Veteran short-seller James Chanos has officially closed his high-profile trade shorting MicroStrategy (MSTR) while holding long positions in Bitcoin. The decision, announced on November 7, 2025, came after MicroStrategy’s premium to its Bitcoin holdings plunged from 2.5x to just 1.17x, signaling that the stock’s price had realigned more closely with the value of its underlying assets.
MicroStrategy currently holds 641,205 BTC worth approximately $65.4 billion, against a few billion dollars of debt. Despite this, the company’s market capitalization remains around $76 billion. Its stock is down 16% in 2025, while Bitcoin itself has gained about 9% over the same period. According to analysts, the now-closed trade yielded estimated returns of 15% to 35%, demonstrating disciplined market timing amid volatile conditions.
Market strategist Peter Duan noted that Chanos’s move underscores a critical investment lesson — the erosion of Wall Street’s traditional information edge. Duan emphasized that successful short-sellers like Chanos thrive by managing asymmetric risks and identifying overextended valuations. He pointed out that MSTR and Japan-based Metaplanet both saw parabolic, retail-driven rallies disconnected from their fundamentals. Low institutional ownership in these stocks made them attractive short targets, as retail sentiment amplified volatility and correlation with Bitcoin’s price movements.
While Duan remains bullish on the long-term prospects of Bitcoin Treasury companies like MicroStrategy and Metaplanet, he cautioned that investors continue to underestimate their operational complexities. With short pressure easing, MSTR’s next major move will likely depend on Bitcoin’s performance. The episode serves as a reminder of how deeply corporate Bitcoin strategies are now shaping equity market behavior.
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2025-11-09 00:271mo ago
2025-11-08 19:061mo ago
Bitcoin ETFs Record Massive Outflows as Whales Exit Amid Market Uncertainty
Bitcoin exchange-traded funds (ETFs) faced their largest single-day outflow since August, signaling rising caution among institutional investors and major Bitcoin holders. According to SoSoValue data, U.S.-listed Bitcoin ETFs saw a staggering $558.4 million in net outflows, marking the biggest drawdown since August 1. This comes as Bitcoin struggles around the $102,000 level, reflecting waning market confidence despite steady prices.
Leading the exodus, Fidelity’s FBTC reported $256 million in outflows, while Ark Invest and 21Shares’ ARKB followed with $144 million, the fund’s largest outflow relative to its size. Even BlackRock’s IBIT ETF, typically more resilient, wasn’t spared—logging $131 million in withdrawals, its seventh outflow in eight trading sessions. Analysts suggest that macroeconomic uncertainty and profit-taking may be driving the pullback.
However, JPMorgan made a contrarian move by increasing its stake in BlackRock’s Bitcoin ETF by 64%, now holding 5.28 million shares worth $343 million as of September 30. The bank also maintains $68 million in call options and $133 million in put positions, showing a balanced yet opportunistic stance on Bitcoin’s volatility.
Adding to the market’s fragility, on-chain data indicates that long-term Bitcoin whales are offloading significant holdings. Capriole Investments co-founder Charles Edwards described the current environment as a “super whale exit phase,” with dormant wallets selling between $100 million and $500 million worth of BTC. Research firm K33 further revealed that “mega whales” have liquidated over $45 billion in the past month, hinting at widespread profit realization.
Despite the selloffs, optimism lingers. Michael Saylor’s bullish “Buy Now” call and James Chanos’ exit from bearish positions are fueling renewed confidence that Bitcoin could soon rebound from its current slump.
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2025-11-09 00:271mo ago
2025-11-08 19:081mo ago
Litecoin Price Eyes Breakout as Bulls Target $130 After 17% Surge
Litecoin (LTC) has captured renewed investor attention after an impressive 17% rebound in just one day, showcasing strong resilience in the crypto market. Currently trading near $101.02, LTC is testing a key resistance level at $102 — a decisive zone that could determine its next major move. A confirmed breakout above this barrier may trigger a bullish reversal, paving the way for a rally toward $130 in the coming weeks. The price structure aligns with a long-term falling wedge pattern, suggesting growing momentum for an upward breakout.
If Litecoin fails to close above $102, however, a temporary pullback toward $85 could occur before buyers regain momentum. Still, the broader technical outlook remains favorable, supported by strengthening indicators. The Directional Movement Index (DMI) shows the +DI at 24.76 surpassing the -DI at 21.92, signaling bullish control. Meanwhile, the Average Directional Index (ADX) at 26.41 confirms an intensifying trend, while the MACD’s bullish crossover further validates increasing market momentum.
Despite mild profit-taking reflected in the Spot Taker CVD data, Litecoin’s price stability near resistance highlights sustained buying pressure. The recent launch of Canary Litecoin ETFs on NASDAQ adds further optimism, signaling increasing institutional demand for LTC. This influx of interest could solidify Litecoin’s breakout potential and drive a sustained rally if bulls maintain control.
Overall, Litecoin’s technical setup points to continued bullish momentum, with growing confidence among traders and institutions alike. A decisive close above $102 could confirm a major trend reversal, setting LTC on course for a strong move toward $130. As market sentiment strengthens and profit-taking stabilizes, Litecoin appears well-positioned to extend its recovery and confirm its next bullish phase.
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2025-11-09 00:271mo ago
2025-11-08 19:101mo ago
Ethereum Price Faces Pressure as Weak On-Chain Metrics and ETF Outflows Limit Upside
Ethereum (ETH) has fallen about 12% over the past week, slipping after briefly climbing to $3,400. Analysts highlight key liquidity zones between $3,200 and $3,350, indicating the cryptocurrency could revisit that range before attempting a move toward $3,500. The decline reflects broader market uncertainty, with weak global economic indicators and risk-off sentiment pressuring digital assets. Disappointing earnings from major consumer firms and renewed concerns over inflated artificial intelligence valuations have added to bearish sentiment. The ongoing U.S. government shutdown—the longest in history—has also dragged down investor confidence, with consumer expectations sinking to their lowest since 1978, according to the University of Michigan survey.
On-chain data underscores Ethereum’s cooling ecosystem. Total value locked (TVL) has plunged to around $74.26 billion, marking a 24% drop over the past month—the lowest level since July. A major catalyst was the $120 million Balancer v2 DeFi exploit earlier this week. Trading volume fell 31.6% to $65.3 billion, while open interest slipped 3.4% to $38.85 billion. The OI-weighted funding rate, hovering near 0.0073%, reflects muted bullish leverage. DApp activity also declined 18% month-over-month to $80.7 million in October, signaling reduced network engagement and lower staking rewards.
Institutional demand remains sluggish, with U.S.-listed Ethereum spot ETFs seeing net outflows of $507.83 million in November. Corporate treasuries have also avoided new ETH allocations, underscoring weak institutional participation. While the upcoming Fusaka Upgrade in early December may offer a potential catalyst by improving scalability and security, Ethereum’s short-term outlook remains uncertain. Sustained recovery would require stronger macroeconomic conditions, renewed ETF inflows, and on-chain growth. Until then, ETH may continue consolidating near support zones, with limited potential for a breakout toward $3,900.
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Hedera’s native token, HBAR, continues to demonstrate impressive resilience despite facing multiple market crashes and failed recovery attempts. The altcoin remains steady above a key support level, bolstering investor confidence even as broader market sentiment leans bearish. However, uncertainty persists about how long HBAR can maintain this stability without stronger buying momentum.
The Chaikin Money Flow (CMF) indicator reveals that HBAR is still in the bearish zone below the zero line, signaling ongoing capital outflows. Although there has been a slight improvement, the inflows remain insufficient to shift market control away from sellers. This pattern suggests that until buying pressure consistently exceeds selling activity, HBAR’s price will stay under downward pressure. A gradual rise in inflows points to a slow return of investor interest, but it has yet to gain enough strength to influence the price trend decisively.
Similarly, the Relative Strength Index (RSI) supports this bearish outlook, staying below the neutral 50.0 mark. This indicates weak momentum and hesitation among traders to re-enter bullish positions. Without stronger market support, any short-term rally could face resistance and fail to sustain momentum. For HBAR to regain bullish traction, the RSI needs to move closer to neutral or above.
At present, HBAR trades at $0.174, just under the $0.175 resistance level. The token’s critical support sits at $0.162, a level that has successfully prevented deeper declines toward $0.154 in recent weeks. This zone continues to serve as a crucial foundation for potential recovery.
If overall market sentiment improves and capital inflows strengthen, HBAR could flip $0.175 into support, potentially sparking a rally toward $0.194 or even $0.200—marking a possible end to its current bearish phase.
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2025-11-09 00:271mo ago
2025-11-08 19:151mo ago
Trump Media Holds Over $1.3 Billion in Bitcoin as Crypto Strategy Expands
Trump Media and Technology Group (TMTG), the media company linked to U.S. President Donald Trump, has disclosed holding more than 11,500 Bitcoin valued at over $1.3 billion. This marks its largest confirmed crypto allocation and positions TMTG among the biggest corporate holders of Bitcoin globally. The move follows the company’s strategic decision to adopt Bitcoin as a core reserve asset, aimed at reducing reliance on traditional financial institutions that it claims have subjected it to discrimination and scrutiny.
TMTG’s pivot toward cryptocurrency mirrors a broader trend of companies using Bitcoin to safeguard against perceived risks in the banking system. Beyond Bitcoin, the company also reported owning around 756 million Cronos (CRO) tokens, valued at approximately $110 million. This investment highlights its growing partnership with Crypto.com, which has led to several blockchain-based initiatives, such as crypto exchange-traded products and promotional collaborations designed to enhance the firm’s digital presence.
Despite its significant crypto holdings, TMTG continues to face financial headwinds. The company posted a $54.8 million net loss in the third quarter of 2025, underscoring that its crypto strategy has served more as a political and operational statement than a short-term profit driver. Meanwhile, the Trump family and affiliated ventures have also ramped up their crypto exposure. Reports from Arkham Intelligence show Trump personally holds about $861,000 in digital assets, while related projects—including World Liberty Financial and Official Trump Meme—collectively control billions in cryptocurrencies. Together, these holdings signal a coordinated embrace of digital assets, reflecting the administration’s growing commitment to crypto as both a financial tool and a national policy priority.
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2025-11-09 00:271mo ago
2025-11-08 19:181mo ago
Solana Price Declines Amid Strong Bitcoin Correlation and Market Weakness
Solana (SOL) continues its downward trajectory, extending investor losses as bearish sentiment grips the broader cryptocurrency market. Despite brief recovery phases in recent months, the altcoin now faces renewed selling pressure, largely influenced by its close correlation with Bitcoin’s price action.
Currently, Solana’s correlation with Bitcoin stands at an exceptionally high 0.97, indicating that SOL’s movements closely mirror those of the leading cryptocurrency. With Bitcoin trading near the $100,000 mark and struggling to break higher, Solana’s price outlook remains vulnerable. The lack of bullish momentum in Bitcoin has stifled Solana’s potential for independent growth, fueling investor uncertainty about the altcoin’s near-term stability.
From an on-chain perspective, Solana’s Net Unrealized Profit and Loss (NUPL) metric has slipped into the capitulation zone—a sign that many investors are holding assets at a loss. Historically, this zone has marked pivotal turning points for SOL, as investors tend to hold rather than sell during downturns, which can help slow further declines. However, given its strong dependency on Bitcoin’s market direction, Solana’s NUPL could deteriorate further if Bitcoin fails to stabilize.
At the time of writing, Solana trades around $157, continuing a month-long downtrend. If bearish momentum persists, SOL could slide toward $150 or even $146, levels that might trigger renewed buying interest and a potential rebound toward $163 or $175. However, if Bitcoin’s weakness deepens, Solana could fall below $146, potentially testing the $140 zone and invalidating short-term recovery expectations.
With market sentiment hinging on Bitcoin’s performance, Solana investors are watching closely for signs of stabilization before anticipating any meaningful recovery.
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2025-11-09 00:271mo ago
2025-11-08 19:201mo ago
Hyperliquid Tests Borrowing and Lending Module on Hypercore Amid Security Concerns
Hyperliquid, a decentralized trading platform, is reportedly testing a borrowing and lending module on its Hypercore testnet—hinting at a significant expansion beyond its current perpetuals offering. On-chain researcher MLM revealed that the feature, labeled “BLP” (BorrowLendingProtocol), could introduce a native money-market layer to the Hyperliquid ecosystem.
According to MLM, the BLP testnet currently supports only USDC and PURR, but even limited asset integration indicates the foundation of a broader lending framework. If fully deployed, the module would enable users to borrow, supply, and withdraw assets directly within the Hyperliquid environment—creating a self-contained DeFi ecosystem.
MLM added that embedding a lending protocol could also allow Hyperliquid to roll out multi-margin trading safely. In this structure, traders’ margin positions would be backed by verifiable lending pools instead of isolated balance sheets. This model mirrors the transparent systems used by leading DeFi platforms, improving both risk management and leverage visibility.
A native lending layer would also expand Hyperliquid’s reach in the DeFi space, reducing the need for external lending protocols and consolidating user activity within its ecosystem. Such integration could strengthen liquidity flow, enhance capital efficiency, and attract traders seeking a seamless trading and borrowing experience.
However, while Hyperliquid explores innovation, users face growing security threats. A fake Hyperliquid mobile app recently appeared on the Google Play Store, despite the exchange not offering any official mobile application. Crypto investigator ZachXBT warned that the fraudulent app is a phishing scam designed to steal private keys and wallet credentials. He linked it to an Ethereum address responsible for stealing over $281,000 in assets.
This incident underscores the increasing sophistication of crypto-related scams. As Hyperliquid expands its ecosystem, users are urged to stay vigilant and download only verified software to safeguard their funds.
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2025-11-08 23:271mo ago
2025-11-08 17:311mo ago
ROSEN, A RANKED AND LEADING LAW FIRM, Encourages WPP plc Investors to Secure Counsel Before Important Deadline in Securities Class Action - WPP
WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of American Depositary Shares (“ADS” or “ADSs”) of WPP plc (NYSE: WPP) between February 27, 2025 and July 8, 2025, both dates inclusive (the “Class Period”), of the important December 8, 2025 lead plaintiff deadline.
SO WHAT: If you purchased WPP ADSs during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
WHAT TO DO NEXT: To join the WPP class action, go to https://rosenlegal.com/submit-form/?case_id=46121 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than December 8, 2025. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm achieved, at that time, the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.
DETAILS OF THE CASE: According to the complaint, defendants provided overwhelmingly positive statements to investors while, at the same time, disseminating materially false and misleading statements and/or concealing material adverse facts concerning the true state of WPP’s media arm; notably, that it was not truly equipped to handle the ongoing macroeconomic challenges while competing effectively and had instead begun to lose significant market share to its competitors. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the WPP class action, go to https://rosenlegal.com/submit-form/?case_id=46121 call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor’s ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
Contact Information:
Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827 [email protected]
www.rosenlegal.com
2025-11-08 23:271mo ago
2025-11-08 17:361mo ago
Camurus AB (publ) (CAMRF) Q3 2025 Earnings Call Transcript
Camurus AB (publ) (OTCPK:CAMRF) Q3 2025 Earnings Call November 6, 2025 8:00 AM EST
Company Participants
Fredrik Tiberg - President, CEO, CSO & Director
Anders Vadsholt - Chief Financial Officer
Richard Jameson - Chief Commercial Officer
Conference Call Participants
Viktor Sundberg - Nordea Markets, Research Division
Richard Ramanius - Redeye AB, Research Division
Romy O'Connor - Van Lanschot Kempen NV
Shan Hama - Jefferies LLC, Research Division
Georg Tigalonov-Bjerke - ABG Sundal Collier Holding ASA, Research Division
Suzanna Queckbörner - Handelsbanken Capital Markets AB, Research Division
Dan Akschuti - Pareto Securities AS, Research Division
Presentation
Operator
Welcome to Camurus' Q3 Report 2025. [Operator Instructions] Now I will hand the word over to CEO, Fred Tiberg, please go ahead.
Fredrik Tiberg
President, CEO, CSO & Director
Thank you so much, Einer, and hello, everyone. Welcome to our third quarter earnings call. It's a beautiful autumn day here in Lund, Sweden, where we are sending this from. I will assume that you have read our forward-looking statements going forward here. So the agenda for the call today is as follows: we start with third quarter highlights, move on to financial and commercial performance reviews, followed by an update on R&D and then we'll finish off with the key takeaways and Q&A. With me on the call today is Anders Vadsholt, Chief Financial Officer; and Richard Jameson, Chief Commercial Officer.
