg compared to 15 mg. Periodic skin examination is recommended for all patients, particularly those with risk factors for skin cancer. In patients ≥65 years of age, patients who are current or past long-time smokers, or patients with other malignancy risk factors (e.g., current malignancy or history of malignancy), RINVOQ should only be used if no suitable treatment alternatives are available.
Hematological abnormalities
Treatment should not be initiated, or should be temporarily interrupted, in patients with hematological abnormalities observed during routine patient management.
Gastrointestinal perforations
Events of diverticulitis and gastrointestinal perforations have been reported in clinical trials and from post-marketing sources. RINVOQ should be used with caution in patients who may be at risk for gastrointestinal perforation (e.g., patients with diverticular disease, a history of diverticulitis, or who are taking non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, or opioids. Patients with active Crohn's disease are at increased risk for developing intestinal perforation. Patients presenting with new onset abdominal signs and symptoms should be evaluated promptly for early identification of diverticulitis or gastrointestinal perforation.
Major adverse cardiovascular events
MACE were observed in clinical studies of RINVOQ. In a large randomised active-controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a higher rate of MACE, defined as CV death, non-fatal myocardial infarction and non-fatal stroke, was observed with tofacitinib compared to TNF inhibitors. Therefore, in patients ≥65 years of age, patients who are current or past long-time smokers, and patients with history of atherosclerotic CV disease or other CV risk factors, RINVOQ should only be used if no suitable treatment alternatives are available.
Lipids
RINVOQ treatment was associated with dose-dependent increases in lipid parameters, including total cholesterol, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol.
Hepatic transaminase elevations
Treatment with RINVOQ was associated with an increased incidence of liver enzyme elevation. Hepatic transaminases must be evaluated at baseline and thereafter according to routine patient management. If alanine transaminase (ALT) or aspartate transaminase (AST) increases are observed and drug-induced liver injury is suspected, RINVOQ should be interrupted until this diagnosis is excluded.
Venous thromboembolism
Events of deep venous thrombosis (DVT) and pulmonary embolism (PE) were observed in clinical trials for RINVOQ. In a large randomised active-controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a dose‑dependent higher rate of VTE including DVT and PE was observed with tofacitinib compared to TNF inhibitors. In patients with CV or malignancy risk factors, RINVOQ should only be used if no suitable treatment alternatives are available. In patients with known VTE risk factors other than CV or malignancy risk factors (e.g. previous VTE, patients undergoing major surgery, immobilisation, use of combined hormonal contraceptives or hormone replacement therapy, and inherited coagulation disorder), RINVOQ should be used with caution. Patients should be re-evaluated periodically to assess for changes in VTE risk. Promptly evaluate patients with signs and symptoms of VTE and discontinue RINVOQ in patients with suspected VTE.
Retinal vein occlusion
Retinal vein occlusion has been reported in patients treated with JAK inhibitors, including upadacitinib. Patients should be advised to promptly seek medical care in case they experience symptoms suggestive of retinal vein occlusion.
Hypersensitivity reactions
Serious hypersensitivity reactions such as anaphylaxis and angioedema have been reported in patients receiving RINVOQ. If a clinically significant hypersensitivity reaction occurs, discontinue RINVOQ and institute appropriate therapy.
Hypoglycemia in patients treated for diabetes
There have been reports of hypoglycemia following initiation of JAK inhibitors, including RINVOQ, in patients receiving medication for diabetes. Dose adjustment of anti-diabetic medication may be necessary in the event that hypoglycemia occurs.
Medication Residue in Stool
Reports of medication residue in stool or ostomy output have occurred in patients taking RINVOQ. Most reports described anatomic (e.g., ileostomy, colostomy, intestinal resection) or functional gastrointestinal conditions with shortened gastrointestinal transit times. Patients should be instructed to contact their healthcare professional if medication residue is observed repeatedly. Patients should be clinically monitored, and alternative treatment should be considered if there is an inadequate therapeutic response.
Giant Cell Arteritis
RINVOQ monotherapy should not be used for the treatment of acute relapses as efficacy in this setting has not been established. Corticosteroids should be given according to medical judgement and practice guidelines.
Adverse reactions
The most commonly reported adverse reactions in RA, PsA, and axSpA clinical trials (≥2% of patients in at least one of the indications) with RINVOQ 15 mg were upper respiratory tract infections, blood creatine phosphokinase (CPK) increased, ALT increased, bronchitis, nausea, neutropenia, cough, AST increased, and hypercholesterolemia. Overall, the safety profile observed in patients with psoriatic arthritis or active axial spondyloarthritis treated with RINVOQ 15 mg was consistent with the safety profile observed in patients with RA.
The most commonly reported adverse reactions in AD trials (≥2% of patients) with RINVOQ 15 mg or 30 mg were upper respiratory tract infection, acne, herpes simplex, headache, blood CPK increased, cough, folliculitis, abdominal pain, nausea, neutropenia, pyrexia, and influenza. Dose dependent increased risks of infection and herpes zoster were observed with RINVOQ. The safety profile for RINVOQ 15 mg and 30 mg in adolescents was similar to that in adults. With long-term exposure, skin papilloma was reported in adolescents in the RINVOQ 15 mg and 30 mg groups.
The most commonly reported adverse reactions in the UC and CD trials (≥3% of patients) with RINVOQ 45 mg, 30 mg or 15 mg were upper respiratory tract infection, pyrexia, blood CPK increased, anemia, headache, acne, herpes zoster, neutropenia, rash, pneumonia, hypercholesterolemia, bronchitis, AST increased, fatigue, folliculitis, ALT increased, herpes simplex, and influenza. The overall safety profile observed in patients with UC was generally consistent with that observed in patients with RA. Overall, the safety profile observed in patients with CD treated with RINVOQ was consistent with the known safety profile for RINVOQ.
Overall, the safety profile observed in patients with GCA treated with RINVOQ 15 mg was generally consistent with the known safety profile for RINVOQ.
The most common serious adverse reactions were serious infections.
The safety profile of RINVOQ with long-term treatment was generally similar to the safety profile during the placebo-controlled period across indications.
This is not a complete summary of all safety information.
See RINVOQ full Summary of Product Characteristics (SmPC) at www.ema.europa.eu.
Globally, prescribing information varies; refer to the individual country product label for complete information.
About AbbVie in Immunology
AbbVie is relentless in our pursuit to redefine the standard of care for patients living with immune-mediated conditions, with the goal of helping them live a life free from the limitations of their disease. For more than 20 years, AbbVie has led and helped shape the field of immunology through groundbreaking science and trusted medicines. Building on deep expertise across gastroenterology, rheumatology and dermatology, and other areas of high unmet need, we continue to invest in a broad and differentiated pipeline – spanning innovative modalities, novel mechanisms of actions and next-generation approaches designed to conquer the complex biology underlying immune-mediated disease.
Today, more than 1 million patients worldwide are treated with AbbVie's immunology medicines, approved in more than 175 countries across 19 immune-mediated diseases that impact adult and pediatric populations. As we work to strengthen our legacy and drive the next wave of innovation, we remain focused on delivering meaningful progress for patients and expanding access to our medicines. For more information, please visit www.abbvie.com/immunology.
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, neuroscience and oncology – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions and uses of future or conditional verbs, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements. Such risks and uncertainties include, but are not limited to, challenges to intellectual property, competition from other products, difficulties inherent in the research and development process, adverse litigation or government action, changes to laws and regulations applicable to our industry, the impact of global macroeconomic factors, such as economic downturns or uncertainty, international conflict, trade disputes and tariffs, and other uncertainties and risks associated with global business operations. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2025 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its Quarterly Reports on Form 10-Q and in other documents that AbbVie subsequently files with the Securities and Exchange Commission that update, supplement or supersede such information. AbbVie undertakes no obligation, and specifically declines, to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.
References
AbbVie. Data on file ABVRRTI81580. AbbVie. Data on file ABVRRTI81456. Alkhalifah A, Alsantali A, Wang E, McElwee KJ, Shapiro J. Alopecia areata update: Part I. Clinical picture, histopathology, and pathogenesis. J Am Acad Dermatol. 2010;62(2):177-188, quiz 189-190. Pratt CH, King LE, Messenger AG, Christiano AM, Sundberg JP. Alopecia areata. Nat Rev Dis Primers. 2017;3(1):17011 Davey L, Clarke V, Jenkinson E. Living with alopecia areata: an online qualitative survey study. Br J Dermatol. 2019;180(6):1377-1389 Bain KA, McDonald E, Moffat F, et al. Alopecia areata is characterized by dysregulation in systemic type 17 and type 2 cytokines, which may contribute to disease-associated psychological morbidity. Br J Dermatol. 2020;182(1):130-137 RINVOQ [Package Insert]. North Chicago, IL: AbbVie Inc.; 2026 SOURCE AbbVie
Broadcom vykázal rekordní výnosy 22,2 miliardy USD a výnosy z AI čipů vyskočily o 143 % na 10,8 miliardy USD. Akcie ale spadly, protože výhled v oblasti AI na další čtvrtletí zklamal.
Broadcom stock NASDAQ:AVGO has fallen sharply from its record high, but the selloff may say more about investor expectations than about weakness in AI demand.
Shares have retreated from around $495 to much lower levels, leaving the stock more than 24% below its peak.
That looks brutal, but Broadcom’s latest quarter was not a demand collapse. The company reported record revenue, strong earnings and a huge jump in AI semiconductor sales.
Broadcom’s fiscal second-quarter numbers were strong on the surface.
Revenue rose 48% from a year earlier to a record $22.2 billion, while adjusted earnings came in at $2.44 a share. AI semiconductor revenue jumped 143% year on year to $10.8 billion.
The real trigger was guidance. Broadcom said it expects AI chip revenue of about $16 billion in the fiscal third quarter.
That would still be more than triple the year-earlier level, but it came in below the roughly $17 billion-plus investors had hoped for.
The bigger disappointment was that CEO Hock Tan did not raise Broadcom’s longer-term AI target. He reiterated that the company is still aiming for more than $100 billion in AI chip sales in fiscal 2027.
In this market, “on track” was not enough.
Trading volume surged as the stock fell, showing this was a panic-style reset rather than a slow reassessment.
Broadcom’s management still sounds confident about demand.
Tan said demand for XPUs and networking is “simply insatiable,” adding that AI semiconductor bookings in the quarter were over $30 billion against the $10.8 billion the company shipped.
That means customers are still ordering far more than Broadcom can currently deliver.
The company has also pointed to gigawatt-scale commitments from major AI customers, including Anthropic, OpenAI and Meta.
Broadcom now expects to ship more than 10 gigawatts of AI chips in 2027, slightly above its earlier view.
Wall Street has not abandoned the stock either. JPMorgan reiterated its Overweight rating and $580 price target, telling clients it would be “aggressive buyers” at current levels.
The broader analyst picture remains heavily bullish. Recent consensus screens show dozens of Buy ratings, only a handful of Holds and no Sells, with average price targets still above $500.
There are real risks as CFO Kirsten Spears has previously flagged margin pressure as AI becomes a bigger part of Broadcom’s mix, because some AI system sales may carry lower margins than its software business.
Tan has also acknowledged that Google may diversify TPU suppliers over time, even though Broadcom remains central to Google’s custom chip roadmap.
Broadcom’s drop did not happen in isolation.
The selloff spilled into the broader semiconductor space, with Nvidia, AMD, Marvell, Intel, Micron and other chip names also coming under pressure in the days after the report.
Texas Instruments and Analog Devices were hit in a wider chip-sector pullback as investors questioned whether AI-related valuations had run too far.
The market was looking for any sign that the AI trade had become too crowded.
Broadcom’s decision not to raise its long-term target gave investors an excuse to take profits across the group.
Helen of Troy Limited (NASDAQ:HELE) will release earnings for its first quarter before the opening bell on Wednesday, July 8.
Analysts expect the El Paso, Texas-based company to report quarterly earnings of 1 cent per share, down from 41 cents per share in the year-ago period. The consensus estimate for Helen of Troy’s quarterly revenue is $374.55 million. It reported $371.65 million last year, according to Benzinga Pro.
On April 23, Helen of Troy reported better-than-expected fourth-quarter financial results and issued FY27 GAAP EPS guidance above estimates.
Shares of Helen of Troy rose 2% to close at $28.38 on Friday.
Benzinga readers can access the latest analyst ratings on the Analyst Stock Ratings page. Readers can sort by stock ticker, company name, analyst firm, rating change or other variables.
Let’s have a look at how Benzinga’s most-accurate analysts have rated the company in the recent period.
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BT Group a Verizon vytvoří společný podnik v poměru 50:50 pro mezinárodní konektivitu. Nový podnik má obsluhovat více než 3 000 zákazníků ve více než 180 zemích s kombinovanými ročními tržbami kolem 4 miliard USD.
June 29, 2026 02:00 ET | Source: Verizon Communications, Inc.
BT Group and Verizon agree to combine their respective international operations in a 50:50 joint venture, creating a new company focused on multinational connectivity.The joint venture will serve more than 3,000 customers across more than 180 countries, representing approx. $4 billion in combined annual revenue.The combination of international networking businesses creates a future-ready, scaled organization underpinned by a new platform designed for the age of cloud and AI.Martijn Blanken is appointed Chief Executive Officer-designate of the new joint venture, conditional on completion of the transaction.The transaction is expected to complete in 2027, subject to regulatory clearances and other customary closing conditions. LONDON and NEW YORK, June 29, 2026 (GLOBE NEWSWIRE) -- BT Group (BT) and Verizon Communications Inc. (NYSE, Nasdaq: VZ) today announced the signing of an agreement to combine their respective international enterprise operations into a 50:50 joint venture – in a move that is set to transform international connectivity.
The new joint venture will focus on serving multinational organizations. It is expected to serve more than 3,000 customers across more than 180 countries, representing approximately $4 billion in combined annual revenue. This breadth of operations will unlock significant scale efficiencies across the combined global network and service operations following completion.
Designed specifically for a cloud-first world in the age of AI, the joint venture brings together BT International, which serves multinational customers with secure and resilient communication and network services around the world, with Verizon’s international enterprise wireline arm, which provides secure connectivity to enterprises worldwide. Both BT and Verizon will hold equal voting rights and Verizon has agreed to pay BT an equalization payment of $625 million.
By combining global scale with infrastructure designed and built to support local compliance and sovereignty needs, the joint venture will create a stronger platform for growth and accelerate the rollout of next-generation connectivity platforms. Customers will benefit from secure and resilient connectivity designed to meet data, operational and regulatory requirements.
At the same time, the parent companies will be better able to focus on their domestic markets, while providing support to the new joint venture as equal shareholders.
BT and Verizon have also today confirmed that Martijn Blanken has been appointed Chief Executive Officer-designate of the new joint venture, conditional on the completion of the transaction. Martijn has almost three decades in senior leadership positions across telecommunications, technology and digital infrastructure at Telstra, Openwave Systems, EXA Infrastructure and KPN, and a career spanning four continents. From September 1, 2026, he will join BT and will work with both parent companies, while observing relevant regulatory requirements, as they prepare for the launch of the proposed joint venture.
Clive Selley will continue to lead BT International as CEO, ensuring continuity of BT International’s ongoing transformation in readiness for the creation of the joint venture. Verizon’s leadership remains unchanged.
Allison Kirkby, Chief Executive of BT Group, said: “The world’s leading brands and international organizations trust BT International to connect them across the world. Bringing together this expertise and heritage with Verizon’s deep relationships with multinationals will create a stronger, scaled connectivity partner – one that has the reach, innovation and investment to succeed. Customers will benefit from new, secure and resilient connectivity platforms which are designed for the age of AI and sovereign where it matters. It will create new opportunities for our people and long-term value for our owners. Today’s announcement marks a major milestone for BT International, and an important step forward for BT as a whole, as we deliver on our U.K.-focused strategy.”
Dan Schulman, CEO of Verizon, said: "Our international customers require secure, flexible connectivity that works seamlessly across borders and cloud environments. When we thought about how to best support them, this joint venture was the clear answer: a cutting-edge, AI-ready and secure platform run by a single global organization dedicated to their needs. At the same time, our relationship with those customers will stay equally strong as we continue to directly provide them with the connectivity they need in the U.S."
The transaction is subject to regulatory clearances and consultation with employee representations in countries where required. BT and Verizon’s international businesses will continue to operate independently until the transaction officially closes with a full commitment to their respective customers.
Additional information
The new joint venture will be incorporated in the Bailiwick of Jersey and headquartered and tax resident in the United Kingdom.On completion of the transaction, the new joint venture will establish commercial relationships with both BT and Verizon – providing a seamless, end-to-end service across borders including for our customers in the U.K. (BT) and the U.S. (Verizon).Goldman Sachs acted as lead financial advisor to BT, with Deloitte transaction services advisor and Freshfields LLP as legal counsel. Morgan Stanley & Co. LLC acted as financial advisors to Verizon and Kirkland & Ellis LLP acted as legal counsel. Verizon Forward-Looking Statements
This communication contains forward-looking statements. These statements are based on our estimates and assumptions and are subject to risks and uncertainties. Forward-looking statements include those regarding our possible or assumed future results of operations and those regarding our ability to consummate the proposed transaction with BT Group plc and obtain cost savings, synergies and other anticipated benefits within the expected time period or at all. Forward-looking statements also include those preceded or followed by the words "anticipates," "assumes," "believes," "estimates," "expects," "forecasts," "hopes," "intends," "plans," "targets," “will” or similar expressions. For those statements, we claim the protection of the safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. We undertake no obligation to revise or publicly release the results of any revision to these forward-looking statements, except as required by law. Given these risks and uncertainties, readers are cautioned not to place undue reliance on such forward-looking statements.
This announcement was originally published by Verizon. Read the original press release.
About BT Group
BT Group is the U.K.’s leading provider of fixed and mobile telecommunications and related secure digital products, solutions and services.
BT Group consists of four customer-facing units: Consumer serves individuals and families in the U.K.; Business covers companies and public services in the U.K.; International serves multinational organisations headquartered outside the U.K. and overseas public sector customers; Openreach is an independently governed, wholly owned subsidiary wholesaling fixed access infrastructure services to its customers – over 700 communications providers across the U.K.
British Telecommunications Limited is a wholly owned subsidiary of BT Group plc and encompasses virtually all businesses and assets of the BT Group. BT Group plc is listed on the London Stock Exchange.
For more information, visit www.bt.com/about
About Verizon
Verizon Communications Inc. (NYSE, Nasdaq: VZ) powers and empowers how its millions of customers live, work and play, delivering on their demand for mobility, reliable network connectivity and security. Headquartered in New York City, serving countries worldwide and nearly all of the Fortune 500, Verizon generated revenues of $138.2 billion in 2025. Verizon’s world-class team never stops innovating to meet customers where they are today and equip them for the needs of tomorrow. For more, visit verizon.com or find a retail location at verizon.com/stores
VERIZON’S ONLINE MEDIA CENTER: News releases, stories, media contacts and other resources are available at verizon.com/news. News releases are also available through an RSS feed. To subscribe, visit www.verizon.com/about/rss-feeds/.
Media contacts:
Sarah Heinz (Verizon) [email protected]
347-931-6300
GLP-1 léky Pfizeru a Innoventu prošly v Číně předběžným posouzením pro možné zařazení do základního seznamu zdravotního pojištění. Akcie Innoventu po oznámení vzrostly asi o 7 %.
A logo of Pfizer at the company’s booth at the 8th China International Import Expo (CIIE) in Shanghai, China, November 6, 2025.REUTERS/Maxim Shemetov/File Photo Purchase Licensing Rights, opens new tab
CompaniesSHANGHAI, June 29 (Reuters) - GLP-1 drugs from Pfizer (PFE.N), opens new tab and Innovent Biologics (1801.HK), opens new tab have passed a preliminary review to be potentially included in China's basic medical insurance drug catalogue, a list published by the National Healthcare Security Administration showed on Monday.
