Proti společnosti D-Wave Quantum (QBTS) byla podána hromadná žaloba investorů kvůli údajnému nadhodnocování obchodních a finančních vyhlídek; lhůta pro podání žádosti o jmenování hlavním žalobcem je 15. prosince 2026.
Faruqi & Faruqi, LLP Securities Litigation Partner James (Josh) Wilson Encourages Investors Who Suffered Losses In D-Wave Quantum To Contact Him Directly To Discuss Their Options
If you purchased or acquired securities in D-Wave Quantum between February 26, 2026 and August 25, 2026 and would like to discuss your legal rights, call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983-9330 (Ext. 1310).
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New York, New York--(Newsfile Corp. - October 25, 2026) - Faruqi & Faruqi, LLP, a leading national securities law firm, is investigating potential claims against D-Wave Quantum Inc. ("D-Wave Quantum" or the "Company") (NASDAQ: QBTS) and reminds investors of the December 15, 2026 deadline to seek the role of lead plaintiff in a federal securities class action that has been filed against the Company.
Faruqi & Faruqi is a leading national securities law firm with offices in New York, Pennsylvania, California and Georgia. The firm has recovered hundreds of millions of dollars for investors since its founding in 1995. See www.faruqilaw.com.
As detailed below, the complaint alleges that the Company and its executives violated federal securities laws by making false and/or misleading statements and/or failing to disclose that: Specifically, Defendants made false and/or misleading statements and/or failed to disclose that: (i) Defendants materially overstated D-Wave's business and financial prospects; (ii) the foregoing was reasonably likely to negatively impact the Company's business and reputation; and (iii) as a result, Defendants' public statements were materially false and misleading at all relevant times.
On August 6, 2026, D-Wave announced its financial results for the second quarter of 2026, reporting revenue of just $3.08 million, compared to $3.1 million for the same period in the prior year, falling short of analyst expectations ranging from $4.03 million to $4.08 million. On this news, D-Wave's stock price declined $1.99 per share, or 9.28%, to close at $19.41 per share on August 6, 2026.
On August 25, 2026, D-Wave issued a press release "announc[ing] that John Markovich is retiring and thus resigning from his position as Chief Financial Officer effective September 2, 2026." On this news, D-Wave's stock price fell $1.84 per share, or 9.51%, closing at $17.51 per share on August 26, 2026.
The court-appointed lead plaintiff is the investor with the largest financial interest in the relief sought by the class who is adequate and typical of class members who directs and oversees the litigation on behalf of the putative class. Any member of the putative class may move the Court to serve as lead plaintiff through counsel of their choice, or may choose to do nothing and remain an absent class member. Your ability to share in any recovery is not affected by the decision to serve as a lead plaintiff or not.
Faruqi & Faruqi, LLP also encourages anyone with information regarding D-Wave Quantum's conduct to contact the firm, including whistleblowers, former employees, shareholders and others.
To learn more about the D-Wave Quantum class action, go to www.faruqilaw.com/QBTS or call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983-9330 (Ext. 1310).
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Frequently Asked Questions (FAQ) for Investors Regarding the D-Wave Quantum Securities Class Action Lawsuit:
What is the D-Wave Quantum securities fraud lawsuit about?
The lawsuit alleges that D-Wave Quantum Inc. and certain of its officers and directors made materially false and misleading statements and/or failed to disclose material information during the Class Period. Specifically, the complaint alleges that Defendants materially overstated D-Wave's business and financial prospects, and that this alleged misrepresentation was reasonably likely to negatively impact the Company's business and reputation. As a result, the lawsuit alleges that Defendants' public statements were materially false and misleading at all relevant times during the Class Period. The action was filed on behalf of investors who suffered damages as a result of their reliance on those allegedly false and misleading statements.
Who may be eligible to participate in the lawsuit?
Investors who purchased or otherwise acquired D-Wave Quantum Inc. (NASDAQ: QBTS) securities between February 26, 2026 and August 25, 2026, inclusive, may be eligible to participate in this lawsuit. Eligibility is not limited to those who seek appointment as lead plaintiff; any class member who suffered losses during the Class Period may potentially share in any recovery obtained. Investors are encouraged to review their trading records for the relevant period to assess whether they purchased QBTS securities during the Class Period. Faruqi & Faruqi, LLP invites potentially affected investors to contact the firm to discuss their legal rights and options.