During the quarter, Camurus delivered strong profitability, continued progress on pipeline programs and prepared for the launch of our next commercial product. Starting then here with some highlights on the financial side. Our quarterly revenues increased by 18% year-on-year, 25% at constant exchange rates to SEK 575 million driven by higher Brixadi royalties. Profitability remains strong. We're growing 48% to SEK 245 million, increasing our cash position to SEK 3.5 billion. We maintained our profit guidance. However, due to the headwinds we have had, we have lowered our full year revenue guidance. The commercial performance
Continental Aktiengesellschaft (OTCPK:CTTAY) Q3 2025 Earnings Call November 6, 2025 6:30 AM EST
Company Participants
Max Westmeyer - Head of Investor Relations
Nikolai Setzer - Chairman of the Executive Board, Chief Sustainability Officer & CEO
Roland Welzbacher - CFO & Member of Executive Board
Conference Call Participants
Akshat Kacker - JPMorgan Chase & Co, Research Division
Christoph Laskawi - Deutsche Bank AG, Research Division
Horst Schneider - BofA Securities, Research Division
Monica Bosio - Intesa Sanpaolo Equity Research
Harry Martin - Sanford C. Bernstein & Co., LLC., Research Division
Thomas Besson - Kepler Cheuvreux, Research Division
Ross MacDonald - Citigroup Inc., Research Division
Michael Punzet - DZ Bank AG, Research Division
Michael Aspinall - Jefferies LLC, Research Division
Presentation
Max Westmeyer
Head of Investor Relations
Thank you very much. And welcome to all of you to our Q3 2025 results presentation. Today's call is hosted by our CEO, Nikolai Setzer; and our CFO, Roland Welzbacher. Both the press release and the presentation of today's call are available for download on our Investor Relations website. And I'd like to remind everyone that this conference call is for investors and analysts only. So if you do not belong to either of these groups, please disconnect now.
Following the presentation, we will conduct a Q&A session for sell-side analysts. [Operator Instructions] And before handing over, I want to briefly highlight some extraordinary effects that impacted our Q3 figures. As you're already used to it from the former AUMOVIO reporting, the signing of the sale of our original Equipment Solutions business within ContiTech has resulted in some accounting technicalities. Here, too, IFRS 5 applies and the assets and liabilities attributable to OESL were reclassified to assets and liabilities held for sale.
Furthermore, the sale has resulted in a write-down of the assets, which reduced the basis for depreciation. The depreciation of the new book values of
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2025-11-08 23:271mo ago
2025-11-08 17:421mo ago
Is Retail Sector ETF (XRT) Warning Us About Consumer?
“Intermediate and secular strength, with short-term caution — a bullish phase under pressure.”
I started to write about the Retail sector through the eyes of the Retail Sector ETF (NYSEARCA: XRT) for some time now.
On the Daily chart, the Retail Sector (XRT) broke down under the 50 DMA (blue) early October.
Here we are one month later, and despite QQQs and SPY having made new all-time highs mid-October, our Granny could not clear back over the 50-DMA.
We call that a warning or caution phase to be taken seriously.
Especially when it is XRT, which represents the consumer or 70% of the gross domestic product.
Now, XRT comes close to testing the 200-DMA (green.)
So, the bigger question is, what now?
This is where multiple timeframes help you step back and gain a more macro perspective.
On the weekly chart, the good news is that XRT remains above the 50-week moving average.
This could suggest that the correction is just about over.
However, I will continue to watch the Daily timeframe as bulls do not want to see the price break below that 200-DMA.
Momentum or the Real Motion indicator shows support at its 200-DMA (also green).
A break of price and momentum would be a case for even more caution.
A pop in price from these lows would be more encouraging.
Another interesting timeframe is the monthly chart.
These two long-term moving averages, 23-month (blue) and 80-month (green)—are essential components of MarketGauge’s technical analysis framework to identify major market regimes and long-term trend risk.
Trend Strength & Confirmation
If price is above both the 23- and 80-month MAs, the market is in a strong secular bull cycle.
If price fails the 23-month but holds the 80-month, it’s a warning phase—similar to mid-cycle corrections (2007, 2015, 2018).
A break below the 80-month MA signals a potential crisis-level or secular bear market (e.g., 2001, 2008).
Historical Examples
YearMarket Behavior23M vs. 80M LevelsOutcome2000–2002Dot-com collapseBroke 23M, then 80MSecular bear market2008Financial crisisViolated bothMajor systemic recession2011Debt downgrade scareTested 23M, held 80MMarket recovered2020COVID crashBriefly broke 23M, stayed above 80MV-shaped recoveryPresent (late 2024–2025)Still above both on SPYBull trend intact but stretchedWatching 23M as first warning level
Looking at XRT right now, the price is above the 23-month moving average.
Hence, retail remains in a bull trend.
Conclusion
Buyers still control the bigger picture, but sellers (or profit-taking) are pressuring the short-term.
This is often a “buy-the-dip in a long-term uptrend” environment, as long as the ETF holds above its weekly/monthly support.
If it reclaims the 50-DMA, momentum can resume higher.
If it loses both the 50-week and 23-month MAs—that’s when a real trend change risk emerges.
Twitter: @marketminute
The author may have a position in mentioned securities at the time of publication. Any opinions expressed herein are solely those of the author and do not represent the views or opinions of any other person or entity.
2025-11-08 23:271mo ago
2025-11-08 17:431mo ago
FCX Investor News: If You Have Suffered Losses in Freeport-McMoRan Inc. (NYSE: FCX), You Are Encouraged to Contact The Rosen Law Firm About Your Rights
WHY: Rosen Law Firm, a global investor rights law firm, announces an investigation of potential securities claims on behalf of shareholders of Freeport-McMoRan Inc. (NYSE: FCX) resulting from allegations that Freeport may have issued materially misleading business information to the investing public.
SO WHAT: If you purchased Freeport securities you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement. The Rosen Law Firm is preparing a class action seeking recovery of investor losses.
WHAT TO DO NEXT: To join the prospective class action, go to https://rosenlegal.com/submit-form/?case_id=45553 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
WHAT IS THIS ABOUT: On September 24, 2025, Freeport issued a press release entitled “Freeport Provides Update on PT Freeport Indonesia Operations.” It stated that Freeport “announced today an update on the status of the previously reported mud rush incident at the Grasberg Block Cave mine (GBC) in Indonesia. On September 20, 2025, PT Freeport Indonesia (PTFI) located two team members who were regrettably fatally injured in the September 8th incident.”
On this news, Freeport stock fell by 16.95% on September 24, 2025.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm achieved, at that time, the largest ever securities class action settlement against a Chinese Company. At the time Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
Contact Information:
Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827 [email protected]
www.rosenlegal.com
2025-11-08 23:271mo ago
2025-11-08 17:451mo ago
New Data from REZOLVE-AD Study of Rezpegaldesleukin Presented in Late-Breaking Oral Abstract Presentation at ACAAI 2025 Annual Scientific Meeting
Statistically significant and clinically meaningful improvements in mean ACQ-5 scores were reported at week 16 versus placebo in patients who had atopic dermatitis and a history of asthma
Extended dosing with rezpegaldesleukin q2w supports 24-week induction period for planned Phase 3 studies with improvement across major efficacy endpoints from Week 16 to 24, including EASI-75, EASI-90, and vIGA-AD
Data from long-term maintenance portion of REZOLVE-AD with 52 weeks of treatment expected in Q1 2026 from REZOLVE-AD study
Top-line Phase 2b data for rezpegaldesleukin in alopecia areata to be reported in December 2025
, /PRNewswire/ -- Nektar Therapeutics (Nasdaq: NKTR) today presented new data from the ongoing REZOLVE-AD Phase 2b study in a late-breaking oral abstract presentation at the American College of Allergy, Asthma & Immunology (ACAAI) 2025 Annual Scientific Meeting.
Rezpegaldesleukin is a first-in-class IL-2 pathway agonist and regulatory T-cell (Treg) biologic currently being studied in a Phase 2b study in moderate-to-severe atopic dermatitis (REZOLVE-AD) and a separate Phase 2b study in patients with severe-to-very-severe alopecia areata (REZOLVE-AA).
"Given that approximately one in four patients with atopic dermatitis also have asthma, improving asthma symptoms is a significant consideration in clinical treatment decisions," said lead author Dr. Jonathan Corren, Associate Clinical Professor of Medicine and Pediatrics at the David Geffen School of Medicine, University of California, Los Angeles. "The results with rezpegaldesleukin in patients with atopic dermatitis and comorbid asthma demonstrate that promotion of Treg activity may also have benefits to the lower airways, an observation which warrants further investigation."
The Phase 2b REZOLVE-AD trial enrolled 393 patients with moderate-to-severe atopic dermatitis, of which 99 patients also reported having a history of asthma with ACQ-5 data available at both baseline and week 16. A pre-planned analysis in the study evaluated scores from a validated Asthma Control Questionnaire (ACQ-5) at baseline and at the end of the 16-week induction period. For the patients reporting a history of asthma, all three rezpegaldesleukin doses demonstrated an overall reduction in mean observed ACQ-5 scores at week 16 with two dose arms (24 μg/kg q2w and 24 μg/kg q4w) achieving statistical significance (p<0.05) as compared to placebo. Patients in the placebo arm reported an overall worsening of mean ACQ-5 scores.
Improvements were more pronounced in patients with only partly controlled or uncontrolled asthma:
In patients with a baseline ACQ-5 score of 0.5 or higher (N=53), at least half of the patients experienced clinically significant improvement (≥0.5 point reduction) in ACQ-5 at Week 16 across all treatment arms as compared to 13% in the placebo arm.
Placebo-adjusted reductions of mean ACQ-5 scores in the subset of patients with baseline ACQ-5 score of 0.5 or higher ranged from 0.7 to 1.0.
Among the 25 patients with uncontrolled asthma at baseline (≥1.5 ACQ-5 score), all three active doses of rezpegaldesleukin demonstrated a meaningful improvement in mean observed ACQ-5 scores at Week 16 and all dose arms achieved statistical significance (p<0.05) as compared to placebo.
Placebo-adjusted reductions of mean ACQ-5 scores in this subset of patients with uncontrolled asthma at baseline (≥1.5 ACQ-5 score) ranged from 1.0 to 1.4.
For the 24 μg/kg q2w treatment arm, 75% of patients with uncontrolled asthma at baseline had a clinically significant improvement (≥0.5 points reduction) in ACQ-5 at Week 16.
"These observations of improvement in asthma control in REZOLVE-AD support the broad potential of rezpegaldesleukin's Treg mechanism across multiple T-cell mediated inflammatory diseases," said Jonathan Zalevsky, Ph.D., Chief Research and Development Officer of Nektar. "The data demonstrate that rezpegaldesleukin could offer a unique and differentiated innovative treatment for atopic dermatitis, particularly as these findings have not been observed with other biologic mechanisms recently approved or in advanced development."
Overall, in REZOLVE-AD, rezpegaldesleukin 24 μg/kg q2w resulted in statistically significant improvements in the primary and secondary endpoints on all measurements of atopic dermatitis disease control as compared to placebo. Rezpegaldesleukin resulted in improvement of mean percent change in EASI (p<0.001), EASI-75 (p<0.001), EASI-90 (p<0.05), vIGA-AD 0/1 (p<0.05), and NRS-Itch response (≥4-point reduction) (p<0.01) at Week 16. This treatment effect was observed across baseline characteristics for severity of disease, region, and asthma comorbidity.
Results presented today also included data for a total of 42 placebo patients who crossed over at Week 16 and continued in the study on a treatment escape arm to receive high dose rezpegaldesleukin (24 µg/kg q2w). Based on observed data from these patients, EASI-75 response rate at crossover week 24 was 60%; vIGA-AD 0/1 response rate at crossover week 24 was 33%; EASI-90 response rate at crossover week 24 was 37%; and Itch NRS response rate at crossover week 24 was 50% in patients with baseline score ≥ 4. These data support advancing the dose regimen of rezpegaldesleukin 24 μg/kg q2w with a 24-week treatment induction period into Phase 3 studies.
Details of the presentation at ACAAI are as follows:
Abstract ID: 7005
Oral Presentation: "Rezpegaldesleukin Novel Treg-Inducing Therapy Demonstrates Efficacy in Atopic Dermatitis and Asthma in Phase 2b Trial"
Session Title: Distinguished Industry & Late-breaking Oral Abstracts - Session 2
Presentation Date and Time: Saturday, November 8, 2025 at 5:33 PM ET
Location: Room W231
The full presentation made today at the 2025 ACAAI Scientific Meeting is available on Nektar's website at http://www.nektar.com under Scientific Publications.
About REZOLVE-AD Phase 2b Study
The ongoing global Phase 2b REZOLVE-AD study (NCT06136741) enrolled 393 patients with moderate-to-severe atopic dermatitis who had not previously received treatment with biologic or JAK inhibitor therapies. Patients were randomized across three different dose regimens of subcutaneous rezpegaldesleukin or placebo for a 16-week induction treatment period. Following this period, rezpegaldesleukin-treated patients who achieved EASI percent score reductions of >50 (EASI-50) were re-randomized (1:1) to continue at the same dose level on a q4w or q12w regimen through study week 52 in a blinded maintenance period.
The primary endpoint of the Phase 2b study is mean improvement in EASI score at the end of the 16-week induction treatment period. Secondary endpoints include the proportion of patients achieving Validated Investigator Global Assessment (vIGA-AD) of 0 or 1, those achieving EASI-75, and those achieving a greater than or equal to a 4-point improvement in Itch Numeric Rating Scale (NRS). Preplanned exploratory endpoints include a full range of translational biomarker measurements and a change in asthma control questionnaire - 5 (ACQ-5) scores for patients with comorbidity of asthma.
This trial was initiated in October 2023 and enrolled patients across approximately 110 sites globally with: 68% enrolled and treated in Europe, including Poland, Bulgaria, Germany, Czech Republic, Spain, Croatia and Hungary; 16% enrolled and treated in the United States; 11% enrolled and treated in Canada; and 5% enrolled and treated in Australia. Patient randomization was stratified based on baseline disease severity measured by vIGA-AD and geographic region. Key enrollment criteria in the study included a minimum EASI score of 16.0, a minimum Body Surface Area (BSA) of 10% and a minimum vIGA-AD of 3.
About Rezpegaldesleukin
Autoimmune and inflammatory diseases cause the immune system to mistakenly attack and damage healthy cells in a person's body. A failure of the body's self-tolerance mechanisms enables the formation of the pathogenic T lymphocytes that conduct this attack. Rezpegaldesleukin is a potential first-in-class resolution therapeutic that may address this underlying immune system imbalance in people with many autoimmune and inflammatory conditions. It targets the interleukin-2 receptor complex in the body to stimulate proliferation of immune-modulating cells known as regulatory T cells. By activating these cells, rezpegaldesleukin may act to bring the immune system back into balance.
In February 2025, the U.S. Food and Drug Administration (FDA) granted Fast Track designation for rezpegaldesleukin for the treatment of adult and pediatric patients 12 years of age and older with moderate-to-severe atopic dermatitis whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. In July 2025, the FDA granted Fast Track designation for rezpegaldesleukin for the treatment of severe alopecia areata (AA) in adults and pediatric patients 12 years of age and older who weigh at least 40 kg.
Rezpegaldesleukin is being developed as a self-administered injection for a number of autoimmune and inflammatory diseases. It is wholly owned by Nektar Therapeutics.
About Atopic Dermatitis
Atopic dermatitis is the most common type of eczema, affecting approximately 30 million people in the United States.1 AD is characterized by a defect in the skin barrier, which allows allergens and other irritants to enter the skin, leading to an immune reaction and inflammation.