Pfizer's ecnoglutide and Innovent's mazdutide, approved in China as treatments for weight management and type II diabetes, belong to the class of GLP-1 receptor agonist drugs already included in China's state insurance list from drugmakers such as Novo Nordisk (NOVOb.CO), opens new tab, Eli Lilly (LLY.N), opens new tab and Guangzhou Innogen Pharmaceutical Group (2591.HK), opens new tab.
Keep up with the latest medical breakthroughs and healthcare trends with the Reuters Health Rounds newsletter. Sign up here.
Innovent shares were up about 7% after the announcement.
Novo's Ozempic was first added to China's reimbursement list in 2022, followed by Lilly's Mounjaro and Innogen's efsubaglutide alfa from this year for patients with type II diabetes. Inclusion in the national reimbursement list makes drugs more widely available to the public in a country with a population of 1.4 billion, though an increase in sales volume is often mitigated by lower prices.
Sales of Ozempic injector pens in mainland China, Taiwan and Hong Kong — Novo's largest market after the U.S. — slipped 7% to about 5.4 billion Danish crowns ($853 million) in 2025.
Sales of GLP-1 treatments in China through major e-commerce platforms Alibaba (9988.HK), opens new tab and JD.com (9618.HK), opens new tab totalled about 1.4 billion yuan ($207 million) in the first quarter of 2026, according to Jefferies.
A spokesperson for Pfizer did not immediately respond to a request for comment.
A spokesperson for Innovent told Reuters that in terms of medical insurance coverage in China only treatment for diabetes could be considered.
Reporting by Andrew Silver; Additional reporting by Ethan Wang and Ryan Woo; Editing by Tom Hogue and Muralikumar Anantharaman
Our Standards: The Thomson Reuters Trust Principles., opens new tab
AbbVie získala kladné stanovisko CHMP k registraci upadacitinibu pro léčbu dospělých a dospívajících s nesegmentálním vitiligem. Pokud bude schválen, měl by být první systémovou léčbou pro toto onemocnění.
If approved, upadacitinib is expected to be the first systemic medication for patients with non-segmental vitiligo, addressing important treatment needs for those living with the chronic, unpredictable autoimmune disease Positive CHMP opinion is supported by data from the Phase 3 Viti-Up clinical studies, in which upadacitinib achieved both co-primary endpoints demonstrating at least a 50% improvement in total body repigmentation (T-VASI 50) and at least a 75% improvement in facial repigmentation (F-VASI 75) from baseline at week 481 , /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending the approval of upadacitinib (RINVOQ®; 15 mg, once daily) for the treatment of adult and adolescent patients with non-segmental vitiligo (NSV). The final European Commission decision is expected in the coming months. If approved, upadacitinib is expected to be the first systemic medication for patients with non-segmental vitiligo.
"Vitiligo is an autoimmune skin disease with high stigma and significant burden to patients with limited treatment options available," said Roopal Thakkar, M.D., executive vice president, research and development, chief scientific officer, AbbVie. "A positive opinion for upadacitinib in non-segmental vitiligo is an important step forward in providing patients with a systemic treatment option."
The CHMP positive opinion is supported by data from the ongoing Phase 3 Viti-Up clinical program, including two replicate, randomized, placebo-controlled, double-blind studies evaluating the efficacy and safety of upadacitinib in adult and adolescent patients with NSV. Upadacitinib 15 mg met both co-primary endpoints and key secondary endpoints, with significant improvements in total body and facial repigmentation.1 The safety profile of upadacitinib 15 mg was consistent with that observed in approved indications, with no new safety signals.1
Upadacitinib is approved in the European Union (EU) for the treatment of adults and adolescents with atopic dermatitis, and adults with radiographic axial spondylarthritis, non-radiographic axial spondylarthritis, psoriatic arthritis, rheumatoid arthritis, ulcerative colitis, Crohn's disease, and giant cell arteritis. Use of upadacitinib in NSV is not currently approved in the EU.
About Vitiligo
Vitiligo is a chronic, autoimmune disease characterized by the loss of pigment-producing cells (melanocytes), resulting in white patches of skin that can appear anywhere on the body and at any time.2 It imposes a significant psychosocial burden, profoundly affecting an individual's confidence, identity and daily life.3 Non-segmental vitiligo (NSV), the most common form of vitiligo afflicting approximately 84% of patients, is marked by symmetrical and bilateral depigmented white patches and is prone to unpredictable progression even after long periods of stability.2,4-6 While location varies, many patients report patches on critical areas such as the face, feet, hands and groin. Despite its immune-mediated nature, vitiligo is often considered primarily a cosmetic problem, which can lead to stigma and psychological impact on patients' lives.7-9 Vitiligo management is anchored in three primary treatment goals: disease stabilization, repigmentation, and maintaining repigmentation.10,11 There are currently no approved systemic medicines specifically indicated for these treatment goals in vitiligo.
About Viti-Up Clinical Trials
Upadacitinib M19-044 was conducted under a single protocol encompassing two replicate Phase 3 studies (Study 1 and Study 2) with independent randomization, investigative sites, data collection, analysis and reporting for each study. The trials were designed to evaluate the efficacy, safety and tolerability of upadacitinib in adult and adolescent patients (ages 12 and older) living with non-segmental vitiligo (NSV) who were eligible for systemic therapy. In Period A of both studies, participants were randomized in a 2:1 ratio to receive either upadacitinib 15 mg once daily or placebo for 48 weeks. Participants who completed Period A were eligible to enter Period B, a 112-week open-label extension in which all patients received upadacitinib 15 mg once daily. In total, Study 1 and Study 2 Periods A and B span 160 weeks. The two trials randomized 614 participants with NSV across 90 sites worldwide. More information on these trials can be found at www.clinicaltrials.gov (NCT06118411).
The co-primary endpoints were based on the achievement of Total Vitiligo Area Scoring Index (T-VASI) 50, defined as at least 50% reduction in T-VASI from baseline, at week 48, and the achievement of Facial Vitiligo Area Scoring Index (F-VASI) 75, defined as at least 75% reduction in F-VASI from baseline, at week 48 with the treatment of upadacitinib 15 mg compared with placebo in adults and adolescents with NSV.
The secondary endpoints include the achievement of F-VASI 50, defined as at least a 50% reduction in F-VASI from baseline, at week 48, and the achievement of F-VASI 75, defined as at least a 75% reduction in facial vitiligo area from baseline, at week 24. These endpoints were designed to assess the degree and timing of re-pigmentation on the face, an area among the most visible and psychosocially impactful for people living with NSV.
About RINVOQ® (upadacitinib)
Discovered and developed by AbbVie scientists, RINVOQ is a JAK inhibitor that is being studied in several immune-mediated inflammatory diseases. Based on enzymatic and cellular assays, RINVOQ demonstrated greater inhibitory potency for JAK-1 vs JAK-2, JAK-3, and TYK-2. The relevance of inhibition of specific JAK enzymes to therapeutic effectiveness and safety is not currently known.
Upadacitinib (RINVOQ) is being studied in Phase 3 clinical trials for alopecia areata, hidradenitis suppurativa, Takayasu arteritis, systemic lupus erythematosus, and vitiligo. The use of upadacitinib in non-segmental vitiligo is not approved; its safety and efficacy are under regulatory review by the U.S. FDA and the European Medicines Agency.
EU Indications and Important Safety Information about RINVOQ® (upadacitinib)12
Indications
Rheumatoid arthritis
RINVOQ is indicated for the treatment of moderate to severe active rheumatoid arthritis (RA) in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (DMARDs). RINVOQ may be used as monotherapy or in combination with methotrexate.
Psoriatic arthritis
RINVOQ is indicated for the treatment of active psoriatic arthritis (PsA) in adult patients who have responded inadequately to, or who are intolerant to one or more DMARDs. RINVOQ may be used as monotherapy or in combination with methotrexate.
RINVOQ is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated C-reactive protein (CRP) and/or magnetic resonance imaging (MRI), who have responded inadequately to nonsteroidal anti-inflammatory drugs (NSAIDs).
RINVOQ is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy.
Giant cell arteritis
RINVOQ is indicated for the treatment of giant cell arteritis (GCA) in adult patients.
Atopic dermatitis
RINVOQ is indicated for the treatment of moderate to severe atopic dermatitis (AD) in adults and adolescents 12 years and older who are candidates for systemic therapy.
Ulcerative colitis
RINVOQ is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.
Crohn's disease
RINVOQ is indicated for the treatment of adult patients with moderately to severely active Crohn's disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.
Important Safety Information
Contraindications
RINVOQ is contraindicated in patients hypersensitive to the active substance or to any of the excipients, in patients with active tuberculosis (TB) or active serious infections, in patients with severe hepatic impairment, and during pregnancy.
Special warnings and precautions for use
RINVOQ should only be used if no suitable treatment alternatives are available in patients:
- 65 years of age and older;
- patients with history of atherosclerotic cardiovascular (CV) disease or other CV risk factors (such as current or past long-time smokers);
- patients with malignancy risk factors (e.g. current malignancy or history of malignancy)
Use in patients 65 years of age and older
Considering the increased risk of MACE, malignancies, serious infections, and all-cause mortality in patients ≥65 years of age, as observed in a large randomised study of tofacitinib (another Janus Kinase (JAK) inhibitor), RINVOQ should only be used in these patients if no suitable treatment alternatives are available. In patients ≥65 years of age, there is an increased risk of adverse reactions with RINVOQ 30 mg once daily. Consequently, the recommended dose for long-term use in this patient population is 15 mg once daily.
Immunosuppressive medicinal products
Use in combination with other potent immunosuppressants is not recommended.
Serious infections
Serious and sometimes fatal infections have been reported in patients receiving RINVOQ. The most frequent serious infections reported included pneumonia and cellulitis. Cases of bacterial meningitis and sepsis have been reported with RINVOQ. Among opportunistic infections, TB, multidermatomal herpes zoster, oral/esophageal candidiasis, and cryptococcosis have been reported. RINVOQ should not be initiated in patients with an active, serious infection, including localized infections. RINVOQ should be interrupted if a patient develops a serious or opportunistic infection until the infection is controlled. A higher rate of serious infections was observed with RINVOQ 30 mg compared to 15 mg. As there is a higher incidence of infections in the elderly and patients with diabetes in general, caution should be used when treating these populations. In patients ≥65 years of age, RINVOQ should only be used if no suitable treatment alternatives are available.
Tuberculosis
Patients should be screened for TB before starting RINVOQ. RINVOQ should not be given to patients with active TB. Anti-TB therapy may be appropriate for select patients in consultation with a physician with expertise in the treatment of TB. Patients should be monitored for the development of signs and symptoms of TB.
Viral reactivation
Viral reactivation, including cases of herpes zoster, was reported in clinical studies. The risk of herpes zoster appears to be higher in Japanese patients treated with RINVOQ. Consider interruption of RINVOQ if the patient develops herpes zoster until the episode resolves. Screening for viral hepatitis and monitoring for reactivation should occur before and during therapy. If hepatitis B virus DNA is detected, a liver specialist should be consulted.
Vaccination
The use of live, attenuated vaccines during or immediately prior to therapy is not recommended. It is recommended that patients be brought up to date with all immunizations, including prophylactic zoster vaccinations, prior to initiating RINVOQ, in agreement with current immunization guidelines.
Malignancy
Lymphoma and other malignancies have been reported in patients receiving JAK inhibitors, including RINVOQ. In a large randomised active-controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a higher rate of malignancies, particularly lung cancer, lymphoma, and non-melanoma skin cancer (NMSC), was observed with tofacitinib compared to tumour necrosis factor (TNF) inhibitors. A higher rate of malignancies, including NMSC, was observed with RINVOQ 30 mg compared to 15 mg. Periodic skin examination is recommended for all patients, particularly those with risk factors for skin cancer. In patients ≥65 years of age, patients who are current or past long-time smokers, or patients with other malignancy risk factors (e.g., current malignancy or history of malignancy), RINVOQ should only be used if no suitable treatment alternatives are available.
Hematological abnormalities
Treatment should not be initiated, or should be temporarily interrupted, in patients with hematological abnormalities observed during routine patient management.
Gastrointestinal perforations
Events of diverticulitis and gastrointestinal perforations have been reported in clinical trials and from post-marketing sources. RINVOQ should be used with caution in patients who may be at risk for gastrointestinal perforation (e.g., patients with diverticular disease, a history of diverticulitis, or who are taking non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, or opioids. Patients with active Crohn's disease are at increased risk for developing intestinal perforation. Patients presenting with new onset abdominal signs and symptoms should be evaluated promptly for early identification of diverticulitis or gastrointestinal perforation.
Major adverse cardiovascular events
MACE were observed in clinical studies of RINVOQ. In a large randomised active-controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a higher rate of MACE, defined as CV death, non-fatal myocardial infarction and non-fatal stroke, was observed with tofacitinib compared to TNF inhibitors. Therefore, in patients ≥65 years of age, patients who are current or past long-time smokers, and patients with history of atherosclerotic CV disease or other CV risk factors, RINVOQ should only be used if no suitable treatment alternatives are available.
Lipids
RINVOQ treatment was associated with dose-dependent increases in lipid parameters, including total cholesterol, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol.
Hepatic transaminase elevations
Treatment with RINVOQ was associated with an increased incidence of liver enzyme elevation. Hepatic transaminases must be evaluated at baseline and thereafter according to routine patient management. If alanine transaminase (ALT) or aspartate transaminase (AST) increases are observed and drug-induced liver injury is suspected, RINVOQ should be interrupted until this diagnosis is excluded.
Venous thromboembolism
Events of deep venous thrombosis (DVT) and pulmonary embolism (PE) were observed in clinical trials for RINVOQ. In a large randomised active-controlled study of tofacitinib (another JAK inhibitor) in RA patients ≥50 years of age with ≥1 additional CV risk factor, a dose‑dependent higher rate of VTE including DVT and PE was observed with tofacitinib compared to TNF inhibitors. In patients with CV or malignancy risk factors, RINVOQ should only be used if no suitable treatment alternatives are available. In patients with known VTE risk factors other than CV or malignancy risk factors (e.g. previous VTE, patients undergoing major surgery, immobilisation, use of combined hormonal contraceptives or hormone replacement therapy, and inherited coagulation disorder), RINVOQ should be used with caution. Patients should be re-evaluated periodically to assess for changes in VTE risk. Promptly evaluate patients with signs and symptoms of VTE and discontinue RINVOQ in patients with suspected VTE.
Retinal vein occlusion
Retinal vein occlusion has been reported in patients treated with JAK inhibitors, including upadacitinib. Patients should be advised to promptly seek medical care in case they experience symptoms suggestive of retinal vein occlusion.
Hypersensitivity reactions
Serious hypersensitivity reactions such as anaphylaxis and angioedema have been reported in patients receiving RINVOQ. If a clinically significant hypersensitivity reaction occurs, discontinue RINVOQ and institute appropriate therapy.
Hypoglycemia in patients treated for diabetes
There have been reports of hypoglycemia following initiation of JAK inhibitors, including RINVOQ, in patients receiving medication for diabetes. Dose adjustment of anti-diabetic medication may be necessary in the event that hypoglycemia occurs.
Medication Residue in Stool
Reports of medication residue in stool or ostomy output have occurred in patients taking RINVOQ. Most reports described anatomic (e.g., ileostomy, colostomy, intestinal resection) or functional gastrointestinal conditions with shortened gastrointestinal transit times. Patients should be instructed to contact their healthcare professional if medication residue is observed repeatedly. Patients should be clinically monitored, and alternative treatment should be considered if there is an inadequate therapeutic response.
Giant Cell Arteritis
RINVOQ monotherapy should not be used for the treatment of acute relapses as efficacy in this setting has not been established. Corticosteroids should be given according to medical judgement and practice guidelines.
Adverse reactions
The most commonly reported adverse reactions in RA, PsA, and axSpA clinical trials (≥2% of patients in at least one of the indications) with RINVOQ 15 mg were upper respiratory tract infections, blood creatine phosphokinase (CPK) increased, ALT increased, bronchitis, nausea, neutropenia, cough, AST increased, and hypercholesterolemia. Overall, the safety profile observed in patients with psoriatic arthritis or active axial spondyloarthritis treated with RINVOQ 15 mg was consistent with the safety profile observed in patients with RA.
The most commonly reported adverse reactions in AD trials (≥2% of patients) with RINVOQ 15 mg or 30 mg were upper respiratory tract infection, acne, herpes simplex, headache, blood CPK increased, cough, folliculitis, abdominal pain, nausea, neutropenia, pyrexia, and influenza. Dose dependent increased risks of infection and herpes zoster were observed with RINVOQ. The safety profile for RINVOQ 15 mg and 30 mg in adolescents was similar to that in adults. With long-term exposure, skin papilloma was reported in adolescents in the RINVOQ 15 mg and 30 mg groups.
The most commonly reported adverse reactions in the UC and CD trials (≥3% of patients) with RINVOQ 45 mg, 30 mg or 15 mg were upper respiratory tract infection, pyrexia, blood CPK increased, anemia, headache, acne, herpes zoster, neutropenia, rash, pneumonia, hypercholesterolemia, bronchitis, AST increased, fatigue, folliculitis, ALT increased, herpes simplex, and influenza. The overall safety profile observed in patients with UC was generally consistent with that observed in patients with RA. Overall, the safety profile observed in patients with CD treated with RINVOQ was consistent with the known safety profile for RINVOQ.
Overall, the safety profile observed in patients with GCA treated with RINVOQ 15 mg was generally consistent with the known safety profile for RINVOQ.
The most common serious adverse reactions were serious infections.
The safety profile of RINVOQ with long-term treatment was generally similar to the safety profile during the placebo-controlled period across indications.
This is not a complete summary of all safety information.
See RINVOQ full Summary of Product Characteristics (SmPC) at www.ema.europa.eu
Globally, prescribing information varies; refer to the individual country product label for complete information.
About AbbVie in Immunology
AbbVie is relentless in our pursuit to redefine the standard of care for patients living with immune-mediated conditions, with the goal of helping them live a life free from the limitations of their disease. For more than 20 years, AbbVie has led and helped shape the field of immunology through groundbreaking science and trusted medicines. Building on deep expertise across gastroenterology, rheumatology and dermatology, and other areas of high unmet need, we continue to invest in a broad and differentiated pipeline – spanning innovative modalities, novel mechanisms of actions and next-generation approaches designed to conquer the complex biology underlying immune-mediated disease.
Today, more than 1 million patients worldwide are treated with AbbVie's immunology medicines, approved in more than 175 countries across 19 immune-mediated diseases that impact adult and pediatric populations. As we work to strengthen our legacy and drive the next wave of innovation, we remain focused on delivering meaningful progress for patients and expanding access to our medicines. For more information, please visit www.abbvie.com/immunology.
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, neuroscience and oncology – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions and uses of future or conditional verbs, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements. Such risks and uncertainties include, but are not limited to, challenges to intellectual property, competition from other products, difficulties inherent in the research and development process, adverse litigation or government action, changes to laws and regulations applicable to our industry, the impact of global macroeconomic factors, such as economic downturns or uncertainty, international conflict, trade disputes and tariffs, and other uncertainties and risks associated with global business operations. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2025 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its Quarterly Reports on Form 10-Q and in other documents that AbbVie subsequently files with the Securities and Exchange Commission that update, supplement or supersede such information. AbbVie undertakes no obligation, and specifically declines, to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.