What is a lead plaintiff, and how can I seek appointment?
A lead plaintiff is a court-appointed representative who acts on behalf of all class members and plays an active role in directing the litigation, including working with counsel to make key strategic decisions in the case. Any investor who purchased D-Wave Quantum securities during the Class Period and suffered a loss may move the court for appointment as lead plaintiff by the applicable lead plaintiff deadline. Courts typically appoint the movant with the largest financial interest in the relief sought, provided that movant satisfies the relevant legal requirements. Importantly, investors need not serve as lead plaintiff to share in any recovery that may be obtained; class members who do not seek appointment may still participate in any settlement or judgment.
Why should investors contact Faruqi & Faruqi, LLP?
Faruqi & Faruqi, LLP has represented investors in securities litigation for decades and has recovered hundreds of millions of dollars for shareholders. Investors who purchased D-Wave Quantum securities during the Class Period may contact the firm to discuss their legal rights, potential claims, and the lead plaintiff process at no cost or obligation.
Attorney Advertising. The law firm responsible for this advertisement is Faruqi & Faruqi, LLP (www.faruqilaw.com). Prior results do not guarantee or predict a similar outcome with respect to any future matter. We welcome the opportunity to discuss your particular case. All communications will be treated in a confidential manner.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/320642
Source: Faruqi & Faruqi LLP
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When a miner finally stops digging holes in the balance sheet and starts pulling consistent profit from the ground, the math usually catches up to the reality. Eldorado Gold (EGO -3.77%) is currently in that rare transition window. Operating a diverse portfolio of gold, silver, lead, and zinc mines across Turkey, Canada, Greece, and Romania, it has spent the better part of a half-decade wrestling with heavy capital requirements and complex jurisdictional hurdles. As of October 23, 2026, the stock trades at $31.67 and has posted a 1-year return of 26%, reflecting a market that is finally pricing in the output from its major infrastructure projects.
Our proprietary Hidden Gems scoring system assigns Eldorado Gold an overall Superscore of 80 out of 100, placing it in the Strong category. The Superscore is an AI-powered score that evaluates a company's overall strength by combining financial performance, product market position, technological capabilities, leadership quality, and relative valuation. It represents the unification of all our scores into a single score for public companies, with five rating bands: Exceptional (90-100), Strong (75-89), Above Average (60-74), Average (40-59), and Cautious (0-39). This 81 places the company in the Top ~9% of every company we score. This score-driven analysis is meant to serve as a research starting point; investors should weigh these operational strengths against the inherent risks outlined below before making an investment decision.
Why EGO Has an 80 SuperscoreRevenue breakout momentum: Revenue jumped 40% year over year in fiscal 2025, signaling that the company has moved past years of stagnation and effectively scaled production at its core assets.Operational margin expansion: Operating margins surged to 41% in fiscal 2025, proving that the company can turn its increased mining output into legitimate bottom-line results.Strategic commodity diversification: The acquisition of Foran Mining and the integration of the McIlvenna Bay operation provide a significant copper-zinc mix, reducing the company's historical reliance on gold price volatility alone.Why Is EGO's Superscore Not Higher?Capital expenditure burden: Aggressive spending on infrastructure projects like Skouries resulted in negative free cash flow of $195 million in fiscal 2025, which limits the company's short-term financial flexibility.Project execution risks: Unexpected $155 million capital overruns at Skouries demonstrate that management can struggle with labor productivity and cost forecasting when building in complex environments.Elevated price-to-sales multiple: The stock trades at a trailing price-to-sales ratio of 2.94, a level that leaves little margin for error if commodity prices cool or production targets slip.Commodity price sensitivity: The business remains a price-taker in liquid global markets, meaning its profitability is inherently tied to gold and copper cycles that the company cannot control.Eldorado Gold is a highly capital-efficient business, earning a top-tier rank for returns on net tangible assets. Because it produces outsized profits on a relatively small base of physical assets, the market tends to pay a premium for that efficiency, assuming the company can sustain its current operational leverage.