About Nektar Therapeutics
Nektar Therapeutics is a clinical-stage biotechnology company focused on developing treatments that address the underlying immunological dysfunction in autoimmune and chronic inflammatory diseases. Nektar's lead product candidate, rezpegaldesleukin (REZPEG, or NKTR-358), is a novel, first-in-class regulatory T cell stimulator being evaluated in two Phase 2b clinical trials, one in atopic dermatitis, one in alopecia areata, and in one Phase 2 clinical trial in Type 1 diabetes mellitus. Nektar's pipeline also includes a preclinical bivalent tumor necrosis factor receptor type II (TNFR2) antibody and bispecific programs, NKTR-0165 and NKTR-0166, and a modified hematopoietic colony stimulating factor (CSF) protein, NKTR-422. Nektar, together with various partners, is also evaluating NKTR-255, an investigational IL-15 receptor agonist designed to boost the immune system's natural ability to fight cancer, in several ongoing clinical trials.
Nektar is headquartered in San Francisco, California. For further information, visit www.nektar.com and follow us on LinkedIn.
This press release contains forward-looking statements which can be identified by words such as: "could," "develop," "potential," "target," "address," "may" and similar references to future periods. Examples of forward-looking statements include, among others, statements regarding the therapeutic potential of, and future development plans for, rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422, and NKTR-255. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based only on our current beliefs, expectations and assumptions regarding the future of our business, future plans and strategies, anticipated events and trends, the economy and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our control. Our actual results may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. Important factors that could cause our actual results to differ materially from those indicated in the forward-looking statements include, among others: (i) our statements regarding the therapeutic potential of rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are based on preclinical and clinical findings and observations and are subject to change as research and development continue; (ii) rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are investigational agents and continued research and development for these drug candidates is subject to substantial risks, including negative safety and efficacy findings in future clinical studies (notwithstanding positive findings in earlier preclinical and clinical studies); (iii) rezpegaldesleukin, NKTR-0165, NKTR-0166, NKTR-422 and NKTR-255 are in clinical development and the risk of failure is high and can unexpectedly occur at any stage prior to regulatory approval; (iv) data reported from ongoing clinical trials are necessarily interim data only and the final results will change based on continuing observations; (v) the timing of the commencement or end of clinical trials and the availability of clinical data may be delayed or unsuccessful due to regulatory delays, slower than anticipated patient enrollment, manufacturing challenges, changing standards of care, evolving regulatory requirements, clinical trial design, clinical outcomes, competitive factors, or delay or failure in ultimately obtaining regulatory approval in one or more important markets; (vi) a Fast Track designation does not increase the likelihood that rezpegaldesleukin will receive marketing approval in the United States; (vii) patents may not issue from our patent applications for our drug candidates, patents that have issued may not be enforceable, or additional intellectual property licenses from third parties may be required; and (viii) certain other important risks and uncertainties set forth in our Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on November 7, 2025. Any forward-looking statement made by us in this press release is based only on information currently available to us and speaks only as of the date on which it is made. We undertake no obligation to update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.
November 08, 2025 6:14 PM EST | Source: The Rosen Law Firm PA
New York, New York--(Newsfile Corp. - November 8, 2025) - WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of American Depositary Shares ("ADS" or "ADSs") of WPP plc (NYSE: WPP) between February 27, 2025 and July 8, 2025, both dates inclusive (the "Class Period"), of the important December 8, 2025 lead plaintiff deadline.
SO WHAT: If you purchased WPP ADSs during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
WHAT TO DO NEXT: To join the WPP class action, go to https://rosenlegal.com/submit-form/?case_id=46121 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than December 8, 2025. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm achieved the largest ever securities class action settlement against a Chinese Company at the time. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs' Bar. Many of the firm's attorneys have been recognized by Lawdragon and Super Lawyers.
DETAILS OF THE CASE: According to the complaint, defendants provided overwhelmingly positive statements to investors while, at the same time, disseminating materially false and misleading statements and/or concealing material adverse facts concerning the true state of WPP's media arm; notably, that it was not truly equipped to handle the ongoing macroeconomic challenges while competing effectively and had instead begun to lose significant market share to its competitors. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the WPP class action, go to https://rosenlegal.com/submit-form/?case_id=46121 call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor's ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/273658
2025-11-08 23:271mo ago
2025-11-08 18:191mo ago
FLR DEADLINE ALERT: ROSEN, TRUSTED INVESTOR COUNSEL, Encourages Fluor Corporation Investors to Secure Counsel Before Important Deadline in Securities Class Action - FLR
November 08, 2025 6:19 PM EST | Source: The Rosen Law Firm PA
New York, New York--(Newsfile Corp. - November 8, 2025) - WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of securities of Fluor Corporation (NYSE: FLR) between February 18, 2025 and July 31, 2025, both dates inclusive (the "Class Period"), of the important November 14, 2025 lead plaintiff deadline.
SO WHAT: If you purchased Fluor securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
WHAT TO DO NEXT: To join the Fluor class action, go to https://rosenlegal.com/submit-form/?case_id=44868 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than November 14, 2025. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved, at that time, the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs' Bar. Many of the firm's attorneys have been recognized by Lawdragon and Super Lawyers.
DETAILS OF THE CASE: According to the lawsuit, throughout the Class Period, defendants made false and misleading statements and/or failed to disclose that: (1) costs associated with the Gordie Howe International Bridge ("Gordie Howe"), the Interstate 365 Lyndon B. Johnson ("I-635/LBJ") and Interstate 35E ("I-35") highways in Texas projects were growing because of, inter alia, subcontractor design errors, price increases, and scheduling delays; (2) the foregoing, as well as customer reduction in capital spending and client hesitation around economic uncertainty, was having, or was likely to have, a significant negative impact on Fluor's business and financial results; (3) accordingly, Fluor's financial guidance for the full year 2025 was unreliable and/or unrealistic, the effectiveness of Fluor's risk mitigation strategy was overstated, and the impact of economic uncertainty on Fluor's business and financial results was understated; and (4) as a result, defendants' public statements were materially false and misleading at all relevant times. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the Fluor class action, go to https://rosenlegal.com/submit-form/?case_id=44868 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor's ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/273652
Consider it "game over" for the company's recent wave of meme stock mania.
The past several years have been rough for Beyond Meat (BYND +16.81%), but that didn't stop the plant-based meat company's shares from becoming one of the top meme stocks last month. In fact, Beyond Meat's precarious state may be the reason behind last month's meme mania.
However, flash forward to now, and shares have already retreated considerably. Although the company itself may survive, there could be more pain ahead for investors.
Today's Change
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16.81
%) $
0.20
Current Price
$
1.39
A busted growth story for quite some time
Image source: Getty Images.
Up until the early 2020s, Beyond Meat was one of the most promising growth stocks. The rising popularity of plant-based diets pointed to further growth ahead. However, starting in 2021, the company's sales began to decline. This was due to a combination of competition from other alternative meat brands like Impossible Foods, coupled with the plant-based diet lifestyle trend peaking in popularity.
Already unprofitable, declining sales sank Beyond Meat deeper in the red. At first, existing cash covered these losses. Over the past two years, however, the company has had to sell more stock to raise money, leading to share dilution. Together, these factors caused shares to fall over 99% from their all-time high.
Why the meme stock run failed to last
Struggling and caught in a dilution spiral, Beyond Meat became a prime target for short-sellers. However, last month, as short interest spiked following the announcement of a highly dilutive debt restructuring plan, meme stock speculators started buying en masse to trigger a short squeeze.
This caused Beyond Meat to rally from around $0.55 per share to as much as $7.69 per share in a matter of days. However, after the company released lackluster preliminary quarterly results on Oct. 24, the "meme mania" quickly gave way to another massive sell-off.
What's next for Beyond Meat?
Thanks to the debt restructuring deal, Beyond Meat has staved off bankruptcy for now. However, unless the company quickly executes an effective turnaround plan, one that prioritizes profitability, the dilution spiral will likely continue. Existing shareholders would be wise to sell the stock; otherwise, stay away.
2025-11-08 22:271mo ago
2025-11-08 15:331mo ago
ROSEN, HIGHLY RANKED INVESTOR COUNSEL, Encourages aTyr Pharma, Inc. Investors to Secure Counsel Before Important Deadline in Securities Class Action - ATYR
WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of common stock of aTyr Pharma, Inc. (NASDAQ: ATYR) between January 16, 2025 and September 12, 2025, both dates inclusive (the “Class Period”), of the important December 8, 2025 lead plaintiff deadline.
SO WHAT: If you purchased aTyr Pharma common stock during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
WHAT TO DO NEXT: To join the aTyr Pharma class action, go to https://rosenlegal.com/submit-form/?case_id=46109 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than December 8, 2025. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions, but are merely middlemen that refer clients or partner with law firms that actually litigate the cases. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm achieved the largest ever securities class action settlement against a Chinese Company at the time. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.
DETAILS OF THE CASE: According to the complaint, defendants provided overwhelmingly positive statements to investors while, at the same time, disseminating false and misleading statements and/or concealing material adverse facts concerning the efficacy of Efzofitimod, particularly, the drug’s capability to allow a patient to completely taper their steroid usage. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the aTyr Pharma class action, go to https://rosenlegal.com/submit-form/?case_id=46109 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor’s ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
Contact Information:
Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827 [email protected]
www.rosenlegal.com
2025-11-08 22:271mo ago
2025-11-08 16:001mo ago
Want Passive Income From the Stock Market? 3 Magnificent Vanguard ETFs to Buy and Hold Forever
These funds could supercharge your passive income over time.
Dividend stocks are investments that pay a portion of profits back to shareholders, usually on a quarterly basis. A dividend exchange-traded fund (ETF) is a collection of dividend-paying stocks, all bundled together into a single investment.
By investing in a single dividend ETF, you can gain exposure to hundreds of stocks at once. The more shares you own, the more you'll receive in dividend payments -- potentially building a stream of passive income that pays thousands of dollars per year.
Not all dividend ETFs are created equal, but these three Vanguard funds can limit risk with ample diversification while paying out higher dividends.
Image source: Getty Images.
1. Vanguard Dividend Appreciation ETF
The Vanguard Dividend Appreciation ETF (VIG +0.14%) contains 337 stocks from companies with a history of increasing their dividend payments year after year. It pays quarterly dividends, and its most recent payment in early October was around $0.86 per share.
That may not sound like much, but once you've accumulated hundreds or even thousands of shares, it can add up. You also have the option to reinvest your dividend payments, making it easier to buy more shares. This can then have a snowball effect on earnings -- the more you invest, the more shares you'll own, the more you can reinvest in dividends, and so on.
Today's Change
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0.14
%) $
0.29
Current Price
$
215.64
In addition to dividend payments, you'll also earn standard investment returns like you would with any other stock or ETF. This fund has earned an average rate of return of 12.83% per year over the last 10 years, which is slightly higher than the market's historic average of 10% per year.
2. Vanguard High Dividend Yield ETF
The Vanguard High Dividend Yield ETF (VYM +0.50%) is similar in many ways to the Dividend Appreciation ETF. It's focused on stocks from companies that have high dividend yields, and it most recently paid a quarterly dividend of around $0.84 per share.
The key differences between the two funds come down to their size and performance. The High Dividend Yield ETF contains significantly more stocks, with 566 holdings. Greater diversification can help limit the impact of volatility, giving this fund an edge for more risk-averse investors.
NYSEMKT: VYMVanguard Whitehall Funds - Vanguard High Dividend Yield ETF
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0.50
%) $
0.70
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$
140.27
However, ETFs with more holdings can sometimes also earn lower returns, with lower-performing stocks dragging down the fund's total gains. Over the last 10 years, this fund has earned an average rate of return of 10.93% per year. While that's not a massive difference from the previous ETF's 12.83% average annual return, it can make a difference over time.
3. Vanguard International High Dividend Yield ETF
The Vanguard International High Dividend Yield ETF (VYMI +0.39%) contains stocks with the potential for above-average dividend yields, except it only includes international companies.
Investing in international stocks can have both advantages and risks. If you currently own only domestic companies, adding an international ETF can create more diversification. Sometimes, international markets are more favorable than the U.S. market, creating potential for higher returns.
That said, international stocks can sometimes be more volatile, too, especially during periods of economic or political instability. Just over 21% of the stocks in this particular ETF come from emerging markets, which are often less stable -- yet also have the potential for faster growth than developed markets.
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0.39
%) $
0.33
Current Price
$
86.10
The International High Dividend Yield ETF issues quarterly dividend payments, which have experienced greater fluctuations between quarters. While the previous two ETFs had fairly consistent payments in the $0.85 to $0.95 per share range, this fund has paid dividends of between $0.60 and $1.07 per share this year alone.
In short, international stocks can be more lucrative, but there's also a higher chance of short-term volatility. If you're looking for international exposure and are comfortable with somewhat higher risk, this ETF could earn higher-than-average dividends over time while diversifying your portfolio.
Investing in dividend ETFs is a smart way to gain exposure to dividend stocks, add some diversification to your portfolio, and build a source of passive income at the same time. By investing consistently and gradually increasing your stake, you could build a passive income stream worth thousands of dollars per year.
2025-11-08 22:271mo ago
2025-11-08 16:001mo ago
Inspire Medical Systems, Inc. (INSP) Faces Investor Suit Over Disastrous Inspire V Launch-- Hagens Berman
SAN FRANCISCO, Nov. 08, 2025 (GLOBE NEWSWIRE) -- Inspire Medical Systems, Inc. (NYSE: INSP) is now grappling with a proposed class-action lawsuit alleging the company misled investors about the commercial readiness and demand for its critical “next generation” sleep apnea device, the Inspire V. The litigation zeroes in on the disparity between the company's confident assurances and the subsequent disastrous rollout that led to a dramatic stock crash.
Prominent investor rights law firm Hagens Berman is investigating the alleged claims. The firm urges investors in Inspire who suffered significant losses to submit your losses now.
Class Period: Aug. 6, 2024 – Aug. 4, 2025
Lead Plaintiff Deadline: Jan. 5, 2026
Visit: www.hbsslaw.com/investor-fraud/insp
Contact the Firm Now: [email protected]
844-916-0895
Inspire Medical Systems, Inc. (INSP) Securities Class Action:
The case, styled City of Pontiac Reestablished General Employees’ Retirement System v. Inspire Medical Systems, Inc., et al., No. 0:25-cv-04247-PJS-ECW (D. Minn.), seeks to represent investors who purchased or otherwise acquired Inspire common stock between August 6, 2024 and August 4, 2025.
The complaint asserts that throughout the Class Period, Inspire repeatedly assured investors it had met all regulatory, technical, and commercial prerequisites for the Inspire V launch, while also touting high demand and a successful commercial proceeding.
However, the lawsuit claims the reality was starkly different and undisclosed to investors. The complaint alleges the Inspire V launch was, in fact, a disaster, crippled by minimal initial demand. This weak uptake, according to the suit, was due to the company’s customers already being flush with inventory of older, unsold Inspire IV devices. Furthermore, the complaint suggests Inspire had allegedly neglected basic steps necessary to ensure the new device’s swift adoption by clinicians and payors.
Investors allegedly learned the truth on August 4, 2025. That day, Inspire revealed that the Inspire V launch faced an “elongated timeframe” due to previously undisclosed headwinds.
Inspire explained that “many centers did not complete the training, contracting and onboarding criteria required prior to the purchase and implant of Inspire V.”
The company also said that, although Inspire V’s CPT code was approved for Medicare patients, “software updates for claims submissions and processing did not take effect until July 1.” This meant that implanting centers could not bill for those procedures until July 1 and, as a result, many centers opted to continue treating patients with the older generation Inspire IV.
Inspire further explained that demand for Inspire V was plagued by customers’ need to “burn down” Inspire IV inventory, a headwind that would continue to negatively impact demand for Inspire V.
Lastly, as a result the disastrous launch, Inspire slashed its 2025 earnings guidance by a whopping 80% to just $0.40 to $0.50 per share.
The news sent Inspire shares crashing $42.04 the next day, a decline of roughly 32%.
“We’re focused on investors’ losses and whether Inspire may have intentionally misled investors about headwinds adversely affecting the next generation launch and the dramatic negative effect on the company’s earnings potential,” said Reed Kathrein, the Hagens Berman partner leading the firm’s investigation.
If you invested in Inspire and have substantial losses, or have knowledge that may assist the firm’s investigation, submit your losses now »
If you’d like more information and answers to frequently asked questions about the Inspire case and our investigation, read more »
Whistleblowers: Persons with non-public information regarding Inspire should consider their options to help in the investigation or take advantage of the SEC Whistleblower program. Under the new program, whistleblowers who provide original information may receive rewards totaling up to 30 percent of any successful recovery made by the SEC. For more information, call Reed Kathrein at 844-916-0895 or email [email protected].