References
AbbVie. Data on file ABVRRTI82545 Ezzedine K, Eleftheriadou V, Whitton M, van Geel N. Vitiligo. Lancet. 2015;386(9988):74-84. doi:10.1016/S0140-6736(14)60763-7 Krüger C, Schallreuter KU. A review of the worldwide prevalence of vitiligo in children/adolescents and adults. Int J Dermatol. 2012;51(10):1206-1212. doi:10.1111/j.1365-4632.2011.05377.x Mazzei Weiss ME. Vitiligo: to biopsy or not to biopsy?. Cutis. 2020;105(4):189-190. Ezzedine K, Lim HW, Suzuki T, et al. Revised classification/nomenclature of vitiligo and related issues: the Vitiligo Global Issues Consensus Conference. Pigment Cell Melanoma Res. 2012;25(3):E1-13 Taneja N, Sreenivas V, Sahni K, Gupta V, Ramam M. Disease Stability in Segmental and Non-Segmental Vitiligo. Indian Dermatol Online J. 2021 Aug 2;13(1):60-63. doi: 10.4103/idoj.IDOJ_154_21. PMID: 35198469; PMCID: PMC8809159 Hlača N, Žagar T, Kaštelan M, Brajac l, Prpić-Massari L. Current concepts of vitiligo immunopathogenesis. Biomedicines. 2022;10(7):1639. doi:10.3390/biomedicines10071639 Abdel-Malek ZA, Jordan C, Ho T, Upadhyay PR, Fleischer A, Hamzavi l. The enigma and challenges of vitiligo pathophysiology and treatment. Pigment Cell Melanoma Res. 2020;33(6):778-787. doi:10.1111/pcmr.12878 Birlea SA, Goldstein NB, Norris DA. Repigmentation through melanocyte regeneration in vitiligo. Dermatol Clin. 2017;35(2):205-218. doi:10.1016/j.det.2016.11.015 van Geel N, Speeckaert R, Taïeb A, et al. Worldwide expert recommendations for the diagnosis and management of vitiligo: position statement from the International Vitiligo Task Force part 1: towards a new management algorithm. J Eur Acad Dermatol Venereol. 2023;37(11):2173-2184. doi:10.1111/jdv.19451 Seneschal J, Boniface K. Vitiligo: Current therapies and future treatments. Dermatol Pract Concept. 2023;13(4S2):e2023313S. doi:10.5826/dpc.1304S2a313 RINVOQ [Package Insert]. North Chicago, IL: AbbVie Inc.; 2026 SOURCE AbbVie
Toyota Motor's all-new RAV4 SUVs are displayed during its world premiere event in Tokyo, Japan May 21, 2025. REUTERS/Manami Yamada Purchase Licensing Rights, opens new tab
CompaniesTOKYO, June 29 (Reuters) - Toyota Motor (7203.T), opens new tab said on Monday that global vehicle sales slipped for a fourth consecutive month in May, as decreases in China and the Middle East weighed on overall results.
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Global sales dropped 7.2% year-on-year to 834,279 vehicles, Toyota said in a release. Overseas sales fell 9.6%, while those in Japan rose 11.1%, helped by strong demand for models such as RAV4 and bZ4X.
By region, sales in China plunged 31.7% amid tough market conditions, partly due to rising petrol prices, while those in the Middle East slumped 38.6%. In the U.S., Toyota's top market, they edged down 0.6%.
Global production declined 5.5% from a year earlier, as a 3.8% drop in the U.S. and a 13.3% decrease in Asia offset a rise in Japan.
Toyota's figures include its luxury brand, Lexus.
Reporting by Daniel Leussink; Editing by Rashmi Aich
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PUMP za den vzrostl o 12 % a počet držitelů dosáhl rekordu 122 440. Aktivita platformy ale slábne, když objem na launchpadu, poplatky i tržby dál klesají. Tržby protokolu klesly o 23 % na 147,8 milionu USD.
Sentiment around cryptocurrency memecoin launch platform Pump.fun [PUMP] has turned positive again following renewed interest in memecoins over the past day.
The platform’s native token moved alongside that momentum, with PUMP surging 12% over the past day.
Even so, the rally remained tied to the platform’s underlying health, leaving investors exposed if protocol activity failed to recover.
Why are investors buying PUMP? PUMP’s recent rally has coincided with growing investor participation. The token’s holder count reached a record 122,440, while retail investors accounted for roughly 38% of holders.
That increase also appeared in on-chain data, suggesting fresh capital supported the recent move.
Source: DeFiLlama Between the 26th of June and now, investors added roughly $15.7 million to Total Value Locked (TVL), lifting it to $217.7 million. Those inflows suggested investors committed more capital despite recent volatility.
Total Value Locked measures assets deposited into DeFi protocols. Rising TVL often reflects stronger long-term conviction while investors earn yield.
Is the protocol keeping up? However, rising TVL did not match the protocol’s underlying performance.
Pump.fun continued underperforming across key metrics, including revenue, fees, and launchpad volume.
Data from Artemis showed launchpad volume and fees generated by memecoins on the platform fell 86.7% and 35.6% to $5.8 million and $587,200, respectively.
Source: Artemis Those declines suggested user activity remained weak despite improving investor sentiment.
Lower activity reduced fee generation and limited protocol utility, making it harder for the recent price recovery to gain stronger fundamental support.
Revenue reflected the same trend.
Protocol revenue fell 23% to $147.8 million, reinforcing signs of slowing activity.
Historically, sustained token rallies have been easier to support when protocol usage improves alongside price. Until those metrics recover, PUMP’s recent optimism could remain vulnerable.
Final Summary PUMP gained 12%, holder count hit a record, and TVL increased sharply, signaling renewed market interest. If protocol metrics fail to recover, investor optimism may prove difficult to sustain.
Ambea podala doporučenou veřejnou nabídku na převzetí společnosti Humana, kterou oceňuje přibližně na 2,96 miliardy SEK. Akcionáři mají obdržet 20 SEK v hotovosti, 0,305 akcie Ambea a jedno podmíněné právo na akcii.
CompaniesJune 29 (Reuters) - Swedish care provider Ambea (AMBEA.ST), opens new tab said on Monday it had made a recommended public offer for peer Humana (HUMAN.ST), opens new tab, valuing the company at about 2.96 billion Swedish crowns ($304.13 million).
Ambea is offering Humana shareholders SEK 20 in cash, 0.305 Ambea shares and one contingent value right for each Humana share.
The cash-and-share part of the offer corresponds to SEK 62.30 per Humana share, a 26.8% premium to Humana's closing price on June 26.
The combination would strengthen Ambea's position in the Nordic care market, where ageing populations and increasingly complex care needs are driving structural demand.
Humana's board unanimously recommended shareholders accept the offer, while holders of about 41.9% of Humana's shares have undertaken to accept it.
The contingent value right could pay up to SEK 4.36 per Humana share, depending on Humana's appeal in a damages case against the Swedish state over its revoked personal-assistance licence.
Ambea said it plans to divest Humana's Personal Assistance Sweden business following completion of the offer.
($1 = 9.7326 Swedish crowns)
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Reporting by Jesus Calero; Editing by Jamie Freed
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Loopring ukončuje DEX i automatizovaný tvůrce trhu a okamžitě zastavuje veškeré obchodování kvůli slabé adopci a technologickému zastarávání. Tým poté vyplatí zůstatky uživatelům do jejich Ethereum peněženek.
Ethereum’s first zero-knowledge rollup, Loopring, announced Sunday the closure of its decentralized exchange and automated market maker, ending all trading services and halting the relayer effective immediately.
In a post on X on Sunday, the team cited three main reasons for the closure: its failure to gain meaningful adoption, a lack of business development skills and being technologically surpassed by modern zkEVM solutions.
“To be honest, Loopring never gained meaningful adoption,” the team said. “As the first zk-rollup, we lacked a virtual machine – no composability, no real‑world payment use cases. That limitation kept our ecosystem from growing.”
Loopring was a technical pioneer of its time, raising $45 million in a 2017 initial coin offering and helping to prove that scaling Ethereum via zk-rollups was viable. But technology evolves fast in the crypto industry, and it was ultimately surpassed by the more capable successors it helped inspire, such as zkSync, Scroll and StarkNet.
The team said they are “engineers at heart,” not business operators, excelling at writing code but never developing the “passion or skills for business development.”
“External pressures – including major exchange delistings of LRC in 2026 – only accelerated the inevitable,” they said.
The team added that pressure from more advanced competitors, which are fully compatible with Ethereum smart contracts, “while our specialised architecture now feels obsolete,” compounded the decision to gracefully end it, “rather than running a hollow service.”
Loopring had already shut down its wallet services in July 2025, citing scaling challenges.
With the DEX closure, the team said it will be calculating and publishing all final user balances, then distributing funds directly to users' Ethereum wallets in batches and covering gas fees.
Loopring's total value locked is about $8 million, down almost 99% from the $760 million peak in November 2021, according to L2Beat. Its native token, LRC, has collapsed by a similar amount to $0.01 from its all-time high in the same month of $3.75.
Loopring's total value locked has collapsed over the past five years. Source: L2Beat
One of Loopring’s biggest milestones was a 2021 partnership with GameStop to power its NFT platform, launched the following year.
Crypto winter bites deep this yearThe demise of Loopring adds to the growing list of crypto closures this year, as the bear market deepens and previous-cycle narratives no longer apply.
More than 60 crypto projects and protocols have already shuttered services in 2026, according to RootData. Some of the more notable ones include a16z-backed decentralized self-custody solution Entropy, app-chain infrastructure protocol Syndicate and AI blockchain platform Yupp.
Magazine: Bitcoin slides to $58K, XRP hits $1 but onchain data promising: Market Moves
Cointelegraph is committed to independent, transparent journalism. This news article is produced in accordance with Cointelegraph’s Editorial Policy and aims to provide accurate and timely information. Readers are encouraged to verify information independently.
Hong Kong-listed shares of Baidu surged more than 7% Monday on reports that its artificial intelligence chip unit Kunlunxin is targeting an initial public offering in the city, which could value its affiliate at $50 billion.
Prospective investors were asked to buy semiconductors worth three to seven times the value of their intended investment in Kunlunxin's planned listing, The Information reported Sunday, citing two sources familiar with the matter.
Baidu confidentially filed a listing application for Kunlunxin on the Hong Kong Stock Exchange at the start of the year, though offering details, including size and structure, were undecided then.
Kunlunxin chips have drawn interest from ByteDance, the owner of TikTok, according to an earlier Reuters report citing sources.
Founded in 2011, Kunlunxin mainly supplies chips to its parent company Baidu. While Baidu retains a controlling stake, the company operates independently and has broadened its scope to external sales over the past two years.
The report comes as China accelerates efforts to strengthen its position in the increasingly competitive AI sector.
"Despite Chinese progress, the United States remains for now ahead in the race for dominance over the so-called artificial intelligence hardware stack – the resources and equipment, especially semiconductors, needed to run AI models," according to a report by Brussels-based economic think tank Bruegel.
However, the think tank also noted that "the signs of Chinese catch-up are real," citing factors such as an open-sourced toolkit with a state-backed contributor pipeline and a large enough domestic market that could buoy the ecosystem through its immature phase.
Tencent testuje TenPayGo, aplikaci pro zahraniční návštěvníky Číny s mobilními platbami u milionů obchodníků podporujících Weixin Pay. Cílem je umožnit placení bez hotovosti.
China’s Tencent is reportedly testing an app designed for overseas travelers to its country.
TenPayGo was created to function as a one-stop digital services platform that includes mobile payments, Bloomberg News reported Sunday (June 28), citing Jiemian News. The app, now being tested, lets users spend directly at millions of merchants in China that accept Weixin Pay, letting visitors send and explore China with no need for cash, the report added.
Bloomberg noted that China is seeing a steep increase in foreign visitors, with almost 7 billion cross-border trips logged last year, according to the National Immigration Administration. Overseas nationals made up more than 82 million entries and exits, a 26.4% increase compared to the prior year.
The report added that this increase is indicative of expanded visa-free arrangements and wider travel facilitation measures, which authorities say have made it easier for foreign visitors to come to China for both business and pleasure.
Tencent’s efforts come at a time when digital wallets are evolving from “a more convenient way to pay” to “something more consequential: a platform for managing permissions,” as PYMNTS wrote last week.
This evolution can be seen in two recent developments. Samsung’s launch of Samsung ID with CLEAR lets American passport holders store TSA-approved digital credentials inside Samsung Wallet. Meanwhile Visa and OpenAI announced plans to support payments initiated by artificial intelligence agents operating under consumer-defined rules and controls.
“Viewed separately, one initiative concerns identity and the other payments,” PYMNTS wrote. “Together, they point toward a broader development in digital commerce: identity verification and spending authorization are beginning to reside in the same place.”
The report cited data from PYMNTS Intelligence which suggests consumers, younger ones in particular, are already making digital wallets part of their regular shopping behavior, setting the stage for them to get comfortable using them for other things.
The traditional role of digital wallets, the report continued, was to offer users a place to store payment credentials and make checkout simpler. Today’s wallets, however, house boarding passes, loyalty cards, tickets, digital keys and government credentials.
“A wallet that can prove who a consumer is occupies a different position in the commerce ecosystem than one that simply stores a card number,” PYMNTS wrote. “Identity credentials are difficult to establish, heavily regulated and tied directly to fraud prevention and security requirements. Once consumers rely on a wallet for identity verification, the relationship becomes more durable.”
TRM Labs uvedla, že CoinEx od roku 2018 zpracoval s íránskou burzou Nobitex více než 2,7 miliardy USD a celkem přes 3,84 miliardy USD v transakcích se sankcionovanými íránskými subjekty. CoinEx spojení s íránskou vládou odmítá.
CoinEx processed billions in transfers with Iranian exchanges, including more than $2.7 billion in transactions with OFAC-sanctioned Nobitex since 2018.
More than $3.84 billion in blockchain transactions have been traced between crypto exchange CoinEx and sanctioned Iranian entities over a period of more than seven years.
The findings come shortly after the US Treasury’s Office of Foreign Assets Control (OFAC) sanctioned four Iranian exchanges, Nobitex, BitPin, Wallex, and Ramzinex, under Executive Orders 13224 and 13902.
TRM Maps CoinEx’s Expanding Iran Connections According to the latest report by TRM Labs, the four exchanges represented roughly $7.7 billion, or 78%, of Iran’s estimated $10 billion in attributed crypto activity in 2025. Despite repeated enforcement actions, Iran’s annual crypto volumes have remained high. CoinEx, which was founded in 2017 by Haipo Yang and operated through entities in several jurisdictions, has processed more than $79 billion in trading volume.
The exchange has also faced regulatory actions in several countries. TRM’s findings reveal that CoinEx is the largest external counterparty of Iran’s biggest crypto exchange, Nobitex. Since late 2018, more than $2.7 billion has moved between the two platforms through roughly 6.2 million blockchain transfers, averaging about $1 million per day. Nobitex has sent around $360 million more to CoinEx than it received, which suggests that funds are consistently moving from Iran to international markets through CoinEx.
Activity between the two exchanges rose from about $13 million in 2020 to $575 million in 2021. After declining in 2022 and 2023, volumes recovered to $714 million in 2024 and $763 million in 2025. In fact, CoinEx accounted for over 16% of Nobitex’s yearly transaction activity.
TRM also identified direct links between CoinEx and more than 60 Iranian crypto businesses, including Wallex, Ramzinex, BitPin, Aban Tether, Excoino, Bit24, Ompfinex, Sarmayex, and Exir. The report said a similar share of transaction volumes was routed through CoinEx across multiple Iranian exchanges, along with the gradual onboarding of platforms over several years, which points to an organized relationship rather than independent market behavior.
The blockchain intelligence company further found that around $67 million originating from the Central Bank of Iran reached CoinEx through a complex laundering structure between June 2025 and June 2026. Funds reportedly moved through multiple blockchains, cross-chain bridges, Gnosis Safe contracts, and Aave tokens before eventually reaching CoinEx. The exchange also allegedly provided transaction fees that helped support these transfers.
You may also like: Is Bitcoin (And Peace) In Trouble as Trump Warns Iran of Fresh Strikes? BTC, ETH, XRP Progress at Risk as Trump Condemns Israel’s Latest Attacks Will BTC Rocket if Trump Delivers on His Iran Deal Promise This Sunday? ViaBTC, a mining pool operated by CoinEx’s parent company, was also closely tied to Iran. TRM traced more than $154 million between ViaBTC and Nobitex-linked wallets, and most transfers flowed from the mining pool to Iranian wallets. Following the 2025 cyberattack on Nobitex, previously inactive mining wallets transferred about $2.7 million to a new Nobitex wallet. ViaBTC also appeared in the transaction chain, which indicates that mining reserves were used to restore liquidity.
Conflict Altered Transaction Patterns CoinEx’s exposure to wallets linked to the IRGC, Palestinian Islamic Jihad, Hezbollah, Garantex, Bitzlato, the CoinEx hack, BlackSuit ransomware, and the Wasabi mixing service was also found by TRM. Transaction patterns changed after the US-Iran-Israel conflict intensified in early 2026. Average transfer sizes increased sharply, and larger transactions became more common.
After OFAC sanctioned several Iranian exchanges earlier this month, transaction volumes between CoinEx and Iranian entities fell significantly, although the firm noted that private exchange accounts could still allow activity to continue outside public blockchain visibility.
Meanwhile, CoinEx denied having any relationship with the Iranian government or sanctioned entities and said it has never provided funding or support to them. The exchange further asserted that blockchain transactions do not prove involvement in illegal activity.
When investors are searching for high-flying stocks, they likely wouldn't start in the automotive industry. That said, General Motors (GM 0.55%) has been firing on all cylinders over the past three years. The stock is up 116% over that time. Over the past 12 months, it has gained more than 62% compared to the broader S&P 500's 21% rise.
The good news for investors who missed the rise is that GM is poised to keep driving higher for these three reasons.
1. GM is returning value to shareholders Ford Motor Company (F +0.18%) and its Detroit rival, GM, have much in common, but the two return value in distinctly different ways. Ford is well-known for its lucrative dividend, currently yielding roughly 4.2%, and it often dishes out annual supplemental dividends when cash flow is strong.
A GMC Hummer. Image source: General Motors.
Ford gets more attention for the value it returns through its dividend than GM does for its buybacks, but GM's buybacks are quietly impressive. More specifically, over the past five years, GM has slashed its shares outstanding by a huge chunk, as you can see in the graph below.
Data by YCharts.
Thanks to high-margin, lucrative full-size truck sales and valuable SUV sales, the company generates significant cash. It's used this cash to fund development of a long list of new vehicle launches, and has also retired roughly 500 million shares valued at $30 billion over the past five years -- a staggering number.
While rival Ford's dividend yield sits at roughly 4.2%, much higher and more recognizable than GM's 0.9% dividend yield, the latter's total shareholder yield (which adds buybacks into the equation) sits at a much more impressive 7.6%. Expect GM to continue its buyback strategy, and more investors should be aware of just how valuable it is.
2. GM's OnStar is on point Another factor that many investors overlook with General Motors is its ongoing bet with OnStar and Super Cruise. The automaker is making a long-term bet that it can generate meaningful recurring revenue through its software business.
Last year, GM logged roughly $2.7 billion in realized revenue. It has an even larger $5.4 billion in deferred revenue from OnStar and Super Cruise subscriptions. For context, that's real growth from the $1.7 billion realized and $200 million deferred as recently as 2020. There's more growth ahead, with the company expecting to generate $3.1 billion in realized revenue and $7.5 billion in deferred revenue this year.