Table 1: Hidden Gems Database Scores for Eldorado Gold (EGO)ScoreScore (out of 100)RankSupporting Data PointProduct (1Y)85Top ~11%Exceptional momentum driven by the successful operational scaling of the Skouries project.Product (5Y)68Top ~34%Consistent 12.5% revenue CAGR reflects a stable transition from mid-tier volatility to a reliable producer.Financial (1Y)80Top ~13%Fiscal 2025 marked an inflection point where heavy development capital shifted into realized revenue growth.Financial (5Y)74Top ~16%Revenue expanded from $871 million in 2022 to $1.85 billion in 2025, showing sustained recovery.Leaders72Top ~39%Management demonstrates transparency in disclosing project overruns, though execution planning remains a variable.AI29Top ~35%The company's core extraction model is not positioned to capture value from the AI transition.Valuation Risk85Top ~2%The stock trades at a trailing P/E of 10.07, suggesting an attractive valuation relative to recent cash flows.Is EGO Right For Your Portfolio?This stock warrants a closer look if...
You want exposure to gold and copper producers that function as alternatives to typical gold ETFs.You are hunting for a mining operation that has successfully transitioned from negative cash flow to a scalable profit generator.You may want to keep researching before buying if...
You are uncomfortable with the risks associated with the high capital intensity and project ramp-up timelines inherent in the mining sector.You believe the stock's current valuation multiple is already fully pricing in the anticipated production gains from new copper-gold assets.This Superscore is one data-driven signal worth investigating, not a stand-alone buy recommendation; weigh it against your own research, financial goals, and risk tolerance.
My 5-year prediction for EGO stockAs with many mining names, Eldorado's defining risk for the past half-decade has been execution, but 2026 is the year that risk started converting into output. Skouries in Greece, the $2 billion-plus copper-gold project that absorbed years of capital and a $155 million overrun, produced its first concentrate on September 8 and is targeting commercial production this quarter. A stockpile of more than 4.6 million tonnes of above-reserve-grade ore covers over seven months of plant feed, and in mid-October the European Commission granted the mine strategic-project status, easing future permitting and financing.
Meanwhile, the firm's C$3.8 billion Foran Mining acquisition closed in April, and the McIlvenna Bay copper-zinc mine in Saskatchewan poured first copper concentrate in June, with commercial production also expected imminently. Together, the two assets are designed to transform Eldorado into a diversified gold and copper producer, and management is guiding for roughly 40% gold production growth in 2027 versus 2025 once Skouries reaches steady state.
Eldorado's history shows how budgets and timelines slip, and the valuation assumes its mines deliver. But with both projects past their riskiest construction phases and third-quarter results due within days, the setup favors patient shareholders, and Eldorado seems poised for outperformance over the next five years as two decades-long assets hit their stride at once.
The Hidden Gems Superscore reflects The Motley Fool's proprietary AI-driven evaluation of a company across product, financial, leadership, and valuation pillars as of the article date and may change over time. Performance figures are point-in-time. Past performance does not guarantee future results.
Tilray po akvizici BrewDog zvýšil tržby z alkoholu na 101,5 mil. USD, čímž překonal 56,1 mil. USD z konopí, a v 1. čtvrtletí fiskálního roku 2027 dosáhl rekordních tržeb.
Tilray (TLRY -4.10%) isn't just a pot company anymore. In fact, you might argue that it is more of a beer company than a marijuana company at this point. And that could be exceptionally good news for investors, since the company is now more diversified. Here's why Tilray has chosen to go down this path, the key milestone it just achieved, and why it points to a brighter long-term future.
Wall Street loves a good story When Tilray went public, marijuana was all the rage. Pot was increasingly being legalized, and investors believed it would be a huge growth opportunity. Tilray's stock rocketed higher. But it wasn't the only company trying to capitalize on the dynamics in the marijuana sector. A large number of companies jumped in, creating intense competition.
Image source: Getty Images.
And then there was the old competition, illegal sellers, that didn't go away. It turned out to be harder than expected to turn a profit in the marijuana sector. When investors realized that fact, they dumped pot stocks, including Tilray. Today, Tilray's stock price is roughly 99% below its all-time high set shortly after its initial public offering. That said, it has managed to survive and adapt.
Tilray goes down a different road At this point, it is clear that marijuana demand will grow over time. So it isn't a bad business to be in. However, it is also clear that the opportunity isn't as exciting as it seemed at first. This is why Tilray began investing in alcoholic beverages, positioning itself as "a global lifestyle and consumer packaged goods company." Its focus is now spread across beverages, marijuana, and wellness. (Wellness basically means CBD-related products.)