About Hagens Berman
Hagens Berman is a global plaintiffs’ rights complex litigation firm focusing on corporate accountability. The firm is home to a robust practice and represents investors as well as whistleblowers, workers, consumers and others in cases achieving real results for those harmed by corporate negligence and other wrongdoings. Hagens Berman’s team has secured more than $2.9 billion in this area of law. More about the firm and its successes can be found at hbsslaw.com. Follow the firm for updates and news at @ClassActionLaw.
Contact:
Reed Kathrein, 844-916-0895
2025-11-08 22:271mo ago
2025-11-08 16:061mo ago
GN Store Nord A/S (GNNDY) Q3 2025 Earnings Call Transcript
GN Store Nord A/S (OTCPK:GNNDY) Q3 2025 Earnings Call November 6, 2025 5:00 AM EST
Company Participants
Rune Sandager - Head of Investor Relations
Peter Karlstromer - Chief Executive Officer
Soren Jelert - Chief Financial Officer
Conference Call Participants
Andjela Bozinovic - BNP Paribas, Research Division
Carsten Madsen - Danske Bank A/S, Research Division
Veronika Dubajova - Citigroup Inc., Research Division
Martin Parkhoi - SEB, Research Division
Niels Granholm-Leth - DNB Carnegie, Research Division
Martinien Rula - Jefferies LLC, Research Division
Susannah Ludwig - Sanford C. Bernstein & Co., LLC., Research Division
Julien Ouaddour - BofA Securities, Research Division
Martin Brenoe - Nordea Markets, Research Division
Richard Felton - Goldman Sachs Group, Inc., Research Division
Oliver Metzger - ODDO BHF Corporate & Markets, Research Division
Presentation
Rune Sandager
Head of Investor Relations
Hello, everyone, and welcome to GN's conference call in relation to our Q3 report announced this morning. Participating in today's call is Group CEO, Peter Karlstromer; Group CFO, Soren Jelert; and myself, Rune Sandager, Head of Investor Relations.
The presentation is expected to last about 20 minutes, after which we'll turn to the Q&A session. The presentation is already uploaded on gn.com. And with that, I'm happy to hand over to Peter for some opening remarks.
Peter Karlstromer
Chief Executive Officer
Thank you, Rune, and thanks to all of you for joining us today. Let me start with the group highlights on Slide 4. In Q3, we delivered a solid quarter with 1% organic revenue growth, driven by market share gains and strong performance across our divisions.
Our execution led to a healthy margin and cash flow development, allowing us to reconfirm our guidance for the year. In Hearing, the rollout of ReSound Vivia is continuing progressing very well. Vivia's strong differentiation and our solid commercial execution led to broad-based market share gains and 7% organic growth.
Overall, we are
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Heidelberg Materials AG (HDLMY) Q3 2025 Sales Call Transcript
Heidelberg Materials AG (OTCPK:HDLMY) Q3 2025 Sales Call November 6, 2025 7:00 AM EST
Company Participants
Christoph Beumelburg - Director of Group Communication & Investor Relations
Dominik von Achten - Chairman of Managing Board
René Aldach - CFO & Member of the Managing Board
Conference Call Participants
Luis Prieto - Kepler Cheuvreux, Research Division
Benjamin Rada Martin - Goldman Sachs Group, Inc., Research Division
Elodie Rall - JPMorgan Chase & Co, Research Division
Tom Zhang - Barclays Bank PLC, Research Division
Pujarini Ghosh - Sanford C. Bernstein & Co., LLC., Research Division
Julian Radlinger - UBS Investment Bank, Research Division
Cedar Ekblom - Morgan Stanley, Research Division
Anna Schumacher - BNP Paribas, Research Division
Arnaud Lehmann - BofA Securities, Research Division
Arnaud Pinatel - On Field Investment Research LLP
Sven Edelfelt - ODDO BHF Corporate & Markets, Research Division
Presentation
Operator
Ladies and gentlemen, welcome to the Heidelberg Materials Third Quarter 2025 Trading Update Conference Call. I'm Lorenzo, the Chorus Call operator. [Operator Instructions] The conference is being recorded. [Operator Instructions] The conference must not be recorded for publication or broadcast.
At this time, it's my pleasure to hand over to Christoph Beumelburg. Please go ahead.
Christoph Beumelburg
Director of Group Communication & Investor Relations
Thank you, operator. Good morning, good afternoon, everyone, listening into our Q3 earnings call. Pleased to report the numbers that we published this morning. As always, we have in the room, Dominik, our CEO; Rene, our CFO; and from the IR team, Robert and Ozan and myself. So happy to receive your questions after the prepared remarks. And for those, I hand over to Dominik.
Dominik von Achten
Chairman of Managing Board
Yes, Chris, thanks a lot. Welcome, everybody. From our side, great to hear you and have you on the call. Let me just go through the presentation quickly, and then we get to your numbers. Good quarter for us. I think revenue up
SES S.A. (OTCPK:SGBAF) Q3 2025 Earnings Call November 6, 2025 8:00 AM EST Company Participants Christian Kern - Head of Investor Relations Adel Al-Saleh - Chief Executive Officer Elisabeth Pataki - Chief Financial Officer Conference Call Participants Paul Sidney - Joh. Berenberg, Gossler & Co. KG, Research Division Terence Tsui - Morgan Stanley, Research Division Ben Rickett - New Street Research LLP Roshan Ranjit - Deutsche Bank AG, Research Division Nick Dempsey - Barclays Bank PLC, Research Division Aleksander Peterc - Sanford C.
2025-11-08 22:271mo ago
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Pfizer wins $10 billion bidding war for obesity drug developer
U.S. drugmaker Pfizer has clinched a $10 billion deal for obesity drug developer Metsera, capping a fierce biotech bidding war between the New York-based pharma giant and Danish rival Novo Nordisk.
Metsera accepted a sweetened offer from Pfizer late on Friday, citing U.S. antitrust risks in Novo’s bid that it had previously called superior. The Danish obesity drug behemoth said on Saturday it would exit the race.
The bidding war win hands Pfizer a way into the lucrative obesity drug market, even if Metsera’s treatments remain years from hitting the market. It marks a blow for Novo as it tries to claw back lost ground against U.S. rival Eli Lilly.
A Pfizer research facility is shown in the La Jolla neighborhood of San Diego, California, U.S., September 30, 2025. REUTERS
Twists and turns in a biotech bidding war
Pfizer appeared to have locked up the deal in September before Novo jumped in last week with an unsolicited offer, sparking a fight for a coveted asset in the growing weight-loss market. Pfizer is trying to gain a toehold in obesity to overcome past in-house stumbles in developing weight-loss drugs.
Pfizer has agreed to pay $86.25 per share in cash, a premium of 3.69% to Metsera’s Friday close, Metsera said in a statement. The offer includes $65.60 per share in cash and a contingent value right entitling holders to additional payments of up to $20.65 per share in cash.
Novo Nordisk on Saturday said it would not be making an increased offer.
“Following a competitive process and after careful consideration, Novo Nordisk will not increase its offer to acquire Metsera,” the Danish drugmaker said in a statement.
Novo added that it is advancing its own pipeline of treatment options for obesity, and that it would “continue to assess opportunities for business development and acquisitions … that further its strategic objectives.”
The logo of Danish pharmaceutical company Novo Nordisk is seen on a sign outside their headquarters in Bagsvaerd, Denmark, on February 5, 2025. Ritzau Scanpix/AFP via Getty Images
A source close to Novo said that its last unsuccessful bid had been the “maximum value” of Metsera and that the firm remained confident in its own obesity drug pipeline. The deal was never “do or die” for Novo.
“This was always a bolt-on acquisition for Novo,” the person said.
‘Unacceptably high legal and regulatory risks’
The escalating M&A game sent Metsera’s shares surging over the last week. From just before Novo stepped in with its bid through Friday’s close, Metsera shares gained nearly 60%, sending its market value to $8.75 billion.
For a time, it appeared Novo had the inside track. Novo has been trying to recover its once-commanding position in obesity drugs that it lost to Eli Lilly.
Metsera, in its Friday statement, said Novo’s proposal presented “unacceptably high legal and regulatory risks” compared to the proposed merger with Pfizer, citing a call from the U.S. Federal Trade Commission to discuss the risks of a transaction with Novo. The regulator sent a letter earlier this week to Novo and Metsera, saying their proposed deal ran the risk of violating U.S. antitrust laws.
Logos of Pfizer at the company’s booth at the 8th China International Import Expo (CIIE) in Shanghai, China, November 6, 2025 REUTERS
Novo said in its statement that it believed that the structure of its offer was “compliant with antitrust laws”.
In a statement, Pfizer said it was pleased to have reached a revised agreement with Metsera, and expects to close the merger soon after Metsera’s November 13 shareholder meeting.
‘Game of Thrones’ style bidding war for Metsera
Bernstein analyst Courtney Breen said the $10 billion price rested on optimistic assumptions about the future performance of Metsera, saying Pfizer would need to assume $11 billion in revenue by 2040, nearly double Metsera’s current projections. She pointed to growing scepticism around long-term GLP-1 pricing, which could compress margins.
Metsera’s board recommended its shareholders approve the amended Pfizer offer. The biotech company currently loses money and analysts expect additional losses while its drugs are still in development.
Flags with the logos of Danish drugmaker Novo Nordisk, maker of the blockbuster diabetes and weight-loss treatments Ozempic and Wegovy are pictures while the company presents the annual report at Novo Nordisk in Bagsvaerd, Denmark, on February 5, 2025. Ritzau Scanpix/AFP via Getty Images
The bidding war between Pfizer and Novo lifted the price from Pfizer’s $7.3 billion offer in September. Former Pfizer research-and-development chief John LaMattina told Reuters the battle was reminiscent of Pfizer’s 2000 hostile takeover of Warner-Lambert for $90 billion in an effort to gain control of Lipitor, a cholesterol-lowering drug.
“While this is a smaller deal, Pfizer must believe that Metsera’s pipeline is key for its future,” he said.
Analysts and investors pointed to the unusually fierce fight to gain control of Metsera, whose early-stage obesity treatments remain unproven but could be key in a market some analysts estimate will hit $150 billion by early next decade.
“This is a Game of Thrones-level of play,” Peter Kolchinsky, managing partner at RA Capital, a top-20 Metsera shareholder, before the final bid was accepted.
Metsera’s experimental obesity drugs, MET-097i, a GLP-1 injectable, and MET-233i, which mimics the pancreatic hormone amylin, are projected to reach $5 billion in combined peak sales, according to Leerink Partners analyst David Risinger.
2025-11-08 22:271mo ago
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RS Group plc (EENEF) Q2 2026 Earnings Call Transcript
Thanks very much, and good morning, everyone. Welcome to the RS Group Interim Results Call for the 6-month period ending 30th September 2025, and thank you all for joining us this morning.
The presentation should take around 30 minutes, and then we'll have some time at the end for questions. But we'll try and make sure that we finish the call by no later than 10:00.
I'm going to start by summarizing our pleasing first half performance. Kate will then run through our in-line financials and what's driving them, both at a group and a regional level. Then I'll conclude by sharing with you the good underlying progress that we're making as we make the business better at RS and position ourselves to accelerate growth, improve efficiency, and drive better operating leverage over time.
But before we get into the details of this morning's presentation, we'd like to start our meetings, virtual or physical, at RS with a health and safety moment and a values highlight. So although we're virtual, please make sure you do take a safety moment to identify your nearest exit and safest evacuation route in the event of an emergency.
For our values highlight, I would just like to call out and celebrate our new multi-year global partnership with SolarAid to support their mission to light up lives across rural Africa. As our new global charity partner, their and our purposes and values are completely aligned that is one team delivering brilliantly, doing the right
2025-11-08 22:271mo ago
2025-11-08 16:161mo ago
Evolus, Inc. (EOLS) Q3 2025 Earnings Call Transcript
Q3: 2025-11-05 Earnings SummaryEPS of -$0.15 beats by $0.04
|
Revenue of
$68.97M
(12.90% Y/Y)
beats by $1.55M
Evolus, Inc. (EOLS) Q3 2025 Earnings Call November 5, 2025 4:30 PM EST
Company Participants
Nareg Sagherian - Head of Global Investor Relations & Corporate Communications
David Moatazedi - President, CEO & Director
Rui Avelar - Chief Medical Officer and Head of Research & Development
Tatjana Mitchell - Chief Financial Officer
Conference Call Participants
Annabel Samimy - Stifel, Nicolaus & Company, Incorporated, Research Division
Alyssa Larios - Leerink Partners LLC, Research Division
Navann Ty Dietschi - BNP Paribas, Research Division
Uy Ear - Mizuho Securities USA LLC, Research Division
Douglas Tsao - H.C. Wainwright & Co, LLC, Research Division
Serge Belanger - Needham & Company, LLC, Research Division
Sam Eiber - BTIG, LLC, Research Division
Presentation
Operator
Good afternoon, everyone, and thank you for standing by. Welcome to Evolus' Third Quarter Earnings Conference Call. [Operator Instructions] As a reminder, today's conference is being recorded and webcast live. [Operator Instructions]
I would now like to turn the conference over to Nareg Sagherian, Vice President and Head of Global Investor Relations and Corporate Communications. Please go ahead.
Nareg Sagherian
Head of Global Investor Relations & Corporate Communications
Thank you, operator, and welcome to everyone joining us on today's call to review Evolus' third quarter financial results. Our third quarter press release is now on our website at evolus.com. With me today are David Moatazedi, President and Chief Executive Officer; Tatjana Mitchell, Chief Financial Officer; and Rui Avelar, Chief Medical Officer and Head of R&D.
Today's call will include forward-looking statements. Actual results may differ materially due to risks and uncertainties outlined in our earnings press release and SEC filings. These forward-looking statements are based on current assumptions, and we undertake no obligation to update them. Additionally, we will discuss certain non-GAAP financial measures. These measures should be considered in addition to and not as a substitute for our GAAP results. A reconciliation of GAAP to non-GAAP
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Caterpillar Inc. (CAT) Analyst/Investor Day Transcript
Caterpillar Inc. (CAT) Analyst/Investor Day November 4, 2025 10:00 AM EST
Company Participants
Alex Kapper - Vice President of Investor Relations
Joseph Creed - CEO & Director
Jason Kaiser - Group President
Anthony Fassino - Group President of Construction Industries Group
Denise Johnson - Group President of Resource Industries
Bob De Lange - Group President of Services, Distribution & Digital
Andrew R. Bonfield - Chief Financial Officer
Conference Call Participants
Jamie Cook - Truist Securities, Inc., Research Division
Angel Castillo Malpica - Morgan Stanley, Research Division
Kyle Menges - Citigroup Inc., Research Division
Jerry Revich
Jairam Nathan - Daiwa Securities Co. Ltd., Research Division
Mircea Dobre - Robert W. Baird & Co. Incorporated, Research Division
Stephen Volkmann - Jefferies LLC, Research Division
Charles Albert Dillard - Sanford C. Bernstein & Co., LLC., Research Division
Robert Wertheimer - Melius Research LLC
Michael Feniger - BofA Securities, Research Division
Adam Seiden - Barclays Bank PLC, Research Division
Kristen Owen - Oppenheimer & Co. Inc., Research Division
Steven Fisher - UBS Investment Bank, Research Division
Tami Zakaria - JPMorgan Chase & Co, Research Division
Sabahat Khan - RBC Capital Markets, Research Division
Michael Shlisky - D.A. Davidson & Co., Research Division
Presentation
Alex Kapper
Vice President of Investor Relations
Good morning, everyone, and welcome to Caterpillar's 2025 Investor Day, the next 100 years. I'm Alex Kapper, Vice President, Investor Relations, and we're pleased to host you, whether you're joining online or in the room. And we're really excited to share with you how we see the next chapter of our story unfold. Just a few quick reminders before we get started. We've already conducted the safety briefing here in the room, and so I'd encourage anyone joining remotely to be aware of their surroundings and their local safety protocols.