Here's the kicker: Starting with 2025 model years, GM is including an eight-year subscription to OnStar services, as well as a three-year subscription to Super Cruise. The simple strategy behind this is gambling that when people go to purchase their next vehicle, they will have become so used to these services that they'll purchase them again. There is some evidence already that this strategy is working: At least 30% of the 35,000 GM owners who had expiring three-year subscriptions to Super Cruise resubscribed last year. These are high-margin sales, comparable to those seen in the software industry.
3. GM's vehicle model balancing act has been successful Most investors are aware that almost everyone in the automotive industry misjudged electric vehicles (EVs) and how quickly they anticipated the shift in demand trends. This caused the broader industry to take billions and billions in charges to rebalance between production and capacity between EVs and traditional gasoline-powered vehicles. GM was no exception, taking a special items hit of $7 billion in the fourth quarter of 2025.
While EVs are largely unprofitable and continue to hinder most automakers' earnings, GM has invested much time, effort, and capital into LMR battery chemistry that is expected to reduce cell and battery pack costs by several thousand dollars per unit. That puts GM on the path to EV profitability, which management expects to achieve within three to five years, reversing billions in annual losses. Reversing EV losses is arguably the easiest way for GM to boost its bottom line and reward investors with an appreciating stock price -- and, likely, a better valuation.
Today's Change
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What it all means GM has quietly been thriving for the better part of the past decade, and has managed to talk Wall Street into rewarding it with a price-to-earnings ratio in the lower 30x. That's rare for automakers, which are typically valued around 10x price-to-earnings. That's simply because the automaker is well-positioned to continue thriving in the years ahead, for the three reasons stated above, among others. GM is far from the Detroit automaker of old, and don't be surprised if it keeps beating the broader market over the next three to five years.
Ministerstvo spravedlnosti USA ukončilo trestní vyšetřování společnosti Abbott Laboratories kvůli závodu na výrobu kojenecké výživy a namísto toho zvažuje civilní sankce. Firma v roce 2022 stáhla produkty z trhu a uzavřela michiganský závod po nálezu potenciálně smrtelné bakterie.
Abbott's milk powder products are displayed on a shelf at a supermarket in Beijing August 7, 2013. Abbott Laboratories has agreed to pay a fine amounting to around $12 million, a spokeswoman... Purchase Licensing Rights, opens new tab Read more
CompaniesJune 28 (Reuters) - The U.S. Justice Department closed a criminal probe into Abbott Laboratories (ABT.N), opens new tab over its handling of a baby formula plant linked to potentially deadly bacteria and infant deaths, opting instead for civil penalties, the Wall Street Journal reported on Sunday.
Reuters could not immediately verify the report. The U.S. Department of Justice and Abbott Laboratories did not immediately respond to a request for comment outside business hours.
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Abbott initiated a recall of its infant formula products and closed its Michigan plant in 2022 after investigators found traces of a potentially deadly bacteria at that plant. The recall and the plant closure worsened a national shortage of baby formula that had begun with pandemic supply chain issues.
Abbott had said at the time that there was no evidence linking its formulas to these illnesses. No unopened, distributed Abbott infant formulas have tested positive for the bacteria that sickened the babies, a company spokesman told the WSJ.
Some prosecutors believed they had evidence to criminally charge the company, but top decision makers closed the probe, according to the WSJ report. Instead, they opted for the lighter option of clawing back money the company earned from selling formula through federally funded nutrition programs, the report added.
“Ensuring the safety of our nation’s food supply is a top priority for the Trump administration; however, this Department of Justice does not believe in regulation by prosecution,” a spokeswoman for the DOJ told WSJ.
Prosecutors had been considering a misdemeanor charge against Abbott for violating the federal Food, Drug and Cosmetic Act and a separate count for misleading the government before dropping the case, the report said, and added that prosecutors were also considering charging at least one individual.
Reporting by Akanksha Khushi in Bengaluru; Editing by Rashmi Aich
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HP Inc. oznámila strategické partnerství s OpenAI a začne v podniku nasazovat platformu Frontier napříč svým byznysem. HP patří mezi první globální podniky, které ji přijaly.
HP Inc. will deploy powerful AI-driven solutions with OpenAI Frontier to help drive HP transformation and growth initiatives The Frontier platform will be used across HP’s business, to enhance customer-facing experiences and internal operations The Frontier strategic partnership supports HP’s efforts to deliver an advanced telemetry platform with WXP, a recognized Gartner magic quadrant leader, enabling a connected device layer for the AI era PALO ALTO, Calif., June 28, 2026 (GLOBE NEWSWIRE) -- Today, HP Inc. (NYSE: HPQ) announced the launch of a strategic partnership with OpenAI, integrating its Frontier platform into HP’s global efforts to shape the Future of Work through enhanced customer-facing experiences and accelerated transformation across its operations.
“With OpenAI there is an opportunity to fundamentally rethink how AI can deliver better outcomes. With the use of Frontier platform, HP is planning to build a more consistent experience across store, partner, chat, and voice experiences, giving customers and partners faster ways to get answers, complete routine workflows, and move toward resolution. It reflects the ambition of our AI strategy to deliver real-world outcomes at scale,” said Prakash Arunkundrum, chief strategy and transformation officer, HP Inc.
HP has become one of the first global enterprises to adopt the Frontier platform to fuel its transformation. While specific use cases will be refined and added as the strategic partnership rolls out, HP’s aim is to deploy AI-driven solutions across areas that include:
Customer- and partner-facing solutions and experiencesCustomer telemetry insights, enabled through HP’s market leading WXP solution, and reportingEmployee productivity Software development “HP is showing what enterprise transformation looks like when AI becomes an operating layer - connected to the systems and workflows where work already happens,” said Denise Dresser, chief revenue officer at OpenAI. “HP has been an exceptional early partner, turning early value from OpenAI APIs and tools like ChatGPT and Codex into repeatable systems. We're thrilled to go deeper with them as they move beyond Frontier pilots to deliver measurable business impact at scale.”
The launch of the Frontier strategic partnership follows an exploratory period started in February 2026, in which HP worked with OpenAI to conduct a comprehensive evaluation of Frontier and its capabilities. HP assessed technical capabilities, use cases, and strategic alignment with company priorities through pilots of agentic capabilities, platform components, security, and enterprise integration.
Based on this evaluation, HP has determined OpenAI offers best-in-class models with a compelling vision for agent-based capabilities. With the Frontier strategic partnership underway, the two companies now plan to co-develop future use cases and ensure they meet HP’s rigorous enterprise standards, particularly around data integration, governance, and security. For HP, AI is becoming a new layer for how work gets done across the company. With OpenAI Frontier, that layer is being built with the context, governance, and execution capacity needed to move from early wins to enterprise-wide transformation.
Shaping the Future of Work for the AI Era
AI will change how people work. As AI tools get more powerful, HP believes that humans and AI agents will work together to unlock a new era of innovation and productivity. To prepare for this future, HP is innovating a suite of agentic AI Devices that seamlessly integrate into existing workflows, increasing employee efficiency. For AI Workloads that require always-on inference, HP is building devices with dedicated hardware optimized to run agentic AI workloads 24x7, creating the technology layer customers need to achieve their AI vision.
HP’s customers are building their workspaces to include PCs, workstations, printers, and collaboration solutions that work together to deliver powerful AI experiences, all secured and managed by the Workforce Experience Platform (WXP). WXP, a Leader in the 2026 Gartner® Magic Quadrant™ for Digital Employee Experience Management Tools, offers a ‘single pane of glass’ that can manage entire fleets of devices and provide the peace of mind CIOs and IT managers need as they define this AI future for their organizations.
HP is the surface where work gets done. As we move into an AI-driven era of technological advancement, HP brings AI to the edge, where work happens — not just where data is processed. That is the future of work.
About HP
HP Inc. (NYSE: HPQ) is a global technology leader redefining the Future of Work. Operating in more than 180 countries, HP delivers innovative and AI-powered devices, software, services, and subscriptions that drive business growth and professional fulfillment. For more information, please visit: HP.com.
Forward-Looking Statements
This press release contains forward-looking statements based on current expectations and assumptions that involve risks, uncertainties, and assumptions. If the risks or uncertainties ever materialize or the assumptions prove incorrect, the results may differ materially from those expressed or implied by such forward-looking statements and assumptions. All statements other than statements of historical fact are statements that could be deemed forward-looking statements, including, but not limited to, statements regarding the partnership between HP and OpenAI, the expected benefits of the partnership, the impact of the partnership on HP’s business, future opportunities, and any other statements regarding HP’s future expectations, beliefs, plans, objectives, or future events or performance. Forward-looking statements can also generally be identified by words such as “future,” “anticipates,” “believes,” “estimates,” “expects,” “intends,” “plans,” “predicts,” “projects,” “will,” “would,” “could,” “can,” “may,” and similar terms. Our forward-looking statements involve significant risks and uncertainties (may of which are beyond HP’s control) including the factors described in the Annual Report on Form 10-K for the fiscal year ended October 31, 2025, and HP’s other filings with the Securities and Exchange Commission. The forward-looking statements in this press release are made as of the date of this document and HP assumes no obligation and does not intend to update these forward-looking statements.
Tesla má v prvních dnech července zveřejnit údaje o dodávkách za 2. čtvrtletí; trh sleduje hlavně meziroční růst. Konsensus čeká asi 406 000 vozů, což by bylo nad loňskými 384 122.
Tesla (TSLA +1.38%) is set to report its second-quarter vehicle deliveries in the first days of July -- something that will draw attention away from its more aspirational ventures like robotaxis and humanoid robots. The most important figure from the production and delivery update will likely be the year-over-year growth rate in deliveries.
The update will be timely, as deliveries are the most direct measure of whether demand for Tesla's cars is recovering after a difficult 2025 -- and this quarter is the first meaningful test of whether that recovery has staying power.
In 2025, Tesla delivered 1,636,129 vehicles, down 8.6% from nearly 1.8 million in 2024. The first quarter of 2026 brought a return to growth, with deliveries rising 6.3% year over year to 358,023. But there was a complication: Tesla produced about 50,000 more vehicles than it delivered -- a larger-than-usual gap between supply and demand that likely worried some investors.
So, can Tesla report a strong enough year-over-year growth rate to convince investors that a sustainable rebound in the company's automotive business is underway?
Tesla Cybercab. Image source: Tesla.
Here's the threshold Tesla needs to cross Wall Street's consensus calls for about 406,000 deliveries in the second quarter. Some of the more bullish forecasts run higher, at about 420,000. Either would clear the comparison that matters most: the 384,122 vehicles Tesla delivered in the second quarter of 2025.
Climbing back above that year-ago level would mean Tesla has put together two straight quarters of growth.
So, here's a simple way to frame the report: A number around 406,000 or higher would arguably signal that a meaningful recovery is on track. A figure near or above 420,000 would suggest momentum is building faster than expected. But a result that slips back toward last year's 384,122 would support the bear case, showing that the first-quarter bounce was temporary and that demand still isn't keeping pace with Tesla's production.
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Where the number gets decided While Tesla doesn't break out regional deliveries in its quarterly production and deliveries update, regional performance will be key to the overall figure.
Europe has reportedly recently turned from a weak spot into a source of growth for the company; Tesla's new-car registrations there more than doubled year over year in May, a sharp reversal from the steep declines that weighed on 2025. China, Tesla's second-largest market, has also reportedly held up well, helped by the refreshed Model Y.
The drag, however, may be the United States. With the tax credit having expired at the end of the third quarter of 2025, U.S. demand has cooled, and registrations there have reportedly tracked down by the mid-teens so far this year. So the second-quarter number probably comes down to one question: Is the strength in Europe and China enough to more than offset any domestic softness?
Still, even though the reported year-over-year growth rate for Tesla's deliveries will be an important figure to watch, it's clear that investors buy the stock for far more than its automotive business. After all, that's the only thing that could explain its astronomical valuation. Tesla stock trades at about 345 times earnings -- a multiple that only makes sense if investors are paying for self-driving software and robots rather than for simply electric cars.
But the car business still generates the majority of Tesla's revenue, so a soft delivery number would be a reminder of how far the company is from growing into its wild valuation.
Tesla shares are down about 16% so far in 2026, trading well below their December high near $490. So you can bet investors are hoping for some good news. With that said, the more important update will probably come later in July, when the company reports its full second-quarter results, which will include financials like revenue and cash flow, as well as the company's progress on its important Robotaxi operation and its longer-term ambitions, such as humanoid robots.
Shopify uzavřel partnerství s Trustpilot, které obchodníkům umožní zobrazovat a spravovat recenze přímo v internetových obchodech. Integrace má být spuštěna v pondělí 29. června.
Reviews website Trustpilot has reportedly launched a partnership with eCommerce platform Shopify.
The arrangement will let merchants showcase and manage Trustpilot reviews on their online stores, Bloomberg News reported Saturday (June 27), citing an interview with Adrian Blair, Trustpilot’s chief executive.
Blair said that third-party consumer feedback is growing in importance as artificial intelligence plays a larger role in online retail.
“The key problem that all these Shopify merchants are facing is, how do you actually build trust with customers now in the age of AI?” he said. “There is so much that is now being created by AI, this kind of synthetic content, and Trustpilot is a canonical source of what people say about their experiences with businesses.”
AI-driven search engines and AI shopping assistants also depend on data such as Trustpilot’s, the report added, meaning that a greater volume of reviews can create more visibility online. Trustpilot content is already a vital resource for large language models, with the click-through rate from AI search climbing 1,490% in its most recent financial year, Bloomberg said.
Integrated Trustpilot reviews on the Shopify platform are set to go live Monday (June 29), the report continued. Blair had said in March that his company was exploring partnerships with the internet’s shopping giants.
The Shopify collaboration is “the first kind of major proof point, so we are executing against the strategy that we set out earlier this year,” Blair told Bloomberg, adding that the agreement isn’t exclusive and Trustpilot hopes to pursue partnerships across a variety of industries.
“We see huge adoption of Trustpilot with banks, insurance companies, utilities, accounting firms, cybersecurity companies, law firms, et cetera,” Blair added. “For us retail is very important, but it is one of many verticals.”
Meanwhile, recent research from PYMNTS Intelligence shows that consumers want AI to be involved in their online shopping journey, though more as a navigator than a driver.
“Tasks involving discovery, comparison shopping and information gathering emerged as natural fits for AI,” PYMNTS wrote earlier this month. “Areas involving payments, financial commitments and irreversible decisions, however, continued to trigger greater demand for human oversight.”
The findings, from the May 2026 Consumer AI Benchmark, indicate that the next phase of AI adoption will hinge less on the sophistication of the technology and depend more on whether merchants can find the balance between automation and human control.
Nvidia (NVDA 1.42%) has become almost synonymous with the words "artificial intelligence" (AI). When people think of AI, they automatically think of this company -- and for good reason. Nvidia has generated quarter after quarter of explosive earnings growth, with revenue and profit reaching record levels, thanks to its AI products.
The company is the world's leading designer of graphics processing units (GPUs), the powerful chips used to fuel AI tasks, and has expanded across other related products, such as networking tools and enterprise software, to build complete AI systems.
Investors recognized Nvidia's strength in AI and raced to get in on this exciting growth story. The result? Nvidia stock soared more than 1,100% over the past three calendar years.
Of course, investors are always on the lookout for another stock that may perform as well. They may not have to look very far. Micron Technology (MU 6.59%) has proven itself to be an AI heavyweight, providing the memory and storage crucial for AI use. Is Micron stock the new Nvidia? Let's find out.
Image source: Getty Images.
Increasing earnings over time Micron isn't new to the technology scene. The company got its start almost 50 years ago and has served computers and other devices with a portfolio of memory and storage options. This helped the company increase earnings over time, but at a much slower pace than what we're seeing today.
MU Net Income (Quarterly) data by YCharts
Though Micron has seen business ebb and flow in the past, as is normal in the cyclical semiconductor industry, the current surge is a whole new ball game. Needs linked to AI have supercharged growth, as we've seen in recent quarters. The latest is the perfect example, with revenue more than quadrupling to reach past $41 billion and net income jumping from $1.8 billion in the year-earlier period to an eye-popping $28 billion.
On top of this, Micron says that demand is surpassing supply, and the company expects this to continue beyond this calendar year. This supply situation is due to strong AI demand as well as general supply constraints that are impacting the entire memory industry. These include various factors, including the time it takes to ramp up manufacturing facilities and obtain permits, and a complex regulatory framework.
While this is a challenge for Micron, it also means that competition isn't a major problem: There is more than enough business for each of the top players to generate growth.
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How Micron resembles Nvidia Now, let's consider how Micron may resemble Nvidia. Like Nvidia, it plays a key role in the AI growth story. The company offers the DRAM, NAND, and HBM memory products that are crucial to the functioning of the technology. And we can imagine that, as the use of AI agents increases, the need for memory power may become even greater. Agentic AI, seen as the next AI growth driver, involves AI taking action, often through several steps, to solve problems.
Also like Nvidia, Micron has been around for decades, perfecting its products, and today, both companies have achieved extremely high profitability on sales. In fact, Micron's gross margin just surpassed that of Nvidia. Micron's reached more than 84% in the recent quarter, while Nvidia's gross margin tops 74%. So not only are these players benefiting from revenue growth in the AI boom, but they are translating that into significant profit.
One area that separates the two is the following: Nvidia is the AI chip leader and has expanded into related products, as mentioned above. Micron remains a memory and storage specialist -- and in AI, though Micron is growing fast and is among the leaders, South Korea's SK Hynix often is seen as the AI memory giant.
This doesn't necessarily mean Micron won't take the path of Nvidia, from an earnings and stock performance perspective. It does mean the company might come with a bit more risk, though.
Now, let's consider stock performance. Micron is already well on its way along an Nvidia-like path. The stock has soared more than 800% over the past year. So I think Micron might already be the next Nvidia -- and the demand and revenue growth Micron has seen in recent months suggest the stock still may have plenty of room to run over the long term.
AST SpaceMobile plánuje v první polovině srpna 2026 vypustit BlueBirdy 11, 12 a 13, což má posílit jeho satelitní síť. Nové satelity mají téměř zdvojnásobit dosavadní rekordní rychlost 98,9 Mb/s.
AST SpaceMobile (ASTS +9.08%) has already proved that ordinary phones can connect directly to satellites. The bigger test now is whether it can build, launch, and operate enough of its BlueBird satellites to turn that technology into a commercial network.
Here's why its upcoming satellite launch could strengthen the bullish case for the stock and why buying before the planned August launches makes sense.
Image source: Getty Images.
AST SpaceMobile's satellite launch strategy In June 2026, AST SpaceMobile launched BlueBirds 8, 9, and 10, which the company says are already operating in orbit. It is now targeting the launch of BlueBirds 11, 12, and 13 in the first half of August 2026.
This timeline will test whether AST can keep launching satellites at the pace needed to build a commercial network. The satellites due to be launched in August are expected to use large 2,400-square-foot antennas.
The company recently reached a peak download speed of 98.9 megabits per second from its satellite network directly to ordinary smartphones. The August satellites are expected to nearly double that peak speed.
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In the 2026 first-quarter earnings call, management said that BlueBird satellites 11 through 33 were already in an advanced state of assembly, with key antenna parts completed through BlueBird 28. The company is targeting six fully assembled satellites per month, showing that it is trying to move from building satellites one by one to a steadier launch program.
AST SpaceMobile says it has already contracted launch capacity to support its 2026 target of roughly 45 satellites in orbit. The company is not relying on only one rocket provider. Its launch plan includes Space Exploration Technologies' Falcon 9, which can carry three BlueBird satellites; Blue Origin's New Glenn, which can carry up to eight; and United Launch Alliance's Vulcan, which can carry up to five. The alliance is a joint venture between Boeing and Lockheed Martin.