In fiscal 2026, the company made an important acquisition, buying beverage company BrewDog. That has transformed the portfolio, with alcoholic beverages generating $101.5 million in revenue in the first quarter of fiscal 2027, up from $55.7 million in the same quarter of 2026. Marijuana revenues came in at $56.1 million, down from $64.5 million in the first quarter of fiscal 2026. Tilray is an entirely different business today than it was a year ago.
While there is still opportunity for growth in the marijuana sector, the core of the company's business is its beverage operations. That's a far more developed industry and one that is likely to be fairly predictable. In other words, Tilray has created a stronger foundation from which to grow. As an investor, you should probably see that as a very positive shift.
TLRY Tilray Brands$2.81-$0.12 (-4.10%)
NASDAQ · As of 4:00 PM ET 10/23/26
Tilray still has a lot of work to do The growth of the beverage business wasn't the only positive from the fiscal first quarter of 2027. Tilray also reported record revenues and improved its gross margin by three percentage points. Moreover, it reduced debt in the quarter, ending the period with a net cash position (meaning it had more cash than debt on its balance sheet).
There's just one not-so-small problem: Tilray is still bleeding red ink. So while progress is being made from a business perspective, from a profit perspective, the company remains a big investment risk. Clearly, Tilray's long-term goal is to be a sustainable and profitable business. The beverage shift is part of the process of achieving that goal, but only more aggressive growth investors are likely to find the stock interesting at this point.
But even more conservative investors may want to keep Tilray on the watch list. If it does manage to become sustainably profitable, it could be an interesting way to add marijuana exposure to your portfolio without jumping into the still-developing pot sector with both feet.
Home Depot nevyužije rozšiřování elektronických cenovek k dynamickému ani personalizovanému stanovování cen; zákazníci by měli za stejný produkt ve stejný den platit stejnou cenu.
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The Home Depot's chief information officer told Business Insider that electronic price labels can help delivery workers work more efficiently. Brandon Bell/Getty Images Buying a screwdriver at Home Depot?
Well, you and your next-door neighbor should be paying the same price for the same product on the same day.
Angie Brown, the home improvement retailer's executive vice president and chief information officer, told Business Insider that it's exploring a larger rollout of its electronic shelf labels, or ESLs — the small digital placards that large retailers have been using to replace paper price tags.
When asked if those wireless-updatable tags could introduce dynamic pricing, Brown responded, "Absolutely not."
Instead, The Home Depot uses those tags to accurately inform customers when their store expects the next delivery of a specific product, Brown said.
Home Depot IT chief says its digital price tags won't give consumers different prices
"We love being able to show you on the sign, 'You can get this as soon as the next day,'" she said. "And we want that to be right."
Why those little shelf electronic labels have caused so much worry
An electronic shelf label in a Best Buy. : Lindsey Nicholson/UCG/Universal Images Group via Getty Images Several major brands — including Walmart, Kroger, Best Buy, and Whole Foods — have rolled out electronic shelf labels in their stores.
Consumers have scrutinized the rollout amid fears that stores could quickly raise prices during busy shopping periods or use customer data to show different prices to separate shoppers.
Some state lawmakers have responded to that anxiety, too. New Jersey passed a yearlong moratorium on new implementation of the tech. Maryland passed legislation requiring grocery stores to keep electronically displayed prices unchanged for a full business day.
Concerns have prompted retailers to get ahead of dynamic pricing concerns: Walmart's CEO, John Furner, for example, wrote a memo in September to customers and employees, explicitly stating that the technology wouldn't be used to adjust prices.
"We don't set different prices based on who you are or the time of day, and we won't," he wrote. "We price the product, not the person."
Target also shared a similar statement this month, saying that the company "does not use personal information to raise prices."
Electronic signs in Home Depot
The Home Depot has been using ESLs for several years. They're common in the appliance section, Brown said. Mario Tama/Getty Images Home Depot has been testing the technology for years. In its 2020 annual report, the retailer said it had initially used electronic shelf-label capabilities in the appliances section before trying them in additional merchandising departments.
Brown said Home Depot sees the labels as a tool for store operations, not a new pricing strategy.
As stores increasingly double as fulfillment hubs for delivery workers and pickup orders, she said, ESLs can light up to help gig workers and employees quickly locate a product — an update that Walmart rolled out in its stores earlier this month.