During our event today, we'll make forward-looking statements, which are subject to risks and uncertainties. We'll make assumptions that could cause our actual results to be different
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The 1 Number That Shows Why Alphabet Is a Buy Today
In the competitive tech stock landscape, Alphabet ( NASDAQ:GOOG ) stands out because of its diverse revenue streams, from search advertising to cloud computing.
2025-11-08 22:271mo ago
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Monumental Milestones at the 2025 CNO Financial Indianapolis Monumental Marathon
, /PRNewswire/ -- A record-breaking field of more than 17,500 runners filled the streets of downtown Indianapolis today for the 18th annual CNO Financial Indianapolis Monumental Marathon, Half Marathon and 5K. The 13th consecutive sellout of the event showcased elite performances, including a new men's marathon course and event record and 14 athletes achieving qualifying times for the 2028 U.S. Olympic Team Trials – Marathon.
The Men's Champion, Joseph Whelan, broke the tape in 2:12:29, setting a new men's marathon course record and solidifying his place among the fastest marathoners ever to race in Indianapolis. On the women's side, Amanda Mosborg delivered a victory in 2:32:01, leading a strong field of competitors that included several returning champions and Trials qualifiers.
In total, 14 athletes earned 2028 U.S. Olympic Team Trials qualifying marks in the marathon distance, further establishing the CNO Financial Indianapolis Monumental Marathon as a key stop on the national competitive circuit.
Beyond the elite performances, the 2025 event featured a new start line on West Street, the largest marathon field in event history and the 10th anniversary of CNO Financial Group's title sponsorship. More than 6,600 marathoners earned their finisher medals and participants represented all 50 states and 22 countries, underscoring the event's growing global reach.
Results:
CNO Financial Indianapolis Monumental Marathon
Men's Champion: Joseph Whelan of Webster, N.Y., broke the finish tape and set a new course record with a winning time of 2:12:29. Ben Decker of Cambridge, Mass., and Andrew Bowman of Ferndale, Mich., finished second and third in a time of 2:15:23 and 2:15:33, respectively.
Women's Champion: Amanda Mosborg of St. Paul, Minn., finished first overall in a time of 2:32:01. Lucy Dobbs of Indianapolis crossed the line second with a time of 2:32:42, and Anna Benedettini of Virginia Beach, Va., finished third, coming in at 2:33:12.
CNO Financial Indianapolis Monumental Half Marathon
Men's Champion: Skylar Stidam of Bloomington, Ind., led the men's race and finished first in a time of 1:02:47. Second-place finisher Curtis Eckstein of Batesville, Ind., ran a time of 1:03:06, and third-place finisher Alec Basten of St. Louis, Mo., crossed the line in a time of 1:03:15.
Women's Champion: Carrie Ellwood of Boulder, Colo., won the women's race in a time of 1:08:33. Kasandra Parker of Waverly, Iowa, finished in second place with a time of 1:10:18, and Molly Grabill of Lafayette, Colo., finished in third at 1:11:00.
CNO Financial Indianapolis Monumental 5K
Men's Champion: Scott Spaanstra of Indianapolis, in 14:38.
Women's Champion: Sammy McClintock, Flagstaff, Ariz., in 16:17.
Other Highlights:
The 2025 event featured the 13th consecutive sellout and welcomed 17,500 participants from every U.S. state and 22 countries.
For the second consecutive year, the CNO Financial Indianapolis Monumental Marathon featured a record number of marathon finishers in the largest field ever.
Beyond Monumental's Run for a Cause program saw more than 240 participants run with a charity, such as Team World Vision, American Foundation for Suicide Prevention, International Justice Mission and more, all of which served to raise funds and awareness as they trained for the race.
This marks CNO Financial Group's 10th year as the title sponsor of its hometown marathon. CNO's partnership with Beyond Monumental underscores the organizations' shared commitment to health, wellness and the central Indiana community. The sponsorship continues to provide significant growth opportunities for Indy's premier running event.
Full results, when available, can be found here.
Plans are already underway for next year's event, scheduled for Saturday, Nov. 7, 2026. Participants can secure their spot for 2026 this weekend at monumentalmarathon.com. Registration closes Sunday, Nov. 9 and will reopen for the tradition of special Monumental Resolution pricing on Jan. 1, 2026.
About Beyond Monumental
Beyond Monumental, the 501(c)3 non-profit responsible for the CNO Financial Indianapolis Monumental Marathon, provides the Indianapolis community with a complement of activities built around their premiere event that promotes healthy living & fitness for all ages. Beyond Monumental gives back to the Indianapolis community by supporting youth programming that reinforces healthy lifestyles for young people, with an emphasis on working with urban students and Indianapolis Public Schools, donating over $1.7 million since inception. The CNO Financial Indianapolis Monumental Marathon is a top 15 marathon in the US and is nationally recognized by Runners' World as one of "Ten Great Marathons for First Timers". The 19th annual running is scheduled for Nov. 7, 2026. For more information, please visit beyondmonumental.org.
About CNO Financial Group
CNO Financial Group, Inc. (NYSE: CNO) secures the future of middle-income America. CNO provides life and health insurance, annuities, financial services and workforce benefits solutions through our family of brands, including Bankers Life, Colonial Penn, Optavise and Washington National. Our customers work hard to save for the future, and we help protect their health, income and retirement needs with 3.3 million policies and $38.3 billion in total assets. Our 3,300 associates, 4,900 exclusive agents and more than 6,500 independent partner agents guide individuals, families and businesses through a lifetime of financial decisions. For more information, visit CNOinc.com.
SOURCE CNO Financial Group
2025-11-08 22:271mo ago
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Musk is "maniacally dedicated to Tesla": ARK Strategist
About Yahoo Finance: Yahoo Finance provides free stock ticker data, up-to-date news, portfolio management resources, comprehensive market data, advanced tools, and more information to help you manage your financial life. - Get the latest news and data at finance.yahoo.com - Download the Yahoo Finance app on Apple (https://apple.co/3Rten0R) or Android (https://bit.ly/3t8UnXO) - Follow Yahoo Finance on social: X: http://twitter.com/YahooFinance Instagram: https://www.instagram.com/yahoofinance/?hl=en TikTok: https://www.tiktok.com/@yahoofinance?lang=en Facebook: https://www.facebook.com/yahoofinance/ LinkedIn: https://www.linkedin.com/company/yahoo-finance
John D. Rockefeller once said, "Do you know the only thing that gives me pleasure? It's to see my dividends coming in." While I personally find many other things more pleasurable than seeing dividend payments deposited in my brokerage account, I agree that there's something very satisfying about getting paid for work someone else did.
Given my fondness for dividend stocks, I own many of them. However, my favorite by far is Realty Income (O +0.88%). Here's why.
Image source: Getty Images.
The epitome of what a dividend stock should be
Realty Income is a dividend lover's dream stock. One thing that sets the real estate investment trust (REIT) apart from others is its dividend payment frequency. While most companies pay dividends quarterly, Realty Income is a monthly dividend stock. That payment frequency enables it to delight dividend investors every single month.
The REIT also stands out for how often it increases its dividend. While many companies strive to increase their payouts annually, Realty Income has raised its payment for 112 consecutive quarters. It has hiked its dividend by as much as six times in some years. Overall, Realty Income has raised its dividend 132 times since its public market listing in 1994 (including five times this year), growing it at a 4.2% compound annual rate.
Today's Change
(
0.88
%) $
0.49
Current Price
$
56.83
Another great aspect of Realty Income's dividend is its yield. It's currently at 5.7%, which is several times higher than the S&P 500's yield (1.2%). That higher yield enables me to generate a lot more income from every dollar I invest in the REIT compared to lower-yielding options.
Realty Income backs its high-yielding payout with a high-quality real estate portfolio and rock-solid balance sheet. Meanwhile, its strong financial profile puts it in an excellent position to continue growing its portfolio and dividend.
That's why, of all my holdings, Realty Income is my favorite. It provides me with reliable and growing dividend income, giving me true peace of mind as an income investor.
Matt DiLallo has positions in Realty Income. The Motley Fool has positions in and recommends Realty Income. The Motley Fool has a disclosure policy.
2025-11-08 22:271mo ago
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CRMT Investor News: If You Have Suffered Losses in America's Car-Mart, Inc. (NASDAQ: CRMT), You Are Encouraged to Contact The Rosen Law Firm About Your Rights
WHY: Rosen Law Firm, a global investor rights law firm, continues to investigate potential securities claims on behalf of shareholders of America’s Car-Mart, Inc. (NASDAQ: CRMT) resulting from allegations that America’s Car-Mart, Inc. may have issued materially misleading business information to the investing public.
SO WHAT: If you purchased America’s Car-Mart, Inc. securities you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement. The Rosen Law Firm is preparing a class action seeking recovery of investor losses.
WHAT TO DO NEXT: To join the prospective class action, go to https://rosenlegal.com/submit-form/?case_id=46025 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
WHAT IS THIS ABOUT: On September 4, 2025, during market hours, Benzinga published an article entitled “America’s Car-Mart Stock Plunges After Sales Volume Dip, Delinquency Uptick.” The article stated that America’s Car-Mart, Inc. stock was trading “lower after the company reported first-quarter results. The company reported a first-quarter loss of 69 cents per share, compared with a net loss of 15 cents per share in the year-ago period.”
On this news, America’s Car-Mart, Inc. stock fell 18.2% on September 4, 2025.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved, at that time, the largest ever securities class action settlement against a Chinese Company. At the time Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs’ Bar. Many of the firm’s attorneys have been recognized by Lawdragon and Super Lawyers.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
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Contact Information:
Laurence Rosen, Esq.
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The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
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Q3: 2025-11-06 Earnings SummaryEPS of $3.09 beats by $1.20
|
Revenue of
$115.46M
(122.85% Y/Y)
beats by $57.41M
Ligand Pharmaceuticals Incorporated (LGND) Q3 2025 Earnings Call November 6, 2025 8:30 AM EST
Company Participants
Melanie Herman
Todd Davis - CEO & Director
Lauren Hay
Octavio Espinoza - Chief Financial Officer
Conference Call Participants
Trevor Allred - Oppenheimer & Co. Inc., Research Division
Jayed Momin - Stifel, Nicolaus & Company, Incorporated, Research Division
Sahil Dhingra - RBC Capital Markets, Research Division
Presentation
Operator
Thank you for standing by. Welcome to Ligand Third Quarter 2025 Earnings Call. [Operator Instructions]
I would now like to turn the conference over to Melanie Herman. Please go ahead.
Melanie Herman
Good morning, everyone, and welcome to Ligand's Third Quarter 2025 Earnings Call. During the call today, we will review the financial results we released earlier today and provide commentary on our partner pipeline and business development activity, followed by a question-and-answer session.
Before we get started, I would like to point out that we will be discussing non-GAAP results, which excludes certain items such as stock-based compensation, amortization of intangible assets, amortization or impairment of financial assets, losses from derivative assets and gain from the sale of the Pelthos business, amongst others. I encourage you to review the reconciliation of these non-GAAP measures to their most directly comparable GAAP measures, which can be found in today's release available on our website.
We believe these adjusted measures provide valuable insight into our core operating performance, both historically and moving forward. Our earnings release and a link to today's webcast can be found in the Investor Relations section of our website at ligand.com. With me on the call today are CEO, Todd Davis; Chief Financial Officer, Tavo Espinoza; and Vice President of Strategic Planning and Investment Analytics, Lauren Hay.
This call is being recorded, and the audio portion will be archived in the Investors section of our website. On today's
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New Post Hoc Analysis from the HELIOS-B Phase 3 Study Shows Vutrisiran Improved Measures of Heart Structure and Function in Patients with ATTR-CM
− Analyses Presented at the American Heart Association Scientific Sessions 2025 Underscore Vutrisiran’s Differentiated Profile –
− Cardiovascular Magnetic Resonance (CMR) and Echocardiographic Analyses Demonstrate that Treatment with Vutrisiran Resulted in Significant Changes on Multiple Functional and Structural Cardiac Parameters –
– In a Cohort of HELIOS-B Patients, CMR Imaging Showed Amyloid Regression in 22% of Vutrisiran Treated Patients with No Regression Found in Patients Who Received Placebo –
– Treatment with Vutrisiran Preserved Kidney Function in HELIOS-B Patients, and Reduced Risk of Death and Cardiovascular Events in Patients with Advanced Chronic Kidney Disease –
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today announced results from new post hoc analyses of the HELIOS-B Phase 3 study of AMVUTTRA® (vutrisiran), an RNAi therapeutic approved for the treatment of the cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis (ATTR-CM) and the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN) in adults. Data from cardiovascular magnetic resonance (CMR) and echocardiographic imaging as well as renal function analyses were presented at the American Heart Association (AHA) Scientific Sessions 2025 in New Orleans, Louisiana.
As a multisystem disease, ATTR-CM can impact the health and function of organs throughout the body. These analyses evaluated the effect of vutrisiran on critical measures of heart function and structure as well as kidney health, providing deeper insight into its potential impact on key organs affected by the disease.
HELIOS-B Analyses: Cardiac Structure, Function, and Amyloid Burden
In ATTR-CM, amyloid deposits in the heart lead to thickening and stiffening of the ventricles, affecting how well the heart functions and increasing the risk of heart failure and death. Advanced imaging techniques offer insights into structural and functional changes, capturing the overall burden of amyloid deposits and their impact on cardiac function.
A CMR analysis evaluated a retrospectively identified cohort of HELIOS-B patients from the National Amyloidosis Centre in London who underwent serial CMR scans as part of their routine clinical care at baseline (N=43), Year 1 (N=39), Year 2 (N=26), and Year 3 (N=17).
A mixed model analysis that pooled 24- and 36-month data found that treatment with vutrisiran monotherapy was associated with nominally statistically significant and directionally favorable changes in multiple measures of cardiac structure, function, and amyloid burden, including improvements in left and right ventricular ejection fractions as well as stroke volumes and left ventricular mass, compared to placebo.
Treatment with vutrisiran also reduced extracellular volume (ECV), which is thought to reflect amyloid buildup in the heart. At Year 3, amyloid regression, as assessed by ECV, was observed in 22% of patients treated with vutrisiran, while no patients who received placebo showed regression; conversely, progression occurred in 63% of patients who received placebo compared to 11% of patients treated with vutrisiran.
At Year 3, patients treated with vutrisiran exhibited an absolute mean (standard deviation) reduction in ECV of -0.10% (± 4.72) versus an increase of 7.86% (± 5.67) in the placebo group (p=0.006).
To further assess cardiac function in patients with ATTR-CM, echocardiographic parameters including left atrial strain (LAS) and right ventricular free wall strain (RVFWS) were evaluated in analyses of the overall HELIOS-B population.
The LAS analysis demonstrated that measures of LAS were associated with baseline disease severity, mortality, and cardiovascular (CV) events, and that patients treated with vutrisiran experienced less worsening in LAS at 30 months, compared to those receiving placebo.
The RVFWS analysis showed that worse RVFWS was associated with higher risk of adverse outcomes and that treatment with vutrisiran stabilized RVFWS at 30 months, compared to placebo.
“As ATTR-CM progressively damages the heart muscle, making it thicker, stiffer, and less capable of pumping blood effectively, patients experience worsening symptoms, quality of life, and outcomes,” said Marianna Fontana, M.D., Ph.D., HELIOS-B investigator, Professor of Cardiology, University College London, National Amyloidosis Center, Royal Free Hospital, London. “The HELIOS-B CMR analysis provides compelling initial evidence that treatment with vutrisiran can counteract these changes in some patients, as shown by favorable impacts on measures of cardiac structure and function as well as regression of amyloid burden. These results suggest that vutrisiran has the potential not only to slow disease progression, but to reverse some of the structural damage caused by amyloid deposition in the heart in some patients.”
HELIOS-B Analysis: Renal Function and CV Outcomes in Patients with Severe Chronic Kidney Disease (CKD)
Kidney involvement is common in patients with ATTR-CM and is associated with disease progression along with worse patient outcomes as amyloid deposits in the kidneys can lead to a decline in kidney function, indicated by a decreasing estimated glomerular filtration rate (eGFR).
A post hoc analysis of the HELIOS-B study evaluated the impact of vutrisiran on renal function and assessed the efficacy and safety of vutrisiran in patients who advanced to severe CKD during the double-blind period. Outcomes, including the composite endpoint of all-cause mortality (ACM) and recurrent CV events, as well as safety, were assessed in patients who advanced to CKD Stage 4 or greater (eGFR < 30 mL/min/1.73 m²) in the overall population, vutrisiran monotherapy population, and baseline tafamidis treatment group.