Management said new satellites could be ready to support 4G or 5G service with mobile network partners about 45 days after launch. Over time, it aims to cut that setup period to about two weeks.
Financials may improve over time AST SpaceMobile's revenue was only $14.7 million in the first quarter. However, management expects revenue to grow in the remaining three quarters of 2026. The company is guiding for 2026 revenue in the range of $150 million to $200 million.
The revenue story goes beyond satellite launches. AST SpaceMobile expects 2026 revenue from ground equipment and services for mobile-network partners, government contract work, consulting with mobile operators, and possible early service revenue as more satellites are launched and activated.
Management sees 2027 revenue potentially approaching $1 billion, helped by cellular broadband service in major markets and larger U.S. government contracts. To support that growth, the company is working on ground networks across markets covering about 2.9 billion people. This groundwork should help mobile-network partners activate service as more satellites come online.
Lastly, AST had about $3.5 billion in cash on its balance sheet at the end of the first quarter, against about $3.02 billion of total debt. Since nearly $2.9 billion of that is long-term debt, AST SpaceMobile has some flexibility to fund its commercial strategy.
I think it makes sense to buy the stock before the August launches.
CoreWeave má backlog 99,4 miliardy USD a v prvním čtvrtletí mu výnosy vzrostly o 112 % na 2,1 miliardy USD. Firma zároveň zvýšila smluvní kapacitu datacenter na 3,5 GW.
Nvidia invested $2 billion in neocloud infrastructure provider CoreWeave (CRWV 2.27%) in January this year to help the latter build artificial intelligence (AI) factories powered by its chips. That investment has appreciated 11% since then despite bouts of volatility.
However, it won't be surprising to see this AI stock jump higher in the future, as it plays an important role in the AI infrastructure ecosystem by building dedicated AI data centers. Let's look at the reasons why this fast-growing company could be an ideal addition to your portfolio right now.
Image source: The Motley Fool.
CoreWeave's enormous backlog is going to fuel years of terrific growth Cloud computing giants such as Meta Platforms and Microsoft have been spending heavily on building AI data centers. Microsoft reported remaining performance obligations (RPO) of $627 billion in the previous quarter, nearly doubling year over year due to increasing demand for its AI services. Meta, on the other hand, is spending big on data center infrastructure to build AI products for customers and advertisers.
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CoreWeave has been the beneficiary of their aggressive capital spending, landing massive contracts to provide data center capacity for these companies. However, CoreWeave's customer base extends beyond these hyperscalers, as the likes of OpenAI and Anthropic have also turned to CoreWeave to build data centers.
In fact, CoreWeave noted in its May earnings call that it has 10 customers who have committed to spending at least $1 billion each to rent data center capacity from the company. Moreover, CoreWeave is diversifying its customer base by adding financial services clients, such as Jane Street and Hudson River Trading. It has also added other pure-play AI companies, such as Perplexity AI, to its client list.
Goldman Sachs predicts that data center power demand in the U.S. is going to double by next year, rising to 66 gigawatts (GW) from 31 GW in 2025. Not surprisingly, AI companies and hyperscalers have been quickly buying the available data center power capacity from the likes of CoreWeave.
This explains why CoreWeave's revenue backlog sits at a remarkable $99.4 billion, with the metric growing by 284% year over year in Q1. For comparison, the company's quarterly revenue rose 112% to $2.1 billion. That revenue growth rate will accelerate sharply as CoreWeave builds more data centers.
The company's active data center power capacity crossed the 1 GW mark in Q1. Importantly, it increased its contracted power capacity to 3.5 GW. The contracted capacity is the electrical power that CoreWeave has secured from utility providers to build AI data centers. This suggests CoreWeave can more than triple its active capacity in the future. What's worth noting is that CoreWeave aims to build 8 GW of active data center capacity by the end of the decade.
Of course, building AI data centers is a capital-intensive endeavor, which explains why CoreWeave has been taking on significant debt to fund its expansion. As a result, its interest expense doubled year over year in Q1 to $536 million. CoreWeave has raised $20 billion this year through debt and equity financing, suggesting that interest expenses will continue to weigh on its bottom line.
However, the company is trying to lower financing costs, with management pointing out that it is "broadening access to capital at lower blended cost will continue to be an important lever for CoreWeave as we convert backlog to revenue and operating cash flow." CoreWeave estimates that it will convert 36% of its backlog into revenue over the next two years, while 75% of the backlog is likely to be recognized as revenue over the next four years.
As a result, CoreWeave expects its annualized run rate revenue to jump from $18 billion at the end of 2026 to $30 billion at the end of 2027. The aggressive conversion of CoreWeave's backlog into revenue will also boost its bottom line.
Data by YCharts
Here's why this stock looks like a potential multibagger CoreWeave stock has jumped by 22% in 2026, which helps explain why it can still be bought at just under 8 times sales, which isn't very expensive considering that the tech-focused Nasdaq Composite index has a price-to-sales ratio of 5.2. The slight premium it trades at can be justified by its ballooning backlog, triple-digit revenue growth, and the ability to sustain solid growth in the future.
Data by YCharts
If CoreWeave's top line indeed jumps to $40 billion by the end of 2028 and it trades at the Nasdaq Composite's sales multiple, its market cap could increase to $208 billion. That's significantly higher than its current market cap of $53 billion, indicating that this growth stock could become a multibagger. That's why buying CoreWeave seems like a no-brainer right now, as it is pulling the right strings to capitalize on the booming demand for AI data centers.
Bitwise převedl 1.775 milionu HYPE do stakingu, což při transakční ceně odpovídá zhruba 114 milionům dolarů. Krok posiluje jeho sázku na Hyperliquid i nový ETF BHYP.
Bitwise brutally strengthens its crypto bet on Hyperliquid. The asset manager transferred 1.775 million HYPE tokens to the protocol before staking them. The operation, estimated at around 114 million dollars, accompanies the rise of its Hyperliquid spot ETF launched in May.
In brief Bitwise placed 1.775 million HYPE in staking. The crypto operation amounts to about 114 million dollars. The BHYP ETF strengthens institutional demand around Hyperliquid. Bitwise deposited 1.775 million HYPE on Hyperliquid, then committed all the tokens to staking. This position confirms the interest already shown by the manager for an asset he recently judged undervalued on the market.
At the price taken during the transaction, the tokens represented roughly 114 million dollars. This is therefore no longer a simple institutional test. Bitwise is establishing massive exposure on one of the main decentralized crypto derivatives platforms.
Staking also reduces the amount of HYPE immediately available on the market. When large holders lock their tokens, the liquid supply can contract. This mechanism however does not guarantee an automatic price increase. The economic model of Hyperliquid plays a central role in this operation. Staking rewards are not only based on the issuance of new tokens. They are notably supported by the activity and revenue generated by the protocol.
Bitwise is thus exposed to two crypto variables. The first remains the price of HYPE. The second depends on Hyperliquid’s level of use, notably the volume handled on its decentralized markets. This structure makes the bet more strategic than a classic purchase. If the activity grows, the protocol’s revenues can reinforce staking interest. Conversely, a drop in volumes would reduce the position’s economic attractiveness.
Hyperliquid quickly established itself in derivatives trading. The platform now competes with several major centralized venues on certain indicators, while retaining a largely on-chain architecture.
The BHYP ETF fuels crypto accumulation The operation follows the launch of the Bitwise Hyperliquid ETF, listed under the symbol BHYP. This product gives investors exposure to HYPE without forcing them to directly manage a crypto portfolio or technical staking constraints.
The fund also seeks to capture rewards thanks to the tokens held. This design distinguishes BHYP from an ETF that would merely passively track the price of an asset. Bitwise wants to combine market exposure and on-chain yield.
The manager also dedicates part of its revenue to buying and staking HYPE. Fund growth can therefore feed new demand for the token. The more assets managed increase, the larger this mechanism can grow.
This dynamic explains why the Hyperliquid ETF now occupies an important place in Bitwise’s crypto strategy. The manager no longer only bets on Bitcoin or Ethereum. It also seeks to capture growth from younger infrastructures.
Hyperliquid attracts institutional finance Bitwise is not alone in this field. Other managers have also sought to launch products linked to HYPE. This competition shows Hyperliquid has exceeded its status as a platform reserved for specialized traders.
The arrival of regulated funds can create a new source of demand. A few tens of millions of dollars represent little at the scale of traditional finance, but a lot for a token whose liquid supply remains limited. This concentration carries risks though. If ETFs accumulate a large share of available HYPE, their purchases can support the price. But their sales could also amplify a correction during massive exits.
Staking adds another level of dependency. Bitwise must monitor the protocol’s operation, validators, technical risks, and the network’s rule evolution. Institutional exposure does not remove crypto’s inherent vulnerabilities.
The 114 million dollar investment thus remains a strong signal, but not a guarantee. It confirms that Hyperliquid is entering a new phase, driven by ETFs, staking, and institutional capital. The battle for exposure to HYPE is probably just beginning, while the token aims higher in the crypto hierarchy.
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Evans S.
Fascinated by Bitcoin since 2017, Evariste has continuously researched the subject. While his initial interest was in trading, he now actively seeks to understand all advances centered on cryptocurrencies. As an editor, he strives to consistently deliver high-quality work that reflects the state of the sector as a whole.
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The views, thoughts, and opinions expressed in this article belong solely to the author, and should not be taken as investment advice. Do your own research before taking any investment decisions.
Hyperliquid překonal S.A.N.T.A v 24hodinových příjmech a jeho kumulované příjmy už přesáhly 1,027 miliardy USD. Až 97 % poplatků jde na zpětné odkupy HYPE.
Hyperliquid has overtaken S.A.N.T.A in 24-hour revenue generation, marking another data point in the ongoing battle between competing memecoin infrastructure models.
The platform, which runs its own Layer-1 blockchain purpose-built for perpetual futures trading, has turned itself into one of DeFi’s most efficient revenue engines. Cumulative revenue has surpassed $1 billion, reaching roughly $1.027 billion according to DefiLlama data.
The revenue flywheel that keeps spinning Hyperliquid captures trading fees and funnels them into what it calls an Assistance Fund. That fund exists primarily for one purpose: regular buybacks of HYPE, the platform’s native token. Up to 97% of fees get redistributed into these buybacks.
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Annualized revenue run rates currently sit between $676 million and $843 million. Hyperliquid has at times generated more revenue than Ethereum. The platform operates without venture capital funding and runs a minimal team.
S.A.N.T.A and the transparency question Public information about S.A.N.T.A’s operations, revenue metrics, and overall business model remains difficult to verify independently. There are no public sources confirming the operational functionality or revenue claims of S.A.N.T.A as related to Hyperliquid.
Hyperliquid’s revenue figures are trackable through DefiLlama and other on-chain analytics tools.
What this means for investors Hyperliquid’s perpetual futures focus gives it a structural advantage. Perps are the most traded instrument in crypto, often generating multiples of spot trading volume.
The HYPE buyback mechanism, funded by up to 97% of fees, creates consistent demand pressure on the token. The 97% redistribution rate also leaves very little cushion for building reserves or funding development during lean periods.
Disclosure: This article was edited by Editorial Team. For more information on how we create and review content, see our Editorial Policy.
Bitcoin se blíží vzácnému týdennímu death crossu, který dříve předcházel dalšímu 28% poklesu. Michael Saylor zároveň naznačil další nákupy BTC, i když má Strategy poprvé v tomto cyklu mNAV pod 1,0.
TLDR:Bitcoin Weekly Death Cross Raises Fresh BTC Price ConcernsMichael Saylor Hints at More Bitcoin Buying Despite Strategy Valuation Pressure Bitcoin approaches a rare weekly death cross as traders monitor long-term market direction closely. Strategy’s mNAV has dropped below 1.0 for the first time during this market cycle. Michael Saylor hinted at more Bitcoin discussions despite growing valuation concerns. Technical signals and institutional buying remain key factors shaping Bitcoin sentiment. Bitcoin could soon print a rare weekly death cross as bearish technical signals return to the market. At the same time, Michael Saylor has hinted that Strategy may continue accumulating Bitcoin despite growing pressure on its valuation.
The two developments have reignited discussion around Bitcoin’s price outlook and institutional demand. Investors are now watching technical charts alongside corporate buying activity for the next major market signal.
Bitcoin Weekly Death Cross Raises Fresh BTC Price Concerns Crypto Rover shared that Bitcoin is approaching a weekly death cross, a technical pattern that appears when the long-term moving average falls below the shorter trend. The account noted that the previous weekly death cross preceded another 28% decline in Bitcoin’s price.
🚨 BITCOIN WEEKLY DEATH CROSS IS NOW INCOMING.
Last time this happened, BTC crashed another -28%.
If history repeats again, the real bottom may not come until late Q3 or early Q4 2026.
That would also perfectly match Bitcoin’s 4-year cycle. https://t.co/NgE8PlCamN pic.twitter.com/sbPGjGTIv4
— Crypto Rover (@cryptorover) June 28, 2026
The same post highlighted Bitcoin’s historical four-year market cycle. According to Crypto Rover, another extended correction could align with the later stages of the current cycle if previous patterns repeat.
The signal has attracted attention because weekly chart formations appear far less often than daily indicators. Traders typically monitor them for broader market direction rather than short-term volatility.
Despite the technical setup, the pattern alone does not determine future price action. Market participants continue weighing macroeconomic conditions, liquidity, and institutional demand alongside historical chart behavior.
Michael Saylor Hints at More Bitcoin Buying Despite Strategy Valuation Pressure While bearish technical signals circulated, Michael Saylor posted that more charts would be needed, a familiar response that often precedes fresh Bitcoin discussions. His comment followed renewed debate surrounding Strategy’s ability to continue funding Bitcoin purchases.
🚨 JUST IN: Michael Saylor hints at buying more $BTC.
What's interesting is the timing.
Strategy's mNAV has now fallen below 1.0 for the first time this cycle, meaning the company is trading below the market value of the Bitcoin it holds.
Management has previously indicated… https://t.co/WkFYTYOyBi
— Wise Advice (@wiseadvicesumit) June 28, 2026
Wise Advice pointed to Strategy’s market value relative to its Bitcoin holdings. The account noted that the company’s modified net asset value, or mNAV, has fallen below 1.0 for the first time during the current market cycle.
According to the same discussion, Strategy previously suggested that issuing new equity below roughly 1.22 times mNAV could reduce shareholder value. That threshold has prompted questions about whether additional equity-funded Bitcoin purchases remain practical under current market conditions.
Even so, Saylor’s brief response has kept attention on Strategy’s long-standing Bitcoin accumulation strategy.
Investors now await any official filings or announcements that could clarify whether another Bitcoin purchase is approaching while the company navigates changing market dynamics.
El Salvador koupil dalších osm bitcoinů a zvýšil své rezervy na 7 696,37 BTC. Nákupy pokračují i po změnách pravidel, které zrušily povinnost přijímat bitcoin jako platbu.
Bitcoin continues to hold an important place in El Salvador’s financial strategy, which continues its regular purchases despite changes in its regulatory framework. The country has just added new digital assets to its national treasury, confirming the continuity of its reserve policy. This new acquisition comes as sovereign cryptocurrency reserves remain closely monitored by market observers and institutional players around the world.
In brief El Salvador purchased eight new bitcoins, bringing its national reserves to 7,696.37 BTC. The country continues its weekly accumulation strategy despite recent changes to its legislative framework. The new rules remove the obligation to accept Bitcoin as a means of payment without affecting the national reserve policy. Regular acquisitions continue to strengthen El Salvador’s treasury, whose sovereign reserves remain closely monitored. El Salvador Continues Its Accumulation Strategy El Salvador has strengthened its national bitcoin treasury by acquiring eight additional units during the past week. This operation now brings public reserves to 7,696.37 BTC, according to the official data from the Ministry of Finance.
The government thus maintains a regular purchase pace, which has become a component of its digital asset management strategy. This progression confirms the country’s intention to pursue its accumulation plan without interruption.
Moreover, the Bitcoin Office continues to monitor the evolution of national reserves through public data. This transparency makes it possible to measure each new acquisition made by the authorities. Several observers have also relayed this recent increase in sovereign holdings. El Salvador remains among the states whose digital asset reserves receive constant attention.
Bitcoin Retains a Place in the National Strategy Despite IMF Reforms The latest purchase comes after several adjustments made to the legal framework regarding Bitcoin, as part of the agreement concluded with the International Monetary Fund (IMF). The adopted changes mainly concern its use in daily commercial activities. Private companies are no longer obliged to accept this asset as a means of payment. However, Bitcoin remains integrated into the legal framework implemented by the authorities.
At the same time, the national reserve policy has not experienced any interruption. Official data show that weekly purchases continue according to the same logic as before. This separation between payment policy and reserve strategy now appears clearer. El Salvador therefore continues to develop its holdings while adapting certain rules governing the use of the digital asset.
A National Reserve That Keeps Progressing Each new acquisition gradually increases the volume of public reserves of the country. With a total of 7,696.37 BTC, El Salvador confirms the continuity of its long-term accumulation policy.
Regular purchases remain at the core of this strategy, regardless of changes in the legislative framework. Sovereign reserves thus continue to be closely monitored by industry players.
This new progression also illustrates the stability of the acquisition mechanism adopted by the authorities. Official data allow precise tracking of the evolution of the national treasury over the weeks. The BTC thus retains a central role in this reserve strategy, which continues regularly. El Salvador therefore maintains its course, while the evolution of its holdings will continue to be observed in upcoming official updates.
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Ghiles A.
Journaliste et rédacteur web passionné par l’univers des cryptomonnaies et des technologies Web3. J’y traite les dernières tendances et actualités afin de proposer un contenu de haute qualité à un large public du secteur.
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Strategy drží 847 363 BTC v hodnotě 64,1 miliardy USD, ale BTC pod 60 000 USD uvádí firmu do ztráty a zvyšuje tlak na akcionáře i věřitele. Klíčové riziko už není likvidace, ale splatnost 1,01 miliardy USD konvertibilního dluhu 15. září 2027.
MicroStrategy’s $64 billion Bitcoin (BTC) bet has become a stress test for everyone who funded it. BTC now trades below $60,000, and the renamed company, Strategy, sits at a discount to its own holdings.
The question dividing investors is no longer whether Strategy gets liquidated tomorrow. It is who absorbs the losses while the company keeps its coins and keeps paying to hold them.
How the Bitcoin Flywheel was BuiltBy June 22, Strategy held 847,363 BTC bought for $64.1 billion, an average of $75,651 each. That is the largest corporate Bitcoin position anywhere.
MicroStrategy Bitcoin Purchases in 2026. Source: StrategyThe model runs like a flywheel. The company sells stock and debt, buys more Bitcoin, and its shares climb when BTC rises. However, falling prices spin the machine in reverse.
BTC has fallen below $60,000 this week, its lowest level since 2024. The stock has slid with it, dropping under the value of the Bitcoin on its books.
A new accounting standard made the pain visible. Since 2025, FASB rule ASU 2023-08 forces firms to mark Bitcoin to fair value each quarter. As a result, Strategy booked a $14.46 billion unrealized loss in early 2026. That produced a $12.54 billion net loss, or $38.25 for every diluted share.
Michael Saylor's Strategy currently has a $14 billion unrealized loss on bitcoin.
Tom Lee's Bitmine currently has a $10.5 billion unrealized loss on ETH.
This is why it's foolish to follow the smart money and not take profit.
They can survive a crypto winter, most of will not!
— Layah Heilpern (@LayahHeilpern) June 25, 2026 Follow us on X to get the latest news as it happens
Who Actually Pays for MicroStrategy’s Bitcoin BetThe bill does not fall on Strategy alone. As the flywheel slows, the cost spreads to five groups, in rough order of exposure.