She also said the company is not using the technology in its garden department.
There are two important caveats.
First, Home Depot sells several commodities, such as building materials and garden goods. Brown said the ESLs will reflect the individual commodity markets.
Second, Home Depot's Pro customers can receive bulk discounts when they cross purchasing thresholds. Brown said those prices are set by transparent rules, not by a shopper's personal data.
Still, for everyone else walking through a Home Depot aisle, she said, the promise is simpler: The price one customer sees should be the same price another customer sees.
"Those are the use cases we're interested in, not in changing price more often because we have electronic shelf labels," she said. "We've never talked about changing our pricing strategy if we were to roll out ESLs."
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Ben Shimkus You're currently following this author! Click to unsubscribe from email alerts.
Ben Shimkus is a reporter for the Business News desk. He writes about cars, transportation, retail, and jobs. Ben's reporting has appeared in Rolling Stone, The Verge, Automotive News, USA Today, AutoBody News, LGBTQ Nation, TopSpeed, and Out Magazine. He's also held staff writing positions at The U.S. Sun and the Daily Mail. He graduated from NYU with a Master's in journalism in 2024. Email Ben at [email protected] or message him privately on Signal at bshimkus.41.
Společnost Broadcom zvýšila v první polovině roku 2026 tržby o 55 % na 71 mld. USD a čistý zisk o 103 % na téměř 30 mld. USD díky poptávce po čipech pro AI.
Attempting to predict the performance of Broadcom (AVGO -0.48%) may not be as easy as some assume. Indeed, the unprecedented demand for AI chips led to an approximate 560% gain for its stock over the last five years.
Nonetheless, history shows that uninterrupted increases are rare, and investors may worry about the pace of AI growth. Thus, investors should expect more muted and uneven growth for Broadcom over the next five years. Here's why.
Image source: The Motley Fool.
Optimism and worry about Broadcom's future
From a certain point of view, investors may naturally expect Broadcom's growth to continue. Although market research firms may disagree on the scale of industry expansion, they have forecast industry growth rates between 16% and 33% annually in the coming years.
Broadcom's semiconductor solutions segment far exceeded those predictions, growing 88% year over year in the first half of 2026. Even when including the infrastructure software segment, Broadcom's total revenue of $71 billion increased by 55% over the same period.
Moreover, since the company kept operating expenses in check, net income for the same period was almost $30 billion. That was a 103% rise from year-ago levels and has helped lower the stock's valuation. Broadcom's P/E ratio of 43 may make it appear pricey, but the forward P/E ratio of 29 suggests that the stock price growth has not moved meaningfully ahead of its fundamentals.
AVGO Broadcom$321.68-$1.56 (-0.48%)
NASDAQ · As of 4:00 PM ET 10/23/26
However, investors should remember that, just as the internet industry endured the dot-com bust, the same could happen to AI. Unfortunately, investors cannot dismiss the possibility of such an event over the next five years. Interestingly, Broadcom CEO Hock Tan echoes Warren Buffett on some of the "casino-like investing" that has often characterized AI stock investing.
Such attitudes do not appear to apply as directly to Broadcom. Unlike many AI enterprises, it is a profitable company and, as previously mentioned, also has a software division that can mitigate chip industry downturns.
Nonetheless, such a down cycle has followed every previous growth phase in the industry. Furthermore, rising interest rates, as the market has experienced recently, typically contribute to such downturns.
For now, analysts forecast 66% revenue growth for Broadcom this year and 64% in 2027. But since forecasts can change, it is probably wise for investors to be prepared for more challenging conditions.
Moving forward with Broadcom stock
Over the next five years, investors should probably maintain a bullish outlook on Broadcom, but they should not simply expect five years of uninterrupted growth.
Admittedly, Broadcom's chip division is experiencing massive growth, and forecasts for both Broadcom and the AI chip industry generally point to continued optimism.
Although that growth is likely to continue, the history of such booms should urge caution. Just as rising interest rates contributed to the dot-com bust, it is possible that the AI industry could experience a similar sell-off over the next five years.
Such an event probably does not mean AI is dead, but it is a reminder that significant sell-offs usually accompany industry growth stories.