In the overall population, treatment with vutrisiran resulted in fewer patients experiencing ≥40% decreases in eGFR from baseline during the double-blind period, compared to placebo (12.7% vs 21.2%).
In patients in the overall population who progressed to CKD Stage 4 or greater during the double-blind period, treatment with vutrisiran reduced the risk of ACM and CV events (hazard ratio [HR] 0.47; 95% confidence interval [CI]: 0.26–0.85), compared to placebo.
In both analyses, results observed in patients who progressed to CKD Stage 4 or greater were consistent across the overall population, vutrisiran monotherapy, and baseline tafamidis treatment groups, and were also consistent with vutrisiran’s established efficacy profile from the primary HELIOS-B analysis.
The safety profile of vutrisiran in patients who advanced to CKD Stage 4 or greater was comparable with that established in the overall population of the HELIOS-B study.
“The new HELIOS-B analyses add depth to the growing body of evidence supporting AMVUTTRA’s first-line potential in ATTR-CM treatment,” said John Vest, M.D., Senior Vice President, TTR Global Clinical Lead, Alnylam. “From heart structure and function to renal health, the benefits observed are consistent across a wide range of measures and analyses, underscoring the potential for protection of the multiple organs impacted by this systemic disease. These findings build on the broadening dataset from HELIOS-B and continue to support the potential of AMVUTTRA to provide meaningful clinical benefit for patients living with this rapidly progressive multisystem disease.”
Data from the HELIOS-B study supported the approvals of AMVUTTRA for the treatment of the cardiomyopathy of wild-type or hereditary ATTR-CM in adults in the United States (US), Brazil, European Union (EU), Japan, United Arab Emirates (UAE), United Kingdom (UK), and Switzerland. AMVUTTRA is an RNAi therapeutic that works upstream to deliver rapid knockdown of transthyretin, addressing the disease at its source, with four subcutaneous doses per year. Collectively, AMVUTTRA has more than 8,000 patient-years of experience worldwide and is the first RNAi therapeutic approved for the treatment of both ATTR-CM and hATTR-PN in adults.
For additional information on Alnylam’s presentations in ATTR-CM at the AHA 2025 Scientific Sessions, please visit Capella.
Indications and Important Safety Information
Indications Approved by the U.S. FDA
AMVUTTRA® (vutrisiran) is indicated for the treatment of the:
cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular mortality, cardiovascular hospitalizations and urgent heart failure visits.
polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN) in adults.
Important Safety Information
Reduced Serum Vitamin A Levels and Recommended Supplementation
AMVUTTRA treatment leads to a decrease in serum vitamin A levels.
Supplementation at the recommended daily allowance (RDA) of vitamin A is advised for patients taking AMVUTTRA. Higher doses than the RDA should not be given to try to achieve normal serum vitamin A levels during treatment with AMVUTTRA, as serum vitamin A levels do not reflect the total vitamin A in the body.
Patients should be referred to an ophthalmologist if they develop ocular symptoms suggestive of vitamin A deficiency (e.g., night blindness).
Adverse Reactions
In a study of patients with hATTR-PN, the most common adverse reactions that occurred in patients treated with AMVUTTRA were pain in extremity (15%), arthralgia (11%), dyspnea (7%), and vitamin A decreased (7%).
In a study of patients with ATTR-CM, no new safety issues were identified.
For additional information about AMVUTTRA, please see the full U.S. Prescribing Information (revised March 2025)
About AMVUTTRA
AMVUTTRA® (vutrisiran) is an RNAi therapeutic that delivers rapid knockdown of transthyretin (TTR), addressing the underlying cause of transthyretin (ATTR) amyloidosis. It is marketed in more than 15 countries for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN) in adults and it is also approved for the treatment of the cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis (ATTR-CM) in adults in the US, EU, UK, Brazil, Japan, Switzerland, and UAE. In a clinical study, AMVUTTRA rapidly knocked down TTR in as early as six weeks and decreased TTR levels by 87% with two and a half years of treatment. Administered quarterly via subcutaneous injection, AMVUTTRA is the first and only RNAi therapeutic approved for the treatment of both the cardiomyopathy manifestations of ATTR amyloidosis and the polyneuropathy manifestations of hereditary transthyretin-mediated amyloidosis (hATTR).
About ATTR
Transthyretin amyloidosis (ATTR) is an underdiagnosed, rapidly progressive, debilitating and fatal disease caused by misfolded transthyretin (TTR) proteins, which accumulate as amyloid deposits in various parts of the body, including the nerves, heart, and gastrointestinal tract. Patients may present with polyneuropathy, cardiomyopathy, or both manifestations of disease. There are two different forms of ATTR – hereditary ATTR (hATTR), which is caused by a TTR gene variant and affects approximately 50,000 people worldwide, and wild-type ATTR (wtATTR), which occurs without a TTR gene variant and impacts an estimated 200,000 – 300,000 people worldwide.1-4
About RNAi
RNAi (RNA interference) is a natural cellular process of gene silencing that represents one of the most promising and rapidly advancing frontiers in biology and drug development today.5 Its discovery has been heralded as “a major scientific breakthrough that happens once every decade or so,” and was recognized with the award of the 2006 Nobel Prize for Physiology or Medicine.6 By harnessing the natural biological process of RNAi occurring in our cells, a new class of medicines known as RNAi therapeutics is now a reality. Small interfering RNA (siRNA), the molecules that mediate RNAi and comprise Alnylam’s RNAi therapeutic platform, function upstream of today’s medicines by potently silencing messenger RNA (mRNA) – the genetic precursors – that encode for disease-causing or disease pathway proteins, thus preventing them from being made.5 This is a revolutionary approach with the potential to transform the care of patients with genetic and other diseases.
About Alnylam Pharmaceuticals
Alnylam (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and prevalent diseases with unmet need. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach yielding transformative medicines. Since its founding in 2002, Alnylam has led the RNAi Revolution and continues to deliver on a bold vision to turn scientific possibility into reality. Alnylam’s commercial RNAi therapeutic products include AMVUTTRA® (vutrisiran), ONPATTRO® (patisiran), GIVLAARI® (givosiran), and OXLUMO® (lumasiran), which are being developed and commercialized by Alnylam, and Leqvio® (inclisiran) and Qfitlia™ (fitusiran), which are being developed and commercialized by Alnylam’s partners, Novartis and Sanofi, respectively. Alnylam has a deep pipeline of investigational medicines, including multiple product candidates that are in late-stage development. Alnylam is executing on its “Alnylam P5x25” strategy to deliver transformative medicines in both rare and common diseases benefiting patients around the world through sustainable innovation and exceptional financial performance, resulting in a leading biotech profile. Alnylam is headquartered in Cambridge, MA. For more information about our people, science and pipeline, please visit www.alnylam.com and engage with us on X (formerly Twitter) at @Alnylam, or on LinkedIn, Facebook, or Instagram.
Alnylam Forward-Looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. All statements other than historical statements of fact regarding Alnylam’s expectations, beliefs, goals, plans or prospects including, without limitation, Alnylam’s expectations regarding the safety and efficacy of vutrisiran as a treatment for ATTR-CM, including vutrisiran’s impact on measures of cardiac structure and function; the potential for treatment with AMVUTTRA to result in regression of amyloid burden in some patients; the potential of AMVUTTRA to slow disease progression and to reverse some of the structural damage caused by amyloid deposition in the heart in some patients; the potential impact of vutrisiran on key organs affected by ATTR-CM; AMVUTTRA’s potential to be a first-line treatment for ATTR-CM; AMVUTTRA’s potential to protect multiple organs impacted by ATTR-CM and to deliver meaningful clinical benefit for patients living with ATTR-CM; and Alnylam’s ability to execute on its “Alnylam P5x25” strategy to deliver transformative medicines in both rare and common diseases benefiting patients around the world through sustainable innovation and exceptional financial performance, resulting in a leading biotech profile should be considered forward-looking statements. Actual results and future plans may differ materially from those indicated by these forward-looking statements as a result of various important risks, uncertainties and other factors, including, without limitation, risks and uncertainties relating to Alnylam’s ability to successfully execute on its “Alnylam P5x25” strategy; Alnylam’s ability to discover and develop novel drug candidates and delivery approaches and successfully demonstrate the efficacy and safety of its product candidates; the pre-clinical and clinical results for Alnylam’s product candidates; the possibility of unfavorable new clinical data and further analyses of existing clinical data; interim and preliminary data; the possibility that clinical data are subject to differing interpretations and assessments by regulatory agencies; actions or advice of regulatory agencies and Alnylam’s ability to obtain and maintain regulatory approval for its product candidates, as well as favorable pricing and reimbursement; successfully launching, marketing and selling Alnylam’s approved products globally; delays, interruptions or failures in the manufacture and supply of Alnylam’s product candidates or its marketed products; obtaining, maintaining and protecting intellectual property; Alnylam’s ability to manage its growth and operating expenses through disciplined investment in operations and its ability to achieve a self-sustainable financial profile in the future; Alnylam’s ability to maintain strategic business collaborations; Alnylam’s dependence on third parties for the development and commercialization of certain products; the outcome of litigation; the potential risk of future government investigations; and unexpected expenditures; as well as those risks more fully discussed in the “Risk Factors” filed with Alnylam’s 2024 Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC), as may be updated from time to time in Alnylam’s subsequent Quarterly Reports on Form 10-Q, and in other filings that Alnylam makes with the SEC. In addition, any forward-looking statements represent Alnylam’s views only as of today and should not be relied upon as representing Alnylam’s views as of any subsequent date. Alnylam explicitly disclaims any obligation, except to the extent required by law, to update any forward-looking statements.
References
1 Hawkins PN, Ando Y, Dispenzeri A, et al. Ann Med. 2015;47(8):625-638.
2 Gertz MA. Am J Manag Care. 2017;23(7):S107-S112.
3 Conceicao I, Gonzalez-Duarte A, Obici L, et al. J Peripher Nerv Syst. 2016;21:5-9.
4 Ando Y, Coelho T, Berk JL, et al. Orphanet J Rare Dis. 2013;8:31.
November 08, 2025 5:01 PM EST | Source: The Rosen Law Firm PA
New York, New York--(Newsfile Corp. - November 8, 2025) - WHY: Rosen Law Firm, a global investor rights law firm, announces a class action lawsuit on behalf of purchasers and acquirers of Synopsys, Inc. (NASDAQ: SNPS) securities between December 4, 2024 and September 9, 2025, both dates inclusive (the "Class Period"). A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than December 30, 2025.
SO WHAT: If you purchased Synopsys securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
WHAT TO DO NEXT: To join the Synopsys class action, go to https://rosenlegal.com/submit-form/?case_id=44981 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than December 30, 2025. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
WHY ROSEN LAW: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Many of these firms do not actually litigate securities class actions. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved, at that time, the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs' Bar. Many of the firm's attorneys have been recognized by Lawdragon and Super Lawyers.
DETAILS OF THE CASE: According to the lawsuit, defendants throughout the Class Period made materially false and/or misleading statements, as well as failed to disclose material adverse facts about the Company's business, operations, and prospects. Specifically, defendants failed to disclose to investors: (1) the extent to which Synopsys' increased focus on artificial intelligence customers, which require additional customization, was deteriorating the economics of its Design IP business; (2) that, as a result, "certain road map and resource decisions" were unlikely to "yield their intended results,"; (3) that the foregoing had a material negative impact on financial results; and (4) as a result of the foregoing, defendants' positive statements about Synopsys' business, operations, and prospects were materially misleading and/or lacked a reasonable basis. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the Synopsys class action, go to https://rosenlegal.com/submit-form/?case_id=44981 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor's ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
-------------------------------
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/273705
2025-11-08 22:271mo ago
2025-11-08 17:061mo ago
INSP Investors Have Opportunity to Lead Inspire Medical Systems, Inc. Securities Fraud Lawsuit
Why: Rosen Law Firm, a global investor rights law firm, announces a class action lawsuit on behalf of purchasers of common stock of Inspire Medical Systems, Inc. (NYSE: INSP) between August 6, 2024 and August 4, 2025, both dates inclusive (the "Class Period"). A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than January 5, 2026.
So what: If you purchased Inspire Medical common stock during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement.
What to do next: To join the Inspire Medical class action, go to https://rosenlegal.com/submit-form/?case_id=21452 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action. A class action lawsuit has already been filed. If you wish to serve as lead plaintiff, you must move the Court no later than January 5, 2026. A lead plaintiff is a representative party acting on behalf of other class members in directing the litigation.
Why Rosen Law: We encourage investors to select qualified counsel with a track record of success in leadership roles. Often, firms issuing notices do not have comparable experience, resources, or any meaningful peer recognition. Be wise in selecting counsel. The Rosen Law Firm represents investors throughout the globe, concentrating its practice in securities class actions and shareholder derivative litigation. Rosen Law Firm has achieved, at that time, the largest ever securities class action settlement against a Chinese Company. Rosen Law Firm was Ranked No. 1 by ISS Securities Class Action Services for number of securities class action settlements in 2017. The firm has been ranked in the top 4 each year since 2013 and has recovered hundreds of millions of dollars for investors. In 2019 alone the firm secured over $438 million for investors. In 2020, founding partner Laurence Rosen was named by law360 as a Titan of Plaintiffs' Bar. Many of the firm's attorneys have been recognized by Lawdragon and Super Lawyers.
Details of the case: According to the lawsuit, throughout the Class Period, defendants misrepresented and failed to disclose key facts about Inspire V, a sleep apnea device, including the actual market demand for the device and whether Inspire Medical had taken the steps necessary to launch it. Defendants issued a series of materially false and misleading statements that led investors to believe that demand for Inspire V was strong and that Inspire Medical had taken the necessary steps for a successful launch. When the true details entered the market, the lawsuit claims that investors suffered damages.
To join the Inspire Medical class action, go to https://rosenlegal.com/submit-form/?case_id=21452 or call Phillip Kim, Esq. toll-free at 866-767-3653 or email [email protected] for information on the class action.
No Class Has Been Certified. Until a class is certified, you are not represented by counsel unless you retain one. You may select counsel of your choice. You may also remain an absent class member and do nothing at this point. An investor's ability to share in any potential future recovery is not dependent upon serving as lead plaintiff.
Follow us for updates on LinkedIn: https://www.linkedin.com/company/the-rosen-law-firm, on Twitter: https://twitter.com/rosen_firm or on Facebook: https://www.facebook.com/rosenlawfirm/.
Attorney Advertising. Prior results do not guarantee a similar outcome.
Contact Information:
Laurence Rosen, Esq.
Phillip Kim, Esq.
The Rosen Law Firm, P.A.
275 Madison Avenue, 40th Floor
New York, NY 10016
Tel: (212) 686-1060
Toll Free: (866) 767-3653
Fax: (212) 202-3827
[email protected]
www.rosenlegal.com
SOURCE THE ROSEN LAW FIRM, P. A.
2025-11-08 22:271mo ago
2025-11-08 17:131mo ago
Intellia Therapeutics Presents Positive Pooled Phase 1/2 Data of Lonvoguran Ziclumeran (lonvo-z) in Patients with Hereditary Angioedema
Deep, stable and durable reductions in kallikrein observed Among 32 patients who received a 50 mg dose of lonvo-z as of data cutoff: 31 (97%) were attack-free and long-term prophylaxis (LTP)-free 24 (75%) were attack-free and LTP-free for at least seven months (up to 32 months)Among the 11 patients who originally received a 50 mg dose in Phase 2, 10 were attack-free and LTP-free Continue to observe a well-tolerated safety profile with up to three years of patient follow-up and no new long-term risks identified CAMBRIDGE, Mass., Nov. 08, 2025 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (NASDAQ: NTLA), a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies, today presented positive clinical data from a pooled analysis of all patients who received a 50 milligram (mg) dose of lonvo-z in the company’s ongoing Phase 1/2 clinical trial in patients with hereditary angioedema (HAE). These results were shared in an oral presentation today at the American College of Allergy, Asthma & Immunology (ACAAI) 2025 Annual Scientific Meeting in Orlando, Florida.