Common shareholders They stand first in line. When the stock trades below the value of its Bitcoin, the company still raises cash by selling new shares. Each sale buys less Bitcoin than it hands away.
“If we decide to sell $1 billion of MSTR stock and buy $1 billion of Bitcoin… when you do it at 1.0x MNAV… it is dilutive. It is a minus 48 basis point yield. It costs the shareholders $310 million,” Michael Saylor, Executive Chairman, Strategy, said during Q1 2026 earnings call.
Existing owners are left holding a smaller claim on the same coins, and that dilution is how the strategy gets funded.
Investors in other treasury companies The copycats have fared worse than the original. Their shares once traded far above the Bitcoin they held, lifted by hype.
As that premium faded, many Bitcoin treasury company stocks fell much harder than Bitcoin itself, leaving late buyers deep underwater.
“If that’s not already a bubble burst, how would that bubble burst?” Tom Lee, Chairman of BitMine, said while many treasury stocks traded below net asset value.
Passive and index fund investors This group never chose the bet. MSCI has proposed removing companies whose digital assets exceed half their total assets from its global indexes.
“Feedback from the consultation confirmed institutional investor concern that some DATCOs exhibit characteristics similar to investment funds, which are not eligible for inclusion in the MSCI Indexes,” MSCI said in its official announcement earlier this year.
Strategy clears that bar with ease. An exclusion would force index funds and pension trusts to sell automatically, whatever the price, just to keep tracking the benchmark.
Convertible bondholders and preferred shareholders These investors lent on the assumption that MicroStrategy could always refinance. If Bitcoin stays depressed into 2027, that assumption breaks.
“Proceeds from the bitcoin sales are expected to be used to fund distributions on preferred stock,” Strategy indicated in the June 1 Form 8-K.
Bondholders can demand cash, and preferred holders still expect dividends, both drawing on a reserve of just $1.4 billion.
MicroStrategy itself The company is the backstop of last resort. On its first quarter 2026 earnings call, Michael Saylor again framed Strategy as a net buyer that never sells.
“We will probably sell some Bitcoin to fund a dividend just to inoculate the market, just to send the message that we did it.”
Yet if financing freezes while debt and dividends come due, keeping that vow could become impossible.
“We will sell Bitcoin when it is advantageous to the company. We are not going to sit back and just say we will never sell the Bitcoin,” Strategy co-CEO Phong Le added.
The Real Test Arrives in 2027MicroStrategy faces no margin call today. Its main debt is unsecured, so a falling price alone cannot trigger a forced sale. The threat is a date, not a level.
Holders of a $1.01 billion convertible note can demand repayment on September 15, 2027. If the shares sit below the conversion price, that claim becomes a cash bill the company must cover.
Strategy has neared this edge before. A 2022 Silvergate loan backed by Bitcoin carried a margin call near $21,000 before the firm repaid it. Moving to unsecured notes and preferred stock removed the automatic trigger, but not the obligation.
Microstrategy took a loan to buy more #bitcoin a few months ago using 19,000 $BTC as collateral.
Margin call price is $21,000…
Time to post some more collateral I think!
— Lark Davis (@LarkDavis) June 13, 2022 Some peers have already blinked. This month one Nasdaq company sold Bitcoin to repay debt, and its shares jumped. Analysts have also questioned Strategy’s exit liquidity if it is ever forced to sell at scale.
For now, no forced sale looms. The pressure has simply moved from a price trigger to a calendar. The number that matters is no longer $60,000, but the September 2027 repayment date.
Šance na schválení CLARITY Act v roce 2026 klesly na 42 %, což je pro XRP zásadní rána. Zákon by totiž zapsal jeho status digitální komodity do federálního práva.
For most of 2026, the CLARITY Act has been XRP’s one great catalyst, the bill that would write its commodity status into federal law. Now prediction markets put its 2026 passage at 42%, down from the low seventies, as a human-trafficking backlash, a banking-lobby fight, and a closing legislative window collide. Here is what the falling odds actually mean for XRP.
Summary
Prediction markets now price the CLARITY Act’s chances of becoming law in 2026 at around 42%, down sharply from highs near 73% earlier in the year. The bill would codify XRP’s classification as a digital commodity into federal statute, the catalyst analysts say could unlock billions in institutional ETF demand. The odds fell as an anti-trafficking coalition attacked a decentralized-finance provision, the banking lobby fought stablecoin rules, and the path to 60 Senate votes narrowed. The legislative window is closing fast: the White House targeted a July finish, the Senate Banking and Agriculture versions still need reconciling, and the August recess effectively ends the year’s chances. For XRP, passage could open a path toward analyst targets of several dollars, while failure or delay removes its one Ripple-specific catalyst and leaves it moving with Bitcoin. For most of 2026, XRP has had one great catalyst hanging over it, a single piece of legislation that holders have treated as the event capable of finally breaking the token out of its year-long range: the CLARITY Act, the crypto market-structure bill that would write XRP’s status as a digital commodity into federal law. For months the bill advanced, clearing the House, then a key Senate committee, and prediction markets priced its passage as increasingly likely, with odds climbing into the low seventies. That optimism has now reversed. As of late June, prediction-market data assigns roughly a 42% probability that the CLARITY Act becomes law in 2026, a sharp decline that reflects mounting trouble on several fronts at once.
A bill that looked, for a while, like it was on a glide path to the president’s desk now sits on a knife edge, and because XRP’s near-term thesis has been so tightly bound to it, the falling odds are a genuinely important development for anyone holding the token. The reason the odds matter so much is that the CLARITY Act is not just another crypto bill for XRP; it is the specific catalyst the market has been waiting on, the one event that could turn today’s favorable but fragile regulatory interpretation into durable statutory certainty. Spot XRP exchange-traded funds have launched and gathered over $1 billion, the token won legal clarity when its long battle with the securities regulator ended, and a later joint classification treated it as a digital commodity, but all of that rests on interpretive ground that a future administration could in principle reverse. The CLARITY Act would put XRP’s commodity status into actual law, removing the last layer of uncertainty that keeps large institutions on the sidelines, and analysts have projected that passage could unlock several billion dollars in additional ETF inflows.
This piece explains why the odds have fallen, the specific obstacles now in the bill’s path, the closing legislative window, and, most importantly, what each outcome, passage or failure, would actually mean for XRP’s price and prospects. The aim is to give holders a clear, grounded read on a catalyst that has become harder to handicap.
Why the odds fell The decline from the low seventies to the low forties did not come from a single event but from a convergence of problems that have collectively made passage look less certain. The most striking new obstacle is a backlash centered on a specific provision of the bill. According to a letter obtained by a Washington publication, the Alliance to End Human Trafficking, a Catholic-backed anti-trafficking organization, urged Senate leaders to revisit a decentralized-finance provision in the CLARITY Act, warning that it could weaken safeguards against illicit finance. The concern centers on Section 604 of the bill, which would codify the Blockchain Regulatory Certainty Act.
Under that provision, software developers who build decentralized blockchain applications would not be held responsible for crimes committed by users of those platforms and would not be treated as money transmitters. The anti-trafficking group warned that this language could open regulatory gaps that make it harder for authorities to detect and track financial activity tied to crimes such as human trafficking. This kind of opposition is politically potent in a way that technical crypto disputes are not, because it reframes the bill from a question of market structure into a question of whether Congress is weakening tools used to fight trafficking. That framing gives wavering lawmakers a powerful reason for caution.
It is not the only pressure. The banking lobby has been fighting provisions related to stablecoin yield and what it characterizes as insufficient bank-equivalent regulation for stablecoin issuers, with prominent banking figures vowing to challenge the bill on the floor, because the CLARITY Act’s framework directly threatens traditional finance’s competitive position in payments. Layered on top is the simple arithmetic of the Senate, where advancing major legislation requires 60 votes to overcome a filibuster. With the governing party holding 53 seats, the bill needs at least seven crossover votes from the opposition, a structurally harder problem than the committee votes it has already cleared.
Each of these pressures, the trafficking backlash, the banking fight, and the vote math, has chipped away at the perceived likelihood of passage, and together they explain why the market has repriced the odds so sharply downward. That is also why the politics around the bill now matter as much as the market-structure text itself. The policy framework may be close, but the votes still have to survive a crowded field of objections before the bill reaches the president’s desk.
The provision at the center of the fight It is worth dwelling on Section 604, because it has become the lightning rod, and understanding it clarifies why the bill suddenly looks more vulnerable. The provision would codify into law a principle that the crypto industry considers foundational: that developers who write the code for decentralized applications should not be treated as money transmitters and should not be held criminally liable for what users do with their software, in the same way that the makers of a web browser or an email protocol are not liable for crimes committed using those tools. To the industry, this is a basic protection for open-source software development, without which building decentralized systems in the U.S. becomes legally perilous. It is one of the reasons crypto firms have pushed so hard for the bill.
To critics, the same provision looks like a loophole. The anti-trafficking coalition’s argument is that by shielding decentralized-finance developers from money-transmitter obligations, the language could remove a layer of monitoring and accountability that helps authorities trace illicit funds, including money tied to human trafficking and other serious crimes. The dispute is, at its core, a genuine and difficult policy tension between two legitimate goals: protecting software developers and open innovation on one side, and preserving law-enforcement tools against financial crime on the other. That tension is precisely what makes the provision such an effective pressure point, because it cannot be dismissed as mere industry lobbying or partisan obstruction; it pits real concerns against each other.
For the bill’s prospects, the significance is that Section 604 gives opponents a substantive, morally weighted objection to rally around, and gives undecided senators a defensible reason to demand changes or withhold support. That is exactly the kind of friction that can stall legislation when the calendar is tight and the vote margin is thin. The bill does not only need supporters who like digital-asset clarity; it needs senators who are comfortable defending the developer-shield language under pressure from law-enforcement and anti-trafficking groups. That is a harder political task than simply explaining why tokens need a market-structure framework.
The legislative window is closing Even setting aside the substantive fights, the CLARITY Act faces a brutal constraint that may matter more than any single objection: time. The legislative calendar for passing a controversial bill in 2026 is narrow and closing. The White House pushed for a finish around the July 4 holiday, a target that officials themselves conceded was tight, and the harder deadline is the August recess, after which campaigning for the autumn elections begins in earnest and the Senate’s floor schedule effectively closes to contested votes. Any realistic path to passage this year therefore runs through a small number of remaining legislative days, and every additional dispute consumes some of that dwindling supply.
Compounding the time pressure is a procedural step that the headline timeline often obscures: reconciliation between two Senate committees. The CLARITY Act’s framework splits jurisdiction over digital assets between the securities regulator and the commodities regulator, and because both the Senate Banking Committee and the Senate Agriculture Committee have claimed a stake, the Banking Committee’s version of the bill must be merged with the Agriculture Committee’s companion legislation before any floor vote can happen. That merger is not complete. The bill cleared the Banking Committee on a bipartisan vote in May and was placed on the Senate’s legislative calendar in early June, making it formally eligible for floor consideration, which is the closest it has ever been to becoming law.
But floor eligibility is not passage. To actually become law, the bill must still be reconciled across the two committees, survive a 60-vote floor vote, be reconciled again with the version the House passed, and then be signed by the president. Each of those steps takes time the calendar may not provide, and if the vote does not come before the recess, the political window that opened this opportunity may not reopen on the same terms. One senator who has championed the bill captured the stakes bluntly, saying they did not come this far to quit at the five-yard line, but the five-yard line in a closing window is exactly where bills die.
What passage would mean for XRP For XRP holders, the entire point of tracking the CLARITY Act is what its outcome would do to the token, so it is worth being specific about both scenarios, beginning with passage. If the bill becomes law and codifies XRP’s digital-commodity status into federal statute, the most important effect would be the removal of the last meaningful layer of regulatory uncertainty, which is the gatekeeper that has kept large institutions cautious. XRP already enjoys more regulatory clarity than almost any major token after its legal battle ended and the joint classification treated it as a commodity, but that clarity rests on interpretive releases rather than statute, and a statute is far more durable. With permanent legal footing, the institutional capital that has waited on the sidelines, pension funds, asset managers, and the like, would have the certainty it needs to allocate.
The clearest channel for that capital is the spot ETF complex. Analysts at a major bank have projected that passage and the resulting clarity could drive several billion dollars of additional inflows into XRP exchange-traded funds, on the order of three to six times what those funds have gathered since launching. Flows of that magnitude would represent a demand shock large enough to push XRP through the resistance levels that have capped it and toward higher targets, with mainstream analyst forecasts in a passage scenario clustering in the several-dollar range by year-end. The more bullish projections reach higher still if a second catalyst, such as Ripple securing a Federal Reserve master account, were to follow.
The important caveat is that some of this may already be partly priced in, because the market has watched the bill advance for months, so the real question is not whether clarity helps XRP but how much of the waiting money actually moves once passage is law versus how much already has. Still, the directional case is clear: passage would be a powerful, fundamentally positive catalyst for XRP, the event that could finally connect the token’s long-promised institutional thesis to actual demand. It would also sit alongside another XRP catalyst in the spotlight, where holders have been trying to separate company-level events from token-level value. In this case, unlike many Ripple corporate developments, the statutory classification would apply directly to the token.
What failure or delay would mean The other side of the ledger is just as consequential, and with the odds now below even, it deserves equal weight. If the CLARITY Act fails or stalls, whether by missing the legislative window, dying in the reconciliation process, or falling short of 60 votes on the floor, XRP would lose its one Ripple-specific catalyst, the single event distinguishing it from the rest of the market. In that scenario, XRP would likely revert to moving with Bitcoin rather than leading on its own regulatory story, surrendering the independent upside that the bill represented. The institutional flows that have supported XRP could reverse, the way weekly ETF inflows did earlier in the year when momentum faded, falling from over $200 million to a trickle within a month.
Without the statutory catalyst, Ripple’s institutional infrastructure would keep growing through stablecoins and fiat rails, but in a way that does not necessarily drive XRP token demand, leaving the familiar gap between corporate progress and token price intact. That is XRP’s other open question: whether Ripple’s wins translate into XRP demand, or whether stablecoins and company-level infrastructure capture most of the value. If the CLARITY Act fails, that question becomes even more important because the regulatory unlock would no longer be there to carry the near-term thesis. XRP would then need ETF flows, ledger usage, and broader crypto risk appetite to do the work instead.
The price implications of failure are meaningful. Analysts have suggested that in a no-bill scenario, XRP could slip back toward the lower end of its range, with some pointing to support around the $1.20 to $1.30 area and warning that a break of the key technical floor on a broader market sell-off could open a path toward materially lower levels with little support in between. A bank that projected large inflows on passage had already trimmed its XRP target on the assumption of a delayed bill rather than a failed one, illustrating how much of the token’s valuation has been riding on this single legislative outcome. That is why the price levels at stake matter: the legal catalyst and the technical chart are now feeding into each other.
The sharpest risk is not merely that the bill fails this year but that failure pushes it out of reach entirely, since a missed 2026 window could shelve the effort for years if the political configuration that enabled it does not recur. For XRP, that would mean losing not just a near-term catalyst but the central pillar of its independent investment case, throwing the token back onto Bitcoin’s coattails and onto the slow, uncertain process of turning network usage into token demand without the regulatory unlock.
The priced-in problem A subtler issue complicates both scenarios and deserves its own attention, because it shapes how XRP might actually react to news: the question of how much of the CLARITY Act’s effect is already in the price. Markets are forward-looking, and the bill’s advance has been the most-watched regulatory story in crypto for the better part of a year, which means XRP’s current price already embeds some probability of passage. This creates a genuine puzzle for holders. If passage is partly priced in, then the actual event, should it come, might produce a smaller pop than the headline suggests, as the market has already bought the rumor and could sell the news.
Conversely, if the market has grown skeptical and priced the bill closer to the current 42% odds, then a clear passage could still surprise to the upside by forcing a repricing toward certainty. This is why XRP has traded in a range even as the bill progressed: each catalyst has been priced as a possibility instead of a fact, because a proof-of-concept settlement is priced as a proof of concept until it becomes recurring volume, an ETF is priced on the flows it actually attracts instead of the flows it might, and a legislative catalyst is priced on the probability of passage, which for the CLARITY Act has stayed well short of certainty. A token sitting on a stack of maybes trades like a token sitting on a stack of maybes: range-bound, reactive, and quick to sell the news. That is the practical problem facing XRP now.
The practical implication for holders is that the falling odds are informative in two directions. They lower the probability the market assigns to the positive catalyst, which is bearish, but they also mean that less of the good news is now priced in, which paradoxically increases the potential upside surprise if the bill does pass against the odds. The cleanest way to read XRP right now is as a token whose price reflects a market that has grown genuinely uncertain about its central catalyst. That makes both the downside of failure and the upside of surprise passage larger than they would be if the outcome were close to settled.
What holders should watch For an XRP holder trying to navigate a catalyst that has become harder to handicap, the analysis points to a focused set of signals worth tracking over the coming weeks. The first and most important is simply whether a floor vote gets scheduled before the August recess, because the closing window is the binding constraint, and the absence of a scheduled vote as the recess approaches would be a strong signal that 2026 passage is slipping away. The progress of the committee reconciliation between the Banking and Agriculture versions is a related early indicator, since the floor vote cannot happen until that merger is done. The second signal is the trajectory of the opposition, particularly whether the Section 604 trafficking objection gains traction with undecided senators or whether sponsors find a way to address it, because that fight has the potential to either stall the bill or, if resolved, clear a path.
The third thing to watch is the prediction-market odds themselves, which have proven to be a useful real-time gauge of the bill’s perceived chances and which will move as developments unfold; a recovery back toward the sixties or seventies would signal renewed momentum, while a further slide would confirm the pessimism. Alongside the legislative signals, holders should keep an eye on the observable market data that will register the outcome regardless of the politics: ETF flows, which would surge on passage and stall on failure, and XRP’s behavior around its key technical levels, particularly whether it holds the support that the bear case threatens. The stablecoin fight also matters because it is one of the pressure points inside the bill, and the stablecoin rules in the bill are part of why banks and crypto firms are fighting so hard over the final text.
The honest synthesis is that the CLARITY Act has gone from a likely catalyst to a genuine coin flip, and with it XRP’s near-term path has become a binary bet on a contested vote in a closing window. Passage would be a powerful positive catalyst capable of unlocking institutional demand; failure would strip XRP of its defining catalyst and throw it back onto Bitcoin’s movements. At 42% and falling, the market is telling holders that the outcome it once treated as probable is now anything but. The next few weeks of the legislative calendar are likely to decide which way XRP breaks.
Frequently asked questions What is the CLARITY Act and why does it matter for XRP? The CLARITY Act is a crypto market-structure bill that would codify the classification of tokens like XRP as digital commodities into federal law. For XRP, this matters enormously because the token’s current commodity status rests on interpretive regulatory releases instead of statute, which a future administration could in principle reverse. Writing that status into actual law would remove the last major source of regulatory uncertainty that keeps large institutions cautious, and analysts have projected that passage could unlock several billion dollars in additional XRP ETF inflows. It has been XRP’s single most important catalyst throughout 2026, which is why its odds of passing move the token.
Why did the CLARITY Act’s odds fall to 42%? The odds fell from highs near 73% because of several problems converging at once. An anti-trafficking coalition attacked Section 604 of the bill, a provision shielding decentralized-finance developers from money-transmitter obligations, warning it could weaken tools against illicit finance. The banking lobby has fought provisions on stablecoin yield and regulation, while the Senate math is hard because advancing the bill requires 60 votes, meaning at least seven crossover votes from the opposition. Combined with a closing legislative calendar, these pressures made passage look far less certain, and prediction markets repriced the probability sharply downward to around 42%.