The good news is that Broadcom is an established and profitable company at the center of this industry. That means the chip stock should roll with the punches and remain one of the largest beneficiaries of AI expansion.
Spotify Technology (SPOT +0.10%) not only saw its third-quarter headline net income fall, but it also whiffed on the consensus analyst estimate. Given that, you'd imagine that investors would have reacted by aggressively selling the music streamer's stock. Well, you'd be very wrong.
The opposite occurred on Thursday after the company published its earnings release -- market players couldn't wait to buy its stock, and it handily beat the S&P 500 index, rising nearly 4%. On Friday, it ticked higher. Let's look at the company's numbers and tease out why it scored such a big win from an ostensibly losing quarter.
Image source: The Motley Fool.
Music to their earsSpotify's quarter was headed by a revenue line that hit almost 5 billion euros ($5.6 billion), for robust year-over-year growth of 16%. By far the bulk of the company's top line comes from its premium services; the take from these rose by 17% to nearly 4.5 billion euros ($5 billion). The remainder came from ad-supported offerings, which collectively rose 10% to 482 million euros ($540 million).
Spotify also managed to grow both its total user base and the crucial segment of that population, premium-service subscribers. The company's total monthly active user (MAU) count rose 11% to 788 million, while the premium subscriber tally increased 9% to 306 million.
Attributable net income, however, went in the opposite direction. It fell to 518 million euros ($580 million) from the year-ago profit of 899 million euros ($1 billion). On a per-share basis, the former result was 2.48 euros ($2.78).
While that revenue number was essentially in line with the consensus analyst estimate, Spotify fell short on profitability. Analysts tracking the stock were modeling net income of 2.84 euros ($3.18) for the quarter.
That bottom-line swoon looked ugly on paper, but it wasn't as grim as it appeared. In the third quarter of 2025, the company benefited enormously from significant finance income derived from share, bond, and warrant valuations, which affected the accounting. It also recorded a 72 million euro ($81 million) tax benefit during that period.
Spotify watchers are aware that these items distorted the 2025 frame's profitability, so the year-over-year drop wasn't particularly concerning to them. They were also impressed that the company topped its guidance for operating income, which came in at 672 million euros ($753 million), and notched a new record for gross margin at 33%. And for a stock increasingly evaluated on free cash flow (FCF), the 735 million euros ($823 million) in FCF it generated during the quarter was heartening.
$584.22+$0.56 (+0.10%)
NYSE · As of 4:00 PM ET 10/23/26
Streaming forwardSpotify has an enviably high number of growth opportunities. Management ticked off several major ones, including a major expansion of its relatively recent audiobook business, from the current 22 countries to over 180. Meanwhile, artificial intelligence (AI) is at a relatively early stage of deployment for the company; it plans to harness it to offer subscribers more and increasingly varied custom services -- AI playlists, anyone? -- to enhance the listening and music-curating experiences.
It's confident that this will keep those subscriber and fundamental numbers rising. It proffered guidance for its current (fourth) quarter of 818 million MAUs, which, if achieved, would be nearly 9% higher than in the same period of 2025. It's also counting on a sub-9% increase in premium subscribers (to 316 million). As for key financials, management is expecting another pop in revenue, by almost 15% to 5.2 billion euros ($5.8 billion). Operating income is projected to surge 17% to 820 million euros ($919 million). It did not provide a net income forecast.
I feel that, if anything, Mr. Market's reaction to Spotify's third quarter was muted and conservative. The company has established itself as the clear king of streaming music and, increasingly, other aural entertainment options like audiobooks. I feel it's building quite the imposing moat, which more than justifies the valuations that likely moderated investors' reaction to the earnings release (its forward P/E is approaching 52). Yet this company is becoming ever more powerful, and it clearly aims to tap into the numerous, high-potential growth opportunities before it. I'd be a buyer of this stock, even at its seemingly lofty level.
Neurocrine Biosciences (NBIX -0.41%) generated $959 million in revenue in Q2 2026, representing an increase of 39% year over year. Its flagship drug, Ingrezza, continues to deliver double-digit percentage sales growth, while two newer treatments help the company expand beyond its original neurological disease franchise. Neurocrine is also approaching several important clinical milestones, including late-stage trial results for experimental treatments targeting depression and schizophrenia.