“Today’s data further support our belief that lonvo-z could completely redefine the HAE treatment landscape,” said Intellia President and Chief Executive Officer John Leonard, M.D. “With up to three years of follow-up, the vast majority of patients who received a one-time 50 mg dose of lonvo-z – including 10 of our original 11 patients who received this dose in Phase 2 – were both attack-free and LTP-free as of the data cutoff. We are looking forward to our approaching topline readout from our Phase 3 HAELO clinical trial by mid-2026.”
“Hereditary angioedema is a condition with significant burden that is marked by the unpredictable nature of when the next attack could occur, the painful and often prolonged swellings themselves as well as the need for lifelong treatment,” said Dr. Danny Cohn, M.D., Ph.D., Internist, Department of Vascular Medicine, Amsterdam University Medical Center. “The data presented today offer hope that lonvo-z could significantly reduce or remove those burdens for many patients via a one-time treatment. I am eagerly awaiting results from the ongoing HAELO Phase 3 clinical trial.”
Pooled Phase 1/2 Analysis
Intellia’s global Phase 1/2 clinical trial is evaluating the safety, tolerability, pharmacokinetics and pharmacodynamics of lonvo-z in adults with HAE Types I or II. Today’s presentation was based on a pooled analysis of all 32 patients who have received a one-time 50 mg treatment of lonvo-z via intravenous infusion in the Phase 1/2 trial. Of the 32 patients, 15 had initially received the 50 mg dose at study Day 1 (four in Phase 1 and 11 in Phase 2) and 17 were treated after unblinding of the Phase 2 clinical trial for the primary analysis (11 had originally received a 25 mg dose of lonvo-z, which was determined to be a suboptimal dose, and six had previously received placebo). The data cut-off for the analysis was August 29, 2025.
Deep, stable and durable reductions in plasma kallikrein were observed in all patients, with a mean reduction of 89% at month 24. Among the 32 patients, 31 (97%) were both attack-free and LTP-free as of the data cutoff, with 24 (75%) being attack-free and LTP-free for at least seven months (up to 32 months for patients with the longest follow-up). Of the 11 patients who initially received the 50 mg dose of lonvo-z in Phase 2, 10 were attack-free and LTP-free (nine for 7-32 months and one for <6 months). The one patient who was not attack-free and LTP-free as of the data cutoff had a 59% reduction from baseline in their monthly attack rate.
Safety
After a 50 mg dose, a well-tolerated safety profile was observed for up to three years of follow-up with no long-term risks identified. The most frequent treatment-emergent adverse events (TEAEs) within 28 days of infusion were infusion-related reactions, fatigue and headache. The most frequent TEAEs reported ≥28 days after infusion up to long-term follow-up (LTFU) were nasopharyngitis, upper respiratory tract infection, back pain, arthralgia and COVID-19. A single Grade 2 AST elevation was reported among all patients who received a 50 mg dose of lonvo-z. This event had an onset at Day 1 and spontaneously resolved by Day 4 in a patient previously treated with lonvo-z 25 mg. Safety of the 50 mg dose after patients received the suboptimal dose (25 mg) was consistent with the overall clinical trial population. There were no clinically significant shifts in liver enzymes or coagulation parameters. One serious adverse event (SAE), a pulmonary embolism, was observed in a patient with multiple risk factors one year after the infusion, and the event resolved without sequelae. In LTFU (n=17), there were no SAEs or TEAEs reported with 50 mg of lonvo-z, as of the data cutoff.
A one-time 50 mg treatment of lonvo-z is being further evaluated in patients with HAE in the ongoing global Phase 3 HAELO clinical trial that completed enrollment in September 2025.
The ACAAI data presentation will be available on the Scientific Publications & Presentations section of intelliatx.com.
About the Lonvoguran Ziclumeran (lonvo-z, formerly known as NTLA-2002) Clinical Program
Intellia’s ongoing Phase 1/2 clinical trial is evaluating the safety and efficacy of lonvo-z in adults with Type I or Type II hereditary angioedema (HAE). The Phase 1 portion is an international, open-label trial designed to identify the dose level of lonvo-z selected for further evaluation in the Phase 2 portion of the trial. Enrollment in both portions of the Phase 1/2 trial is complete. Intellia completed enrollment in the global Phase 3, randomized, double-blind, placebo-controlled HAELO clinical trial in September of 2025. Visit clinicaltrials.gov (NCT05120830) for more details.
About Lonvo-z
Based on Nobel Prize-winning CRISPR/Cas9 technology, lonvo-z has the potential to become the first one-time treatment for hereditary angioedema (HAE). Lonvo-z is an investigational in vivo CRISPR-based gene editing therapy that is currently being investigated in HAELO, a Phase 3 clinical trial in HAE, and is designed to prevent HAE attacks by inactivating the kallikrein B1 (KLKB1) gene, which encodes for prekallikrein, the kallikrein precursor protein. Interim Phase 1/2 clinical data showed dramatic reductions in attack rate, as well as consistent, deep and durable reductions in kallikrein levels. Lonvo-z has received five notable regulatory designations, including Orphan Drug and RMAT Designation by the U.S. Food and Drug Administration (FDA), the Innovation Passport by the U.K. Medicines and Healthcare products Regulatory Agency (MHRA), Priority Medicines (PRIME) Designation by the European Medicines Agency, as well as Orphan Drug Designation (ODD) by the European Commission.
About Intellia Therapeutics
Intellia Therapeutics, Inc. (NASDAQ:NTLA) is a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies. Since its inception, Intellia has focused on leveraging gene editing technology to develop novel, first-in-class medicines that address important unmet medical needs and advance the treatment paradigm for patients. Intellia’s deep scientific, technical and clinical development experience, along with its people, is helping set the standard for a new class of medicine. To harness the full potential of gene editing, Intellia continues to expand the capabilities of its CRISPR-based platform with novel editing and delivery technologies. Learn more at intelliatx.com and follow us @intelliatx.
Forward-Looking Statements
This press release contains “forward-looking statements” of Intellia Therapeutics, Inc. (“Intellia” or the “Company”) within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements regarding Intellia’s beliefs and expectations concerning: the safety, efficacy, success and advancement of its clinical programs for lonvoguran ziclumeran or “lonvo-z” (f/k/a NTLA-2002) for hereditary angioedema (“HAE”), including the ability to successfully complete its global Phase 3 HAELO study and to present a topline data readout from the HAELO study by mid-2026; and lonvo-z’s potential to significantly reduce or remove burdens for patients with HAE and to become the first one-time treatment for HAE.
Any forward-looking statements in this press release are based on management’s current expectations and beliefs of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: risks related to Intellia’s ability to protect and maintain its intellectual property position; risks related to Intellia’s relationship with third parties, including its contract manufacturers, licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; risks related to Intellia’s ability to protect and maintain its intellectual property position; risks related to valid third party intellectual property; risks related to Intellia’s relationship with third parties, including its licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; uncertainties related to regulatory agencies’ evaluation of regulatory filings and other information related to our product candidates, including lonvo-z; uncertainties related to the authorization, initiation and conduct of studies and other development requirements for our product candidates, including uncertainties related to regulatory approvals to conduct clinical trials, including our ability to complete the Phase 3 HAELO study for HAE, present a topline data readout from the HAELO study by mid-2026, and generate data to support lonvo-z’s potential to significantly reduce or remove burdens for patients with HAE via a one-time treatment; the risk that any one or more of Intellia’s product candidates, including lonvo-z, will not be successfully developed and commercialized; and the risk that the results of preclinical studies or clinical studies will not be predictive of future results in connection with future studies for the same product candidate or Intellia’s other product candidates. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Intellia’s most recent annual report of Form 10-K and quarterly report on Form 10-Q, as well as discussions of potential risks, uncertainties, and other important factors in Intellia’s other filings with the Securities and Exchange Commission. All information in this press release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law.
Intellia Contacts:
Investors:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc. [email protected]
Vertex Presents Updated Phase 1/2 Data From RUBY-3 Study That Continue to Demonstrate Best-in-Class Potential for Povetacicept in Adults with IgA Nephropathy and Primary Membranous Nephropathy at American Society of Nephrology Kidney Week
BOSTON--(BUSINESS WIRE)--Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced updated data for povetacicept (pove) in IgA nephropathy (IgAN) and primary membranous nephropathy (pMN) from the ongoing RUBY-3 trial at the American Society of Nephrology (ASN) Kidney Week 2025 in Houston, Texas. Pove is an investigational recombinant fusion protein therapeutic and dual inhibitor of the BAFF (B cell activating factor) and APRIL (a proliferation inducing ligand) cytokines. Pove is the on.
2025-11-08 21:271mo ago
2025-11-08 13:011mo ago
Exploring Ripple's strategic sidestep from Wall Street spotlight
In August 2025, Ripple Labs formally closed its years-long battle with the Securities and Exchange Commission (SEC).
The company paid a $125 million civil penalty, accepted an injunction on certain institutional XRP sales, and walked away with something more valuable than victory: clarity.
Judge Analisa Torres had already ruled in July 2023 that XRP itself wasn’t inherently a security and that programmatic sales on exchanges didn’t trigger Howey test requirements.
Direct institutional sales totaling about $728 million did violate securities law, but the core business survived intact.
The existential threat evaporated, and the stain of “unregistered security in secondary markets” lifted.
Industry watchers expected the obvious next move: an initial public offering to capitalize on vindication, access deeper pools of capital, and cement Ripple’s status as a legitimate financial infrastructure company.
Instead, Ripple did something else.
It raised half a billion dollars at a $40 billion valuation from Fortress Investment Group and Citadel Securities, executed a $1 billion tender offer at the same price to provide early investor liquidity, acquired a prime broker for $1.25 billion, launched a stablecoin, and applied for a US national bank charter.
The firm did everything except go public.
That choice deserves scrutiny not because it suggests weakness, since the company’s moves demonstrate the opposite, but because it reveals how crypto’s most sophisticated operators read the actual state of US public markets.
Ripple’s hesitation is less about what it can’t do and more about what it has learned watching others try.
Capital without the theaterThe traditional case for an IPO rests on two pillars: access to capital and liquidity for stakeholders, and Ripple solved both without filing an S-1.
The 2025 capital raise attracted investors such as Fortress, Citadel Securities, Brevan Howard, Marshall Wace, Pantera Capital, and Galaxy Digital. This is the kind of investor roster that typically signals institutional legitimacy.
These aren’t crypto-native venture funds taking flyers on protocols, but multi-strategy macro shops and market makers deploying significant capital at a $40 billion valuation.
The tender offer provided exit liquidity for early employees and investors without the roadshow circus or quarterly earnings calls.
New strategic backers secured positions, while Ripple preserved tight control over its XRP treasury and RLUSD stablecoin economics.
Additionally, the company effectively recreated most benefits of a public listing while remaining in a private disclosure regime that doesn’t require explaining every strategic decision to retail shareholders and activist investors.
When a private round led by Citadel Securities functions as a de facto institutional seal of approval, the signaling value of a Wall Street listing loses some of its historical premium.
In other words, Ripple doesn’t need the Nasdaq to prove it’s real, it already proved that by attracting capital from firms that trade hundreds of billions in traditional securities daily.
The XRP machine under glassGoing public would force uncomfortable transparency around questions that equity analysts ask reflexively, but token projects prefer to keep blurry.
How much of Ripple’s revenue and cash flow depends on selling XRP over time? How should investors value a company controlling a large escrowed stash of a volatile token that it partially influences through its own product decisions and announcements? How durable is growth in RLUSD, payment processing, custody services, and prime brokerage compared to XRP mark-to-market effects?
These aren’t hypothetical concerns. A 2024 Forbes analysis characterized Ripple as a “crypto zombie” with modest fee income relative to enormous token holdings.
The company has since moved aggressively to fix that characterization through the $1.25 billion Hidden Road acquisition, the $200 million purchase of stablecoin infrastructure firm Rail, and the buildout of RLUSD, which processes about $95 billion in payments.
But an IPO would freeze that evolution into SEC filings, inviting constant comparison between operating business fundamentals and token treasury fluctuations.
Ripple also carries a permanent federal injunction tied to institutional XRP sales and a fresh $125 million violation on its books. That history is absolutely IPO-manageable, as plenty of companies list with regulatory settlements behind them, but it’s not clean.
It means extra risk-factor disclosures, extra analyst questions, and a real-time reminder that US securities law has already embedded itself in the company’s past behavior.
A firm that spent years arguing XRP isn’t a security understandably has limited enthusiasm for immediately becoming a registered securities issuer, whose every XRP movement would be judged by the same rulebook.
Crypto’s public market scar tissueRipple’s caution makes more sense in the context of how US public markets have treated crypto companies that did take the leap.
Coinbase is the cautionary tale. It executed a textbook direct listing in April 2021, complete with blue-chip advisors and full regulatory disclosure.
Within two years, the SEC sued Coinbase anyway, alleging it operated an unregistered exchange and broker-dealer.
The lesson absorbed across the industry: going public is not a regulatory safe harbor. It can paint a bigger target on your back by centralizing liability and creating a highly visible enforcement trophy.
Circle attempted a SPAC merger in 2021, but it was killed when regulatory tone and market conditions soured. The company finally completed a successful IPO in 2025.
Gemini followed a similar path, listing after regulatory frameworks solidified. Crypto firms that list cleanly are those whose economics resemble those of traditional, boring, fee-and-yield fintechs.
Companies that resemble regulated money transmitters or custody providers can fit into existing analyst models and compliance frameworks.
Ripple doesn’t fit those boxes. It’s simultaneously a token issuer with XRP, a would-be bank with a charter application pending, a stablecoin operator with RLUSD, a capital markets infrastructure owner with Hidden Road, and a firm with a documented enforcement history.
Cramming that hybrid structure into one public ticker invites every regulatory constituency to fight over how the company should be policed, priced, and potentially broken apart.
Maintaining privacy while pursuing a national bank charter and establishing structured relationships with multiple regulators enables Ripple to select its referees.
The bank charter route subjects the firm to prudential supervision, but treats RLUSD reserves parked at the Federal Reserve as banking activity, rather than securities issuance.
That’s a fundamentally different regulatory posture than trying to explain XRP custody and RLUSD mechanics in a Form 10-K while defending against potential securities litigation.
What hesitation revealsRipple’s “no rush” posture toward public markets is a signal worth decoding.
If a legally vindicated, strategically positioned, $40 billion-valued company backed by Citadel Securities, Fortress, and Brevan Howard still prefers tender offers, private rounds, and a bank charter application over a public listing, it’s not because the balance sheet is weak or the business model is broken.
Although much has changed during President Donald Trump’s administration, the US public market regime still treats crypto-native structures as problems to be contained rather than forms to be accommodated.
Despite years of maturation, institutional adoption, and regulatory battles fought to conclusion, the infrastructure for reasonably pricing and governing hybrid token-plus-operating-business companies remains underdeveloped.
Crypto firms have discovered they can now access deep institutional capital, regulatory legitimacy, and stakeholder liquidity through private placements, stablecoin frameworks like the GENIUS Act, and banking charters without surrendering narrative control or expanding their litigation surface area through public filings.
That’s not a temporary arbitrage. It’s a structural judgment about where the path of least resistance actually runs.
For Ripple specifically, staying private preserves maximum flexibility over XRP treasury management and RLUSD strategy while the company rebuilds itself as a full-stack financial infrastructure provider.
Listing now would lock that evolving story into quarterly earnings theater, which has historically not been kind to this industry.
Better to prove the model works, deepen regulatory relationships through the bank charter process, and wait until public markets can actually price what Ripple is becoming rather than what it used to be.
The company beat the SEC in court, but it’s choosing not to test whether Wall Street is ready to understand what comes next.
Mentioned in this article
2025-11-08 21:271mo ago
2025-11-08 13:171mo ago
Renowned Short-Seller James Chanos Closes Short Against Strategy as Bitcoin Premium Narrows
Short-seller James Chanos has closed his short position against Strategy after the firm's premium over its bitcoin holdings shrank, validating his bearish thesis.