What happens to XRP if the CLARITY Act passes? Passage would remove the last layer of regulatory uncertainty by writing XRP’s commodity status into durable federal law, giving cautious institutions the certainty they need to allocate. The clearest effect would flow through spot ETFs, with analysts projecting several billion dollars of additional inflows, three to six times what the funds have gathered so far. That demand could push XRP through its resistance levels toward analyst targets in the several-dollar range by year-end, with higher projections if a second catalyst like a Federal Reserve master account followed. The main caveat is that some of this may already be priced in, so the size of the reaction depends on how much waiting money actually moves.
What happens to XRP if the bill fails? Failure or delay would strip XRP of its one Ripple-specific catalyst, likely sending it back to moving with Bitcoin instead of leading on its own regulatory story. Institutional ETF flows could reverse, as they did earlier in the year when momentum faded, and analysts have suggested XRP could slip toward support around $1.20 to $1.30, with a break of its key floor on a broader sell-off opening a path to materially lower levels. The sharpest risk is that a missed 2026 window could shelve the effort for years. That would cost XRP not just a near-term catalyst but the central pillar of its independent investment case.
When is the deadline for the CLARITY Act? The practical deadline is the Senate’s August recess, after which election-year campaigning effectively closes the floor schedule to contested votes. The White House had pushed for a finish around the July 4 holiday, a target officials conceded was tight. Before any floor vote, the Senate Banking Committee’s version must be reconciled with the Senate Agriculture Committee’s companion bill, a merger that is not yet complete, and after a floor vote the bill would still need to be reconciled with the House-passed version and signed by the president. If the vote does not happen before the recess, 2026 passage becomes very unlikely.
Is the CLARITY Act’s effect already priced into XRP? Partly, which complicates how the token may react. The bill’s advance has been the most-watched regulatory story in crypto for nearly a year, so XRP’s price already embeds some probability of passage, which is part of why the token has stayed range-bound: each catalyst gets priced as a possibility instead of a fact. If passage is partly priced in, the actual event could produce a smaller move than expected. But with odds now down at 42%, less of the good news is currently priced in, which paradoxically increases the potential upside surprise if the bill passes against the odds, while also reflecting greater downside risk if it fails.
This article is information, not investment advice. Legislative timelines, prediction-market odds, prices, and analyst projections reflect reporting available as of June 28, 2026, and can change quickly. The status and prospects of the CLARITY Act are uncertain and contested. Nothing here is a recommendation to buy or sell XRP or any security. Verify current developments from primary sources and consider your own circumstances before making any decision.
California’s DFAL Clock Is Ticking: XRP Price Hanging in the Balance
Ahmed Barakat
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Ahmed Balaha is a journalist and copywriter based in Georgia with a growing focus on blockchain technology, DeFi, AI, privacy, digital assets, and fintech innovation.
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California’s Digital Financial Assets Law will take effect on July 1. It requires any firm conducting digital asset business activity with state residents to hold a DFAL license, and have a completed application on file with the DFPI, or cease covered operations. Right now, as of public records, no Ripple entity appears among applicants. XRP price has fallen below the $1.10 level at this moment of uncertainty.
DFAL covers the exchange of digital assets for fiat or other digital assets, their transfer between persons, custody, and the issuance of reserve-backed instruments. It maps directly onto Ripple’s California-facing operations: payments infrastructure, custody services, and the issuance and redemption of RLUSD, Ripple’s dollar-pegged stablecoin.
Ripple’s existing portfolio of 40-plus U.S. money transmitter licenses does not automatically satisfy DFAL; the law is a separate regime administered by the DFPI through the Nationwide Multistate Licensing System.
However, there are three paths to legal compliance by July 1: hold a DFAL license, have a completed application pending with the DFPI, or qualify under a narrow statutory exemption, primarily available to banks, certain trust companies, and SEC- or CFTC-registered entities operating within already-regulated activity.
🗓️Key date for @Ripple – July 1.
Ripple previously engaged CA's DFPI for a DFAL license noting firms can keep operating if submit by 7/1/26. Public docs through March '26 don't list any Ripple entities, though likely filed. Necessary for all CA offerings, issue/redeem/custody. pic.twitter.com/xfQK4Z3IBc
— WrathofKahneman (@WKahneman) June 19, 2026 Ripple has engaged with the process as the company submitted a formal comment letter to the DFPI, pushing to eliminate redundant money transmitter license requirements for DFAL-licensed firms. However, engagement is not the same as a filed application.
Law firms, including Chambers-ranked practices, have described DFAL as one of the most expansive state-level digital asset licensing regimes in the country.
Discover: The Best Crypto to Diversify Your Portfolio
Can XRP Price Hold $1 If Ripple Misses the DFAL Deadline?XRP is trading near $1.10, far below the expected $2.50 many predicted. Recent price action reflects weak momentum, with sellers repeatedly capping rallies around the $1.15 to $1.20 area. Despite ongoing attention on Ripple’s regulatory developments, the market has yet to price in a decisive positive outcome.
Meanwhile, investors remain focused on several legal and regulatory milestones involving Ripple. The court’s earlier finding that XRP itself is not inherently a security removed a major uncertainty. However, the remaining penalty and injunction issues still matter because they could influence Ripple’s future business operations and market sentiment.
From a technical perspective, XRP must first reclaim the $1.15 to $1.20 zone before traders can discuss a stronger trend reversal. If buyers regain control and regulatory developments remain favorable, the next resistance area could emerge around $1.30 to $1.50. A sustained move above those levels would likely require a meaningful catalyst.
On the downside, support remains clustered around $1.05 and $1.00. If regulatory expectations weaken or broader crypto markets turn lower, those levels could come under pressure. The $1.00 mark remains an important psychological threshold, as a decisive break could invite additional selling.
For now, the market appears to be waiting for confirmation rather than trading on assumptions. Regulatory progress could improve sentiment, yet XRP’s longer-term trajectory will likely depend on both legal clarity and stronger demand returning to the market.
Don’t Miss Out on Our $1,000 USDT Airdrop on ByBit
XRP prošel masivní likvidací longů za 6,7 mil. USD, zatímco open interest klesl o 11 %. Držitelé na spotovém trhu zůstali klidní a denní aktivní adresy za dva týdny vzrostly o 71,7 %.
28 June 2026 | 15:41 The story in XRP is a split screen: the derivatives market just went through a violent, one-sided purge of leveraged bets, while network usage keeps climbing.
Key Takeaways XRP saw a one-sided long-liquidation flush, peaking at $6.7M on June 22. Open interest fell 11%, meaning purged positions aren’t being rebuilt. Active addresses rose almost 72% in two weeks even as price fell. XRP trades for $1.04 at the time of writing. The recent move was driven by a liquidation cascade: an 830% spike in long liquidations, which is a mechanical event rather than a sentiment reading. Margin thresholds were breached and positions were force-closed automatically. The roughly $3M in long liquidations dwarfing the short side confirms how one-sided it was, this was a purge of upside bets, not a balanced deleveraging. The climax came on June 22 with a $6.7M flush, the single largest burst of forced selling on the chart, landing exactly as price hit its lowest point near the $1.05 range.
What happened next matters as much as the flush itself. According to recent report, shared by CryptoQuant, open interest dropped from $1.18B to $1.04B, down 11%, while this played out. That’s the tell that separates a flush from a rotation: positions are being closed and not rebuilt. Traders aren’t re-entering, which leaves the market structurally lighter and less amplified than before.
The Funding Rate Hit Its Floor The funding rate adds the second layer. It reached its deepest negative reading of the entire March-to-June window right at the June 22 climax, a -463% shift against the quarterly baseline. Negative funding means shorts are the dominant paid position, longs are effectively being compensated just to hold their positions open.
This is where precision matters. At extremes, negative funding is mechanically unsustainable, because shorts eventually have to cover, which can create upward price pressure. But that’s a precondition for a squeeze, not a guarantee of one, and it should not be read as bullish on its own. It describes a compressed setup, a spring under tension, without saying anything about whether or when it releases.
The Split That Defines Who Actually Sold Here’s the most analytically important data point in the whole picture. While the futures market cascaded, Binance spot reserves fell just 0.35% on the week. Spot holders, in other words, didn’t panic-sell onto exchanges. That cleanly separates two very different actor types: leveraged speculators, who got wrecked, and spot holders, who barely moved.
The absence of spot capitulation during a violent futures flush is what tells you the nature of the selling. This was derivatives-manufactured, the forced unwinding of leveraged positions, rather than organic distribution by the people who actually hold XRP. That distinction changes how to read the entire episode: it was a leverage problem, not a conviction problem among holders.
Metric Status/Result Significance Long Liquidations $6.7M peak (June 22) Violent, one-sided flush of leveraged bets. Open Interest Down 11% Positions are closed, not rebuilt; market is lighter. Binance Spot Reserves Down 0.35% Spot holders didn’t panic; selling was derivatives-manufactured. Active Addresses +71.7% (2 weeks) Real engagement diverging from speculative price drops. The Network Is Growing as Price Falls Now the counter-signal. Daily active addresses rose from about 23,000 on June 14 to nearly 39,500 by June 27, a 71.7% increase in two weeks, according to Ali Charts citing Santiment. Price fell over roughly the same window. Network usage expanding while price contracts is a genuine divergence, and historically these kinds of divergences don’t tend to persist indefinitely.
Network activity on $XRP has surged over the past two weeks.
Daily active addresses have climbed from 23,000 on June 14 to nearly 39,500 today, signaling growing on-chain participation. pic.twitter.com/lqX9oo3AsS
— Ali Charts (@alicharts) June 28, 2026
It’s important to be exact about what this does and doesn’t say. It doesn’t predict direction. What it indicates is that the chain is being used more, not abandoned, real engagement separating from speculative price behavior. Set against the derivatives picture, the contrast is stark: the futures market shows panic, while the network shows growth.
The Setup, and What Could Confirm a Direction Put the layers together and what you have is structural cleanup, not a directional call. The leverage has been flushed, open interest has compressed and isn’t rebuilding, funding sits at an extreme, spot holders stayed put, and on-chain activity is rising. That combination describes a market that’s been deleveraged and is being actively used, which could resolve in either direction.
The honest framing is that the network’s continued growth provides a floor narrative, evidence the chain isn’t being abandoned, rather than a price prediction. As for what to watch: the negative funding extreme is the squeeze precondition, but the signal that would actually confirm a direction is open interest. If OI starts rebuilding alongside rising price, that’s leverage returning on the long side; if it stays compressed, the market remains light and unconfirmed either way. The deleveraging is real and largely complete.
This article is for informational purposes only and does not constitute financial advice. Consult a professional before making investment decisions.
Author
Kosta has reported on cryptocurrency markets and blockchain infrastructure since 2020, bringing over six years of hands-on experience in the crypto industry built through daily tracking of markets, trends, and emerging blockchain developments. Specializing in Bitcoin on-chain analysis, institutional ETF flows, and digital asset price action, his work at Coindoo has been cited by other news agencies and consistently covers market developments with a focus on data-driven reporting across Bitcoin, Ethereum, Solana, and XRP. Over the years, Kosta has contributed to multiple crypto media outlets in different regions, authoring over 6,000 articles across the sector. His reporting spans cryptocurrency markets and the broader fintech industry, tracking not only price action but also the technological and regulatory forces shaping the ecosystem. To support his analysis, Kosta actively leverages on-chain data and metrics from leading platforms such as Santiment, Glassnode, and CryptoQuant, enabling deeper, evidence-based market insights. He believes in the power of transparency and the data that underpins the blockchain ecosystem. His academic background in Marketing Management from Denmark further complements his analytical approach, adding a strong understanding of communication strategy and content positioning to his work.
Brad Garlinghouse řekl, že Ripple by po případném IPO mohl pro držitele XRP udělat „něco speciálního“, ale ne v dohledné době. Nepotvrdil žádný konkrétní mechanismus ani žádný slib.
Brad Garlinghouse said one word, “maybe,” and the XRP community heard a promise. Asked whether holders could get a piece of Ripple if it goes public, he nodded toward a “special arrangement.” This is what was actually said, what holders could realistically receive, and the downside almost nobody is talking about.
Summary
Ripple chief executive Brad Garlinghouse said that “if and when” Ripple goes public, the company might do “something special” for XRP holders, then immediately added it was “not in the immediate term.” That hedged “maybe” was offered in response to a direct question, not volunteered as a plan, and he declined to commit to any mechanism such as a token buyback. Ripple and XRP are legally and financially separate assets: holding XRP grants no shares, no dividends, and no claim on Ripple’s corporate profits, and no bridge between the two currently exists. The mechanisms holders imagine, preferential IPO share access, long-term holding rewards, or tokenized Ripple equity, are all unannounced and face serious securities-law hurdles given XRP’s legal history. The overlooked risk is that a Ripple IPO could actually pressure XRP, by drawing institutional capital toward Ripple stock and pushing the company to monetize its escrow holdings to satisfy public-market investors. One word from Ripple’s chief executive set the XRP community alight, and that word was “maybe.” Speaking on the “Crypto In America” podcast with journalist Eleanor Terrett, Brad Garlinghouse was asked the question XRP holders have wanted answered for years: if Ripple ever goes public, could the people who hold XRP get a piece of it. He did not say no. He gestured first at the indirect benefits Ripple already provides, then, pressed on whether the company would do something specific for holders in an initial public offering, he said, “Maybe, but that is not in the immediate term.”
JUST IN: Ripple CEO Brad Garlinghouse says the company processed $13T in payments last year with no immediate IPO plans pic.twitter.com/f9bd80FPsX
— crypto.news (@cryptodotnews) May 5, 2026 That was the entire substance of it, a hedged possibility wrapped in a qualification, offered in answer to a direct question rather than announced as a plan. And yet within hours it had been clipped, shared, and reshaped across XRP social media into something close to a corporate commitment, with community members urging one another to “hold accordingly.” The gap between what Garlinghouse actually said and what the community heard is the real story here, because the difference between a hinted-at maybe and a planned reward is the difference between a reasonable hope and a misplaced expectation.
The reason the remark landed so hard is the situation it landed into. XRP holders have spent 2026 watching Ripple collect exactly the kind of institutional wins the community long predicted, settlements with JPMorgan, stablecoin launches with major partners, a steady drumbeat of bank deals, while the token itself has stayed pinned near a dollar and change, beneath every major moving average. That combination, corporate triumph paired with token stagnation, breeds a particular hunger: the sense that the wins are real but are somehow not reaching holders, and that some missing mechanism could finally connect the two. Into that hunger dropped Garlinghouse’s nod, and it did what a catalyst does in a starved market.
This piece separates the hope from the reality. It covers exactly what was said and the precise wording that matters, the crucial distinction between Ripple the company and XRP the token, the mechanisms a holder benefit could theoretically take and why each is harder than it sounds, why Ripple may not even go public soon, the indirect benefit Ripple genuinely does provide, and the downside almost nobody is discussing: that an IPO could actually work against XRP. The goal is the real picture, neither dismissing the possibility nor inflating it into the certainty the hype implied.
What Garlinghouse actually said Precision matters here, because the entire community reaction rests on a few carefully chosen words, and those words were more conditional than the excitement suggested. Garlinghouse did not volunteer the remark; he was asked directly whether XRP holders could share in Ripple’s success if the company eventually launched an initial public offering. His first instinct was to point to the indirect benefit Ripple already provides, saying he hopes XRP holders feel they benefit from Ripple’s existence through the work the company does to grow the XRP ecosystem. Only when pressed on whether Ripple would do something specific for holders in an IPO scenario did he offer the line that ignited everything: “Maybe, but that is not in the immediate term.”
When pushed further on concrete mechanisms, including a possible token buyback, he declined to commit to any of them, pointing back instead to what Ripple already does for the ecosystem. So the full extent of the supposed promise is a “maybe,” qualified as not near-term, given in response to a direct question rather than offered as a plan, with no program described, no mechanism named, and no action committed to. The community heard “Ripple will do something special for holders.” What Garlinghouse actually said was closer to “maybe someday, if we go public, which is not happening soon.”
Those are not the same statement, and stacking the two conditionals reveals how far the exciting headline sits from anything concrete: a possible benefit, attached to a possible IPO, that he himself describes as not a priority. It is worth adding that days earlier, at an industry conference, Garlinghouse had been cooler still on the idea of going public at all, emphasizing that staying private gives Ripple flexibility. Read in that context, the podcast remark was a hint, not a plan and certainly not a promise. Any honest assessment of what holders would actually get has to begin from that fact rather than from the amplified version that spread online.
Ripple is not XRP: the distinction that decides everything To understand why this question is so charged, and so easily misunderstood, you have to grasp a distinction that still confuses many people: Ripple and XRP are legally and financially separate assets, and owning one does not mean owning the other. Ripple is a private technology company that builds payment and liquidity products, some of which use the XRP Ledger. XRP is a cryptocurrency, the native asset of the XRP Ledger, which is a decentralized, open-source blockchain that Ripple does not control. Holding XRP gives you ownership of that token and nothing else.
It confers no shares in Ripple, no dividends, no voting rights, and no claim whatsoever on Ripple’s corporate profits or assets. The two are different things with different value drivers, and the price of one does not automatically move the other. That distinction is why the company-versus-token gap keeps resurfacing across Ripple’s 2026 story. Ripple can win institutional business, launch products, and deepen its corporate value without automatically delivering a direct benefit to XRP holders.
This separation is the foundation of the entire holder-payout question, because it means there is no existing structure, no dividend, no buyback mechanism, no holder-equity bridge, that currently connects Ripple’s corporate fortunes to the people who hold XRP. Any such benefit would require a deliberate corporate decision: Ripple choosing to extend something to holders of a token that is legally distinct from its stock. That is precisely what makes Garlinghouse’s “maybe” notable, because it gestures at the possibility of Ripple voluntarily building a connection that does not exist and is not required to exist. The community’s hope is that Ripple might someday decide to construct that bridge.
The reality is that no bridge exists today, none is planned, and the entire question is whether Ripple might ever choose to build one. Everything that follows, every imagined mechanism and every obstacle, flows from this single fact: a Ripple IPO would, by default, do nothing for XRP holders, because the token and the company are separate. Only an affirmative, deliberate choice by Ripple could change that. Until such a choice is announced, a holder payout remains speculation, not entitlement.
The mechanisms holders imagine Once the “maybe” spread, the community began filling in the blank with specific mechanisms, and it is worth laying them out, because they define the range of what “something special” could plausibly mean. The most discussed idea is preferential access to IPO shares, an arrangement in which verified long-term XRP holders, or users staking on the XRP Ledger, would be granted priority subscription rights to buy into a Ripple offering at favorable terms before the general public. This is the version that most directly answers the community’s wish, because it would let XRP holders transition, at least partly, into Ripple shareholders. It would turn token loyalty into an equity stake.
A second imagined mechanism is a long-term holding reward, a community-based structure that would give some benefit to holders who have kept XRP for a defined period, rewarding loyalty without necessarily handing over equity. A third, more technically ambitious idea is tokenized Ripple equity: a blockchain-based representation of Ripple stock made available to eligible token holders, which would use the very tokenization technology the industry is racing to build in order to bridge the gap between Ripple shares and XRP. Some in the community have also floated the notion of an “equity-token-bound” proof of entitlement, a digital claim linking XRP holding to some future right in Ripple. Each of these would, in its own way, construct the bridge between Ripple equity and XRP holders that currently does not exist.