By 2031, I expect Neurocrine to be a substantially larger pharmaceutical company, potentially generating more than $6 billion in annual revenue. Whether its stock follows that growth, however, will depend on the success of its newer drugs and how much investors are willing to pay for its earnings.
Ingrezza remains the foundation
If you're unfamiliar, Ingrezza treats tardive dyskinesia, a neurological condition that causes involuntary movements, often associated with long-term use of certain psychiatric medications. It's also approved to treat chorea (involuntary muscle movements) associated with Huntington's disease.
In Q2, Ingrezza sales reached $716 million, up 15% from $624 million a year earlier. Management subsequently raised its full-year 2026 Ingrezza sales forecast to between $2.825 billion and $2.875 billion. And there's still room for more growth.
$142.70-$0.59 (-0.41%)
NASDAQ · As of 4:00 PM ET 10/23/26
Neurocrine estimates that about 800,000 Americans have tardive dyskinesia. Many patients remain undiagnosed or untreated, providing an opportunity to expand prescriptions without requiring another Food and Drug Administration (FDA) approval.
To be sure, Ingrezza does face competition from Teva Pharmaceuticals' (TEVA -1.99%) Austedo, which also treats tardive dyskinesia and Huntington's-related chorea. Future pricing pressure, changes in insurance reimbursement, and eventual generic competition could limit growth. Still, I expect Ingrezza to remain Neurocrine's largest product by 2031, although the company's dependence on it should decline significantly.
Two newer drugs are becoming major revenue contributors
Neurocrine's second-largest product is Crenessity, approved in December 2024 to treat classic congenital adrenal hyperplasia (CAH). This is a rare inherited disorder that interferes with the body's ability to produce certain hormones. Patients often require long-term steroid treatment, which can cause serious complications.
Q2 sales reached $184 million, compared with $53 million a year earlier. That's an increase of 247%. Annualizing the latest quarter produces a revenue run rate of $736 million, although actual full-year sales will depend on continued prescription growth and reimbursement. Neurocrine estimates at least 20,000 Americans have CAH, giving the company a relatively small but commercially meaningful patient population.
Image source: Getty Images.
The company acquired Soleno Therapeutics for about $2.9 billion in May, adding Vykat XR to its portfolio. Vykat XR treats hyperphagia, or persistent, excessive hunger, in patients with Prader-Willi syndrome, a rare genetic disorder.
The drug generated $54 million in sales between the May 18 acquisition closing and June 30. Including sales recorded before the acquisition, the drug generated about $94 million during the full second quarter, equivalent to an annualized revenue run rate of $376 million.
Combined, Crenessity and Vykat XR are already generating more than $1 billion in annualized revenue. Continued adoption could make both significant contributors by 2031.
The pipeline could produce additional blockbusters
Neurocrine has several experimental treatments approaching important clinical milestones. There's Osavampator, which is being evaluated in Phase 3 trials for major depressive disorder, while direclidine is undergoing Phase 3 testing for schizophrenia. Both programs are expected to produce trial results in 2027.
These are considerably larger markets than those targeted by Crenessity and Vykat XR. However, psychiatric drug development carries substantial clinical risk. Both treatments must show meaningful benefits and an acceptable safety profile before Neurocrine can even seek regulatory approval. The company is also developing additional neurological treatments, including experimental drugs targeting Alzheimer's disease and epilepsy.
What could Neurocrine look like in 2031?
Neurocrine's Q2 revenue of $959 million represents an annualized run rate of about $3.84 billion. If annual revenue grows at a compounded rate of 10% from that baseline during the next five years, it would reach about $6.18 billion. A 12% growth rate would produce roughly $6.76 billion.
Those are achievable scenarios if Ingrezza continues growing, Crenessity and Vykat XR expand their patient populations, and at least one late-stage pipeline candidate reaches commercialization.
Neurocrine reported Q2 net income of about $144 million, showing it already has a profitable commercial business to support further research and acquisitions. The biggest risks are really clinical trial failures, rising development expenses, and pricing pressure on Ingrezza.
I expect Neurocrine to generate $6 billion to $7 billion in annual revenue by 2031, with a broader portfolio and less dependence on any single drug. That would represent substantial growth from today's business. But be sure to pay particular attention to the company's 2027 clinical readouts, which could determine whether Neurocrine becomes a much larger neuroscience franchise or remains primarily a three-product pharmaceutical company.