2025-11-08 21:271mo ago
2025-11-08 13:371mo ago
HBAR Price Continues To Survive, Holds Above Month-Long Support
Hedera (HBAR) trades at $0.174, holding above the month-long $0.162 support despite persistent bearish pressure and weak overall market sentiment.The Chaikin Money Flow remains below zero, signaling continued outflows, while the RSI under 50.0 confirms limited buying strength and fading momentum.If inflows improve and HBAR reclaims $0.175 as support, it could rally toward $0.194–$0.200; otherwise, consolidation above $0.162 may persist.Hedera’s native token, HBAR, has shown remarkable resilience despite enduring repeated market crashes and failed recovery attempts.
The altcoin continues to hold above a key support level, maintaining investor confidence even as bearish market sentiment persists. However, questions remain about how long HBAR can sustain this stability.
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Hedera Needs Stronger Market SupportThe Chaikin Money Flow (CMF) indicator shows HBAR sitting in the bearish zone below the zero line, reflecting ongoing outflows. Although there has been a modest uptick recently, inflows are still insufficient to reverse the trend. This suggests that sellers maintain control of the market.
Until consistent inflows surpass outflows, the HBAR price will likely remain under pressure. The gradual increase in inflows indicates that investor interest is slowly returning, but it is not yet strong enough to dictate price direction.
Want more token insights like this? Sign up for Editor Harsh Notariya’s Daily Crypto Newsletter here.
HBAR CMF. Source: TradingViewThe Relative Strength Index (RSI) reinforces this bearish sentiment. Currently positioned below the neutral 50.0 mark, the RSI signals that market conditions are not favorable for recovery.
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The lack of upward momentum reflects broader market weakness and hesitancy among traders to re-enter bullish positions.
This bearish momentum poses a challenge for HBAR’s price performance. Without support from the overall market, any potential bounce could be limited or short-lived. For HBAR to regain strength, the RSI must rise toward neutral levels.
HBAR RSI. Source: TradingViewHBAR Price May Remain ConsolidatedHBAR is trading at $0.174 at the time of writing, hovering just below the $0.175 resistance level. Despite several setbacks, the token has managed to hold above its critical $0.162 support level, showcasing its resilience.
This support has been pivotal for HBAR over the past month, preventing a deeper decline toward $0.154. Even under current bearish conditions, the token will likely continue consolidating above this zone, providing a stable base for potential recovery.
HBAR Price Analysis. Source: TradingViewIf broader market conditions improve and inflows strengthen, HBAR could flip the $0.175 resistance into support. This could trigger a rally toward $0.194, paving the way for another attempt to breach $0.200 and potentially invalidate the bearish thesis.
Disclaimer
In line with the Trust Project guidelines, this price analysis article is for informational purposes only and should not be considered financial or investment advice. BeInCrypto is committed to accurate, unbiased reporting, but market conditions are subject to change without notice. Always conduct your own research and consult with a professional before making any financial decisions. Please note that our Terms and Conditions, Privacy Policy, and Disclaimers have been updated.
2025-11-08 21:271mo ago
2025-11-08 13:481mo ago
Bitcoin's 365-Day Moving Average Faces Breakdown Risk
The cryptocurrency market is once again under pressure, with Bitcoin (BTC) struggling to hold above critical support levels. After a brief recovery in October, BTC has slipped nearly 6% over the past week, according to CoinGecko data.
2025-11-08 21:271mo ago
2025-11-08 13:531mo ago
U.S. spot bitcoin ETFs see largest daily outflow since August as BTC price hovers around $100,000
CoinGape has covered the cryptocurrency industry since 2017, aiming to provide informative insights to our readers. Our journal analysts bring years of experience in market analysis and blockchain technology to ensure factual accuracy and balanced reporting. By following our Editorial Policy, our writers verify every source, fact-check each story, rely on reputable sources, and attribute quotes and media correctly. We also follow a rigorous Review Methodology when evaluating exchanges and tools. From emerging blockchain projects and coin launches to industry events and technical developments, we cover all facets of the digital asset space with unwavering commitment to timely, relevant information.
Cardano price surged by 10% amid renewed interest from retail investors, signaling a potential shift in market sentiment. ADA is currently holding strong above the crucial $0.50 support level, showing resilience despite recent market volatility.
This price action comes as the broader crypto market rebounded slightly, gaining 0.73% after experiencing a significant weekly pullback. Buyers have begun stepping in, defending the key support zone and hinting at renewed bullish momentum. The price now consolidates within a narrowing range, pointing to an imminent breakout opportunity.
Cardano Price Eyes $1 Target as Accumulation Trend Gains Momentum
Cardano price may be preparing for a rebound after significant market movements this week. Reports indicate that large holders, known as whales, have offloaded around 4 million ADA. However, this selling pressure appears to be easing, while smaller investors are beginning to accumulate tokens again. Analysts predict Cardano price recovery, which this shift could signal the start of a bullish phase.
Market indicators also show growing confidence. Open interest and derivatives activity are trending bullish, hinting at renewed optimism among traders. With retail investors re-entering and buying pressure strengthening, some market watchers are eyeing a potential move toward the $1 mark. Whether ADA can sustain this momentum remains to be seen, but sentiment across the market is clearly improving.
$ADA Update: Whales sold 4M ADA, but retail accumulation & rising taker buy dominance hint a $1 target
Signs of a shift:
• Whale pressure easing
• Retail re-entering
• Open Interest & derivatives bullish
Could this be the start of ADA’s rebound?
Shared Via @coinexcreators pic.twitter.com/E2lONrgwn5
— Jack (@WispOfDeFi) November 8, 2025
Is ADA Price Preparing for a Major Breakout Above $0.60?
The latest ADA price surged to $0.5626, with more than 10% in the past session. The 4-hour chart reveals that ADA is stabilizing between the $0.50 support and the $0.60 resistance range.
If ADA sustains above $0.55, the next resistance levels are seen around $0.70, $0.80, and $1.00. As the crypto market recovers, the full Cardano forecast report is bullish.
Source: ADA/USD 4-hour chart: Tradingview
However, failure to hold this level could push prices back toward the $0.50 and $0.45 support zones. The MACD indicator currently shows a mild bullish crossover, with the MACD line slightly above the signal line. This suggests improving momentum, though strength remains limited. A continued rise in the histogram bars could confirm an ongoing short-term uptrend. The Relative Strength Index (RSI) stands at 52, hovering near the neutral zone.
2025-11-08 21:271mo ago
2025-11-08 14:001mo ago
Bitcoin – How renewed demand could catch BTC bears off guard
Key Takeaways
What do recent on-chain indicators suggest about Bitcoin’s near-term outlook?
Indicators like a rising Bid-to-Ask Ratio and low Bubble Index suggest Bitcoin may be poised for a bullish move.
How is Bitcoin’s market dominance influencing investor sentiment?
With dominance rising to 59.1%, Bitcoin is attracting more liquidity, reinforcing its role as the market’s anchor.
Bitcoin [BTC] could witness renewed demand in the coming weeks as key on-chain indicators suggest a potential market shift.
The asset has consolidated over the past three days, trading between $101,000 and $103,000.
At press time, the asset exchanged hands at $102,289. This consolidation reflects a temporary balance between buyers and sellers, keeping price volatility contained.
Long-term holders put pressure on Bitcoin
Typically, market dynamics rely on the balance between buyers and sellers. However, this equilibrium has recently shifted.
Long-term holders (LTHs), who control a significant portion of Bitcoin’s supply, have started selling their assets amid weakening demand.
Between November and December 2024, and again from January to March 2025, these holders sold portions of their holdings, but strong demand at the time offset the impact.
Source: CryptoQuant
That trend has now changed. Charts show a decline in apparent demand over the past thirty days as LTHs continue to sell, creating downward pressure on prices.
Meanwhile, the liquidation heatmap shows Bitcoin trapped between two key liquidity clusters. Price movement toward either cluster could define the asset’s next major trend.
Liquidity zones often attract price action, and the current levels stand at $105,000 on the bullish side and $98,000 on the bearish side.
A decisive move beyond either boundary could signal where Bitcoin’s next leg will head.
Where is Bitcoin likely to tilt?
Market fundamentals suggest that bulls could soon make a move. The Bid-to-Ask Ratio, which measures buy-side versus sell-side liquidity, has turned positive for the first time in months, and was sitting at 0.2, at press time.
This reading indicates that buyer liquidity is building as investors begin accumulating Bitcoin.
Source: CryptoQuant
Historically, a similar shift between March and April preceded a major upside move in Bitcoin’s price.
Additionally, the Bitcoin Bubble Index, which gauges whether Bitcoin is in a bullish or bearish phase and identifies potential market tops or bottoms, supports this view.
Typically, a reading near 139 signals a market top. At present, the index stands at 13.46, indicating that the market remains far from its peak and that Bitcoin still has room to rally.
Dominance builds gradually
Bitcoin’s market dominance has remained relatively stable over the past thirty days, reflecting a balance between liquidity inflows and outflows.
In the past 24 hours alone, Bitcoin dominance has risen 0.71%, at press time, bringing its share of total crypto market capitalization to 59.1%.
Source: CoinMarketCap
The total crypto market cap currently sits at $3.45 trillion. A continued rise in dominance suggests that more liquidity is flowing into Bitcoin, reinforcing its position as the market’s focal point.
For now, while long-term holders continue to sell, there’s a strong possibility that fresh demand will begin to build, potentially setting the stage for Bitcoin’s next bullish phase.
2025-11-08 21:271mo ago
2025-11-08 14:001mo ago
Ethereum's Potential Surge to $10,000: Challenges and Opportunities Ahead
Ethereum's price rebounded to nearly $3,500 on a recent Friday, marking a 4.5% increase after initially dipping to $3,200. Despite these fluctuations and an overall decline throughout the month, analysts continue to express optimism about the cryptocurrency's potential for growth.
2025-11-08 21:271mo ago
2025-11-08 14:001mo ago
Is The Bitcoin Price Bottom In? Latest On-Chain Data Suggests So
As the Bitcoin market continues to experience a flurry of sales, which started in mid-October, recent on-chain data paints a somewhat optimistic picture of the cryptocurrency’s future. The question is — is the Bitcoin bottom in?
Is A BTC Price Reversal Imminent?
In a recent Quicktake post on the CryptoQuant platform, pseudonymous crypto pundit Sunny Mom shared that a bottom formation for the Bitcoin price may be around the corner. Sunny Mom’s post was based on four different on-chain metrics, all looking into the behavior of Bitcoin’s market participants.
The first of these is the Futures Taker CVD (Cumulative Volume Delta, 90-day) metric, which helps track the net difference between aggressive buy and sell volumes (referred to as taker orders) in the Bitcoin futures market over the last 90 days.
According to the online pundit, the more dominant sell zones (in red) are turning into neutral zones. This means the leveraged short positions (typically held by the most fearful and aggressive of Bitcoin’s market participants) are slowly taking their exits, thus pointing to the weakening of these speculative hands.
Next, the on-chain analyst referenced data from the Spot Taker CVD (Cumulative Volume Delta, 90-day) metric. Although the number of speculative sellers is declining, the spot CVD still appears to be in the red. Typically, a ‘red’ reading from this metric suggests that Bitcoin’s holders are still selling their coins.
Another interesting event is that the Bitcoin: Stablecoin Supply Ratio (SSR) has fallen to a hallmark low. For context, this metric measures the ratio between Bitcoin’s supply and the supply of stablecoins (like USDT and USDC).
Source: CryptoQuant
A high SSR indicates that there are fewer stablecoins in comparison to Bitcoin. As an extension, it points out that there is lower buying power to purchase Bitcoin in order to send its price to the upside. On the other hand, a low SSR indicates a relative abundance of stablecoins compared to the premier cryptocurrency, suggesting the presence of more potential buying power in the Bitcoin market.
Upon examination of past price action, it is apparent that periods where the SSR read ‘significantly low’ have often preceded significant price rebounds of the flagship cryptocurrency. If history is anything to go by, the analyst inferred that we might be set for another rebound, seeing as the SSR metric currently hovers around a historical low.
Lastly, Sunny Mom explained that data from the Adjusted Spent Output Profit Ratio (aSOPR) also supports the overall conjecture of an imminent price bottom. At the moment, the aSOPR reads around 1.0 — a level whose breach in April 2025 preceded a major price reversal.
Bitcoin Price At A Glance
As of this writing, the price of BTC stands around $102,510, reflecting an over 1% increase in the past 24 hours.
The price of BTC on the daily timeframe | Source: BTCUSDT chart on TradingView
Featured image from iStock, chart from TradingView
2025-11-08 21:271mo ago
2025-11-08 14:141mo ago
New SEC Filing Shows Trump Media's Total Bitcoin Holdings
Trump Media and Technology Group (TMTG) now holds more than 11,500 Bitcoin worth over $1.3 billion, yet the company continues to post steep losses.Meanwhile, several Trump-linked ventures have simultaneously expanded their crypto exposure, bringing their combined holdings into the multibillion-dollar range.The trend reflects a coordinated political and commercial push to frame digital assets as both a strategic reserve and a core part of the administration’s policy agenda.Trump Media and Technology Group (TMTG), the media company associated with US President Donald Trump, now holds more than 11,500 Bitcoin, valued at over $1.3 billion.
The disclosure marks the company’s largest confirmed allocation to date and places it among the biggest public-sector corporate holders of Bitcoin.
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TMTG Bitcoin Holdings Fail to Yield GainsTMTG accelerated its pivot earlier this year when it formally adopted Bitcoin as a core reserve asset.
At the time, TMTG said the company turned to BTC to protect itself from what he described as harassment and discriminatory treatment by financial institutions.
That argument tied Trump Media’s strategy to a wider corporate trend in which firms use Bitcoin to limit perceived dependence on banks that can freeze, slow, or scrutinize accounts.
Trump Media’s Bitcoin Holdings. Source: SECMeanwhile, the company’s holdings extend beyond Bitcoin. TMTG reported owning roughly 756 million Cronos (CRO) tokens, worth approximately $110 million.
The position reflects the company’s growing alignment with Crypto.com, a relationship that has already produced several crypto-focused initiatives, including exchange-traded products and promotional tie-ins.
These initiatives helped position TMTG as a more active participant in the crypto economy, even though they have not reversed the firm’s financial challenges.
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TMTG posted a $54.8 million net loss in the third quarter of 2025, extending its stretch of multi-million-dollar quarterly losses.
This suggests that the company’s crypto-heavy strategy has therefore served more as a political and operational statement than a source of near-term financial relief.
Trump’s Family Crypto Holdings SurgeAs TMTG increased its exposure, other Trump-connected ventures expanded theirs as well, creating a broader cluster of politically adjacent crypto holdings.
Data from Arkham Intelligence indicates that several affiliated entities now hold substantial balances.
Other notable Trump Family entities:
Donald Trump: holds $861K in crypto
World Liberty Fi: holds $5.76B in crypto
Official Trump Meme: holds $6.30B in crypto
Official Melania Meme: holds $19.65M in crypto
Trump Cards: holds $29.72K in crypto pic.twitter.com/T12F6yP4Oh
— Arkham (@arkham) November 8, 2025
Trump personally holds about $861,000 worth of digital assets, while World Liberty Financial, one of the largest Trump-associated projects, controls more than $5.7 billion in crypto.
Additional holdings include $6.3 billion tied to Official Trump Meme, $19.65 million linked to Official Melania Meme, and nearly $30,000 associated with the Trump Cards collection.
These positions grew as the White House intensified its pro-crypto messaging, which shaped both the political environment and the commercial incentives for Trump-aligned ventures to deepen their involvement.
Taken together, the holdings show a coordinated embrace of digital assets across Trump-linked entities. They also reflect the administration’s broader effort to position crypto as both a strategic asset and a policy priority.
Disclaimer
In adherence to the Trust Project guidelines, BeInCrypto is committed to unbiased, transparent reporting. This news article aims to provide accurate, timely information. However, readers are advised to verify facts independently and consult with a professional before making any decisions based on this content. Please note that our Terms and Conditions, Privacy Policy, and Disclaimers have been updated.
2025-11-08 21:271mo ago
2025-11-08 14:161mo ago
Bitcoin Bottom May Be Forming as Analyst Predicts Final Bullish Leg Before Year-End
Bitcoin's recent selloff has shaken investor confidence, but veteran trader Trader Mayne believes the current dip could mark a critical cycle low before another major move higher. Despite widespread liquidations and sharp volatility, Mayne insists the bull cycle isn't over yet—and the market may be setting up for a final surge heading into the end of 2025.