The crucial thing to hold in mind is that all of them remain imagined, not announced. Garlinghouse named none of them; he declined, in fact, to endorse any specific structure when asked. They represent the community’s wish list of what “something special” might be, not a menu Ripple has offered. The distance between a fan’s plausible idea and a company’s actual program is considerable, especially when the imagined benefit touches securities law, global compliance, investor eligibility, and the legal separation between Ripple equity and XRP.
Why each mechanism is harder than it sounds The reason Garlinghouse spoke in hints instead of specifics is almost certainly that nearly every concrete version of a holder benefit collides with serious obstacles, and understanding those obstacles is essential to a realistic view. The largest is securities law, and it is a particularly sharp problem for XRP of all tokens. Linking a cryptocurrency’s holding to equity benefits raises exactly the kind of securities-law questions that defined Ripple’s long and costly legal battle, the years-long fight over whether XRP sales amounted to unregistered securities transactions. Building a formal bridge that rewards XRP holders with equity or equity-like rights risks recreating the very entanglement between the token and the company that Ripple spent years and enormous legal resources trying to separate.
The company would have to navigate that terrain with extreme care, because a poorly designed holder-benefit program could reintroduce the argument that XRP is a security tied to Ripple’s enterprise, which is the last thing Ripple wants. That is why the catalyst that matters more than the IPO is still statutory clarity from the CLARITY Act, not an undefined corporate reward. Federal clarity can strengthen XRP’s status without blurring the line between the token and Ripple equity. A holder-equity program, by contrast, could blur that line if designed carelessly.
Beyond securities law, the practical obstacles multiply. A preferential-share program would require verifying who is a genuine long-term holder, drawing cutoff lines that would inevitably be seen as arbitrary or unfair, and managing the identity and compliance machinery to do it at scale across a global, pseudonymous holder base. A holding-reward structure raises questions of how to fund it and how to avoid favoring large holders over small ones. Tokenized equity would face the full weight of securities regulation governing who can own and trade company stock, plus the technical and legal work of making a regulated equity instrument function on a blockchain.
Each mechanism, in other words, is not just a matter of Ripple deciding to be generous; it is a tangle of legal exposure, fairness problems, and operational complexity, any one of which could sink it. This is why the most dramatic interpretations of “special arrangement” are also the least likely. A sober reading has to weight the modest possibilities, a governance gesture, a symbolic recognition, or simply Ripple structuring its business so more value flows through XRP over time, far more heavily than the windfall the community imagined.
Why Ripple may not even go public soon The entire holder-benefit scenario is downstream of a prior question that often gets lost in the excitement: will Ripple even go public at all, and if so, when. On this, Garlinghouse has been consistent and notably unenthusiastic. He has repeatedly described an IPO as not a priority, and his reasoning is grounded in the current state of the public markets for crypto companies. He has pointed to the underwhelming performance of crypto-related public listings, citing peers whose post-listing stock has struggled, and noted reports that at least one major exchange had delayed its own listing plans.
His view, in short, is that the public markets have not treated Ripple’s peers well, and that there is little reason to rush into that environment. He has also made a positive case for staying private, arguing that it preserves flexibility, including, he joked, the freedom to speak openly without lawyers drafting every word. This is not the posture of a company on the verge of ringing the opening bell. It means the holder-benefit question is built on a foundation that is itself uncertain: a possible reward contingent on an IPO that the chief executive describes as neither planned nor imminent.
That is the sense in which the whole thing is a maybe attached to a maybe. For an XRP holder weighing what they might receive, this is the most important practical point, because even the most generous imaginable holder benefit is irrelevant unless and until Ripple actually decides to go public. By Garlinghouse’s own account, that decision is not on the calendar. The community’s hope therefore rests on two sequential uncertainties: first that Ripple goes public, and second that, having done so, it chooses to extend something to holders it is under no obligation to help.
Either link breaking is enough to make the whole scenario evaporate. That is why the IPO hint should not be treated like a near-term catalyst, even if it tells holders something about how Ripple thinks about its community. The comment matters as a signal of openness, but it does not change the current legal structure, the current IPO timeline, or the current token economics. XRP holders should separate those categories carefully.
The indirect benefit Ripple already provides Set against the speculation is Garlinghouse’s actual, stated position, which deserves a fair hearing because it is not a trivial argument: that XRP holders already benefit from Ripple’s existence, indirectly but intentionally. The foundation of this argument is a simple fact: Ripple is the largest single holder of XRP. That gives the company a stronger economic incentive than anyone else to increase the token’s value and adoption, because Ripple profits when XRP rises, just as holders do. Its incentives are genuinely aligned with holders, even without any formal program linking the two.
Every commercial partnership Ripple pursues, every payment corridor it opens, every institutional deal it closes, and every regulatory battle it fights is evaluated, at least in part, through the lens of how it drives XRP utility and liquidity. Garlinghouse’s framing is that this alignment is the real benefit, that Ripple’s entire strategy is built around making XRP the most useful, liquid, and trusted digital asset in payments and settlement, and that by growing the ecosystem it makes what holders own more valuable, even without a dividend or an equity link. That is where XRP’s actual utility remains central to the long-term case. The token’s real thesis has to rest on usage, liquidity, and settlement demand, not on implied ownership of Ripple.
NEW: JPMorgan, Mastercard, Ondo Finance and Ripple complete tokenized Treasury redemption test on XRP Ledger. Settlement took roughly 5 seconds compared to 3 to 5 business days on traditional rails pic.twitter.com/9Rkd3MkWF4
— crypto.news (@cryptodotnews) June 12, 2026 Garlinghouse has pointed to concrete examples of this posture, including Ripple’s backing of XRP treasury companies such as Evernorth, which is working to build a large XRP treasury business with Ripple’s support, an effort Garlinghouse frames as helping XRP holders, the XRP community, and Ripple shareholders at the same time. This argument has genuine merit and should not be dismissed as spin. The company’s commercial work plausibly does increase XRP’s utility and demand over time, which is a real, if diffuse, benefit to anyone holding the token. The counterpoint, and the reason the “maybe” resonated, is that many in the community find this indirect alignment insufficient.
They want a concrete share of Ripple’s corporate success, not an incentive structure that may or may not translate into token-price appreciation. That dissatisfaction is precisely the nerve Garlinghouse’s remark touched. His indirect-benefit argument is, in effect, his answer to it: you already benefit, just not in the direct way you want. Whether that answer satisfies holders depends on whether Ripple’s wins eventually become visible in XRP demand rather than simply in Ripple’s corporate valuation.
The downside nobody mentions: an IPO could hurt XRP Here is the part of the story that the bullish excitement almost entirely skips: a Ripple IPO is not unambiguously good for XRP, and there is a credible case that it could actively work against the token, at least in the near term. The first channel is competition for capital. Today, an institution that wants exposure to Ripple’s success has essentially one liquid way to get it: buy XRP, the token associated with the company’s ecosystem. If Ripple goes public, that changes.
Suddenly there is a direct way to own a piece of Ripple itself, a regulated equity that offers what a token cannot: potential dividends, audited financial transparency, ownership of the company’s actual assets and cash flows, and the compliance comfort of a listed stock. Faced with that choice, institutional capital that might have flowed into XRP as a proxy for Ripple could instead flow into Ripple stock, siphoning off the very institutional demand the XRP bull case depends on. The IPO, in this reading, would give the market a cleaner instrument for the Ripple thesis, and XRP could lose its role as the default vehicle for it. That is the uncomfortable side of where XRP trades while holders wait: the market wants direct token demand, not merely a story about Ripple’s corporate success.
The second channel is selling pressure from Ripple itself. As a private company, Ripple has long been criticized for selling XRP from its large escrow holdings, a persistent source of new supply. After an IPO, that pressure could intensify instead of ease, because a public company answers to Wall Street’s quarterly demands for cash flow and profitability. To satisfy those demands and bolster its financial reports, Ripple’s board could face strong incentives to monetize tens of billions of XRP from its escrow accounts in a more systematic and aggressive way, creating an invisible, long-term overhang on the token’s price.
None of this is certain, and a well-managed IPO could be handled in ways that limit these effects, but the point is that the community’s framing of an IPO as pure upside for holders is incomplete. The honest version acknowledges that going public is a double-edged sword for XRP. It could, in the bullish case, come bundled with a “special arrangement” that rewards holders, or it could, in the bearish case, drain attention and capital away from the token while increasing the supply pressure on it. Holders hoping for the first should at least weigh the second.
What it means for holders today So what should an XRP holder actually take from all of this, standing in the present with the token trading near a dollar and the “special arrangement” still nothing more than a hedged remark? The disciplined answer is to give the IPO hint the weight it actually carries, which is to say very little, and to keep attention on the catalysts that truly move XRP. A possible IPO reward is a weak basis for any decision, because it is a maybe attached to a maybe: an unplanned, undefined benefit contingent on an IPO that Ripple does not prioritize. It is better regarded as a distant possible upside not to be counted on than as a catalyst to position around.
The things that will actually determine XRP’s path are observable and concrete: whether the CLARITY Act passes and writes XRP’s commodity status into federal law, whether spot ETF flows compound or trickle, whether the network’s settlement usage grows enough to translate into real token demand against the escrow supply, and where Bitcoin drags the broader market. Those are the signals worth watching, and the IPO hint is not among them. This does not mean the remark is meaningless. It reveals something real about Ripple’s posture toward its community, a willingness to at least entertain the idea of connecting corporate success to holders, which is more than many companies would offer.
But revealing a posture is not the same as making a commitment, and the most useful thing a holder can do is to enjoy the signal for what it shows about Ripple’s attitude while declining to build any expectation on top of it. The community heard a promise. What Garlinghouse offered was a maybe, and in investing the difference is everything. An XRP holder is better served by evaluating the token on its actual merits, its use in payments, its regulatory position, its adoption, and its supply dynamics, than by speculating about an IPO reward that exists only as a hedged possibility.
That possibility is attached to an IPO that may never come, and that could, in some scenarios, hurt the token as much as help it. The hope is understandable. The discipline is to keep it in proportion. If Ripple ever announces a real program, holders can judge the terms then; until then, the “special arrangement” is a signal, not a strategy.
Frequently asked questions Did Ripple promise XRP holders a payout from its IPO? No. Ripple chief executive Brad Garlinghouse said that “if and when” Ripple goes public, the company might do “something special” for XRP holders, then immediately added that it was “not in the immediate term.” That was a hedged “maybe” offered in response to a direct question, not a plan, a program, or a commitment, and he declined to endorse any specific mechanism such as a token buyback. The community amplified the remark into something close to a promise, but no payout has been announced, no mechanism has been described, and the comment was explicitly conditional on an IPO that Garlinghouse describes as not a priority.
Does holding XRP give me any ownership of Ripple? No. Ripple and XRP are legally and financially separate assets. Ripple is a private technology company that builds payment and liquidity products, some of which use the XRP Ledger. XRP is the native cryptocurrency of the XRP Ledger, a decentralized blockchain that Ripple does not control. Holding XRP grants no shares in Ripple, no dividends, no voting rights, and no claim on the company’s profits or assets.
What could a “special arrangement” actually look like? The mechanisms the community imagines include preferential access to Ripple IPO shares for verified long-term XRP holders, long-term holding rewards for those who keep XRP for a defined period, and tokenized Ripple equity made available to eligible holders. All of these are unannounced and remain speculation instead of anything Ripple has offered. Each also faces serious obstacles, especially securities law, because linking token holding to equity benefits raises exactly the questions Ripple fought during its long legal battle over XRP. More modest possibilities, such as a governance gesture or simply structuring the business so more value flows through XRP, are more realistic than a direct equity windfall.
Is Ripple actually going to have an IPO? It is uncertain, and Garlinghouse has repeatedly described going public as not a priority. He has cited the weak post-listing performance of crypto-company peers and reports of a major exchange delaying its own plans, and he has argued that staying private preserves flexibility. This matters because the entire holder-benefit question is downstream of an IPO happening at all. Even the most generous imaginable reward is irrelevant unless Ripple first decides to go public and then chooses to extend something to holders.
Could a Ripple IPO actually be bad for XRP? It could, and this is the part the bullish framing tends to skip. An IPO would give institutions a direct way to own Ripple through regulated stock that offers dividends, financial transparency, and ownership of company assets, potentially drawing capital that might otherwise have flowed into XRP as a proxy for Ripple. Separately, as a public company answerable to quarterly earnings expectations, Ripple could face stronger incentives to monetize its large XRP escrow holdings more aggressively, adding long-term selling pressure on the token. Going public is therefore a double-edged sword for XRP, with credible downside as well as the hoped-for upside, and holders should weigh both.
What should XRP holders actually focus on? On the observable catalysts that truly move the token instead of the IPO hint. Those include whether the CLARITY Act passes and codifies XRP’s commodity status, whether spot XRP ETF flows compound or stall, whether the network’s settlement usage grows into real token demand against the escrow supply, and the direction of Bitcoin and the broader market. The “special arrangement” remark is best treated as a small signal about Ripple’s posture toward its community, given minimal weight in any actual view of XRP’s prospects. Evaluating XRP on its real merits, utility, regulatory position, adoption, and supply, is far sounder than positioning around a hedged maybe.
This article is information, not investment advice. Prices, corporate plans, and statements reflect reporting available as of June 28, 2026, and can change quickly. Brad Garlinghouse’s comments were conditional and did not constitute a commitment or a program. Nothing here is a recommendation to buy or sell XRP or any security. Verify current details from primary sources and consider your own circumstances before making any decision.
CLARITY Act by mohl odstranit právní nejistotu a otevřít cestu americkým penzijním fondům s majetkem kolem 56 bilionů USD k digitálním aktivům, včetně XRP. To by mohlo výrazně zúžit likviditu dostupnou k obchodování.
The CLARITY Act, currently under discussion in the United States, is gaining close attention in crypto markets due to its potential to deliver a much clearer regulatory framework for digital assets. Should the bill become law, many industry observers believe it could significantly reduce the legal uncertainty that has long deterred institutional investors from entering the space.
Why institutional capital is watching Market sources tracking industry data suggest that the CLARITY Act could be a game changer for the US crypto sector. According to this perspective, the bill may eliminate one of the major regulatory hurdles preventing American pension funds—which collectively manage around $56 trillion in assets—from accessing digital assets. These funds typically avoid assets without clear legal status due to strict compliance obligations.
At the heart of the debate lies the question of whether digital assets should be classified as securities or commodities. This lack of clarity keeps institutions from allocating capital to cryptos like XRP, presenting both legal and custodial challenges for major investors.
Glossary: The CLARITY Act is a legislative proposal in the US aiming to clarify the regulatory framework for digital assets. Its main purpose is to define which assets will be treated as securities and which as commodities, easing the compliance burden for market participants.
If the CLARITY Act takes effect, analysts believe it could establish a comprehensive framework for digital assets and bolster the standing of assets such as XRP among institutional investors.
Liquidity squeezes move into focus One notable aspect for XRP is that not all of its circulating supply is actively traded. Although the total supply is high, only a limited fraction is exchanged on markets. A substantial portion remains in the hands of long-term holders, is stored in institutional wallets, or is locked in escrow accounts, narrowing the readily accessible supply for trading.
This limited tradable supply means that even a modest influx of institutional capital into XRP, spurred by regulatory clarity, could rapidly tighten available liquidity. Market observers note that if demand outstrips accessible supply, upward price pressure could escalate swiftly.
Despite XRP’s large total supply, the actively traded amount remains restricted, so any surge in institutional demand could sharply reduce liquidity in the short term.
Time pressure mounts in Washington Meanwhile, reports indicate Congress is picking up the pace on the bill. Republican lawmakers are pushing to advance the CLARITY Act before the August recess, driven by a crowded legislative calendar that leaves little room for delay.
Once senators return to work on July 13, Congress will have only about 20 working days to deliberate, vote on the bill, and come to an agreement with the House of Representatives on the final version. This tight window is putting additional pressure on lawmakers to give the bill the necessary attention.
Within the digital asset industry, the CLARITY Act is viewed as one of the most significant regulatory moves in the US in recent years. Its passage could unlock far broader institutional participation—and with it, the prospect of reducing the legal fog that has hovered over the market, potentially making XRP a standout asset in the coming period.
Disclaimer: The information contained in this article does not constitute investment advice. Investors should be aware that cryptocurrencies carry high volatility and therefore risk, and should conduct their own research.
Williams jedná o koupi Momentum Midstream za zhruba 5,5 miliardy USD, uvedl Bloomberg. Dohoda by posílila přepravu plynu z Haynesville do exportních terminálů na pobřeží Mexického zálivu.
CompaniesJune 28 (Reuters) - U.S. pipeline operator Williams (WMB.N), opens new tab is in advanced talks to acquire rival natural gas pipeline operator Momentum Midstream for about $5.5 billion, Bloomberg News reported on Sunday, citing people familiar with the matter.
The Tulsa, Oklahoma-based company is putting the finishing touches on an agreement to buy Momentum from private equity firm EnCap Flatrock Midstream, the report said, adding that a deal could be announced in about a week.
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Reuters could not immediately verify the report. Williams Companies, Momentum Midstream and EnCap Flatrock Midstream did not immediately respond to a request for comment.
The deal would give Williams additional capacity to move gas from the Haynesville shale to U.S. Gulf Coast export terminals, the Bloomberg report said.
No final decision has been made and EnCap could still opt to retain the company, according to the report.
Williams is exploring acquiring U.S. natural gas production assets as it looks to secure supplies for its offerings to hyperscalers and data center clients, Reuters reported in February.
Momentum Midstream operates around 4,000 miles (6,437 km) of pipelines, serving more than 140 customers across its network, according to the company website, opens new tab. It also serves 10 liquefied natural gas facilities and 26 power plants.
Reporting by Bipasha Dey in Bengaluru; Editing by Edmund Klamann and Bill Berkrot
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Matrixdock rozšiřuje tokenizované zlato XAUm na síť Stellar a Stellar Development Foundation do něj přímo investuje v rámci diverzifikace pokladny. XAUm je krytý 1:1 fyzickým zlatem o ryzosti 99,99 % akreditovaným LBMA.
@matrixdock, Asia's leading real-world asset tokenization platform, has expanded its tokenized gold product XAUm to the @StellarOrg network. As part of the deal, the Stellar Development Foundation is making a direct investment in XAUm as part of its on-chain treasury diversification, reinforcing XAUm's role as a reserve-grade asset for institutional treasuries.
What Is XAUm and How Is It Backed?Each XAUm token is backed 1:1 by 99.99% purity LBMA-accredited physical gold, securely stored with custodians Brink's and Malca-Amit. Reserves are independently audited by Bureau Veritas, the same firm that verifies the world's largest gold ETFs, with Stellar smart contracts audited by OtterSec and Runtime Verification.
XAUm has grown to rank among the top four tokenized gold products globally and is Asia's largest, with over 88,000 unique on-chain addresses and 730,000 lifetime transactions across its ecosystem.
On Stellar, XAUm will be integrated with the Stellar DEX liquidity pools and lending markets, with on-chain liquidity support provided by Wave Digital Assets. XAUm-dedicated deposit vaults will also be launched, enabling institutional clients to deposit, hold, and earn XAUm natively.
Stellar's RWA Momentum BuildsThe XAUm expansion arrives as the total value of real-world assets and stablecoins on the Stellar network reaches $3.35 billion, a figure that includes tokenized treasury products and fiat-backed stablecoins. The milestone underscores Stellar's accelerating push to bridge traditional finance with blockchain infrastructure.
The Matrixdock deal follows a May 2026 collaboration between the Stellar Development Foundation and the Depository Trust and Clearing Corporation (DTCC), which announced plans to connect its tokenization service to the Stellar network as part of a broader multi-chain strategy.
Sources:
Matrixdock official press release via PR Newswire
Stellar network RWA market cap surpasses $3 billion, Crypto Briefing