Berkshire Hathaway v první polovině roku 2026 odkoupila své akcie za zhruba 4,8 mld. USD, zatímco provozní zisk ve 2. čtvrtletí meziročně vzrostl o 16 % na 13 mld. USD.
Berkshire Hathaway (BRKA -0.84%)(BRKB -0.87%) stock is finally back at a record. On Oct. 20, the Class B shares ended at $539.82, inching past a record close from May 2, 2025 -- the day before Warren Buffett told shareholders he planned to hand the CEO job to Greg Abel.
As I write, the shares trade near $548, up about 9% this year.
The new high comes in a year when Berkshire has gone back to buying its own stock. It repurchased nothing in 2025. In the first half of 2026, its buybacks came to around $4.8 billion. And it only buys if its CEO thinks the shares cost less than the business is worth.
But Berkshire paid around $476 to $488 a Class B share in May and June. With the stock at least 12% higher today, is it still a buy?
Image source: Getty Images.
Berkshire bought more as the year went byThe buying started small. In March, Berkshire repurchased around $234 million of stock at an average of about $487 a Class B share, according to its first-quarter 10-Q.
Then it sped up. After a quiet April, Berkshire spent around $740 million on shares in May at an average Class B price of about $476, and about $3.8 billion in June at about $488, for a second-quarter total of about $4.5 billion. And the cover of the second-quarter 10-Q suggests the buying kept going. Berkshire had around 4,550 fewer Class A-equivalent shares outstanding on July 29 than on June 30 (one Class A share equals 1,500 Class B shares).
At the $488 to $512 range where the Class B shares closed in July, these repurchased shares total about $3.4 billion of stock in under a month.
"We will buy back Berkshire shares when they trade below our estimate of intrinsic value, conservatively determined," Abel said in his first annual letter to shareholders in February.
Intrinsic value is Berkshire's term for what the whole business is worth, whatever the stock does day to day. Put another way, every month of buying was Abel saying the shares were cheap at around $476 to $488.
I'd argue these purchases tell Berkshire shareholders more about the stock's value than anything else from the company's filings this year.
A higher price tagAt around $548, the Class B shares cost about 12% more than Berkshire's average price in June and about 15% more than its average in May.
Berkshire reported $747.9 billion in shareholders' equity on June 30, up $30.5 billion from the end of 2025. That's around $348 of book value per Class B share (book value is what's left of a company's assets after subtracting its liabilities). June's average buyback price put Berkshire at about 1.4 times that book value. Today's price is nearly 1.6 times book value.
Of course, book value isn't fixed at its June figure, and more growth in the third quarter might shrink the gap.
Berkshire's third-quarter 10-Q should show how Abel sees that gap, because the filing lists buybacks month by month with the average price paid. The Class B shares closed over $500 on 44 of the 64 trading days from July through September.
If Berkshire kept buying in August and September, that might signal Abel's estimate of value has gone up with the business. If the buying ended, the prices Berkshire paid in May and June could be near the most Abel is willing to pay.
$542.19-$4.78 (-0.87%)
NYSE · As of 4:00 PM ET 10/23/26
Berkshire's earnings are still growingShowing why that estimate might have kept climbing, Berkshire's second-quarter operating earnings (which leave out the swings in its huge stock portfolio) rose 16% year over year, to around $13 billion. That's up from about $11.2 billion a year before and around $11.3 billion in 2026's first quarter. But currency shifts on Berkshire's foreign-currency debt flattered the comparison. They added an after-tax gain of $326 million in this year's second quarter, versus an $877 million loss in the second quarter of 2025. Excluding foreign exchange, operating earnings rose around 5%.
Mid-single-digit growth is still steady progress for a company this big.
Still, should you buy Berkshire stock at a record high?
I think it's worth considering, maybe a little at a time. The businesses keep growing, and Berkshire seems to have been buying its own shares as recently as July. But at almost 1.6 times book value, the stock isn't the bargain Berkshire was buying in June.
The AI boom has created an urgent problem: Data centers need enormous amounts of power, and the electric grid can take years to catch up. That bottleneck has opened the door for power equipment providers like Bloom Energy (BE -11.24%) to become a critical bridge power provider for hyperscalers.
Data center demand has been an incredible tailwind, sending Bloom's stock soaring 2,085% since November 2024. The narrative around Bloom Energy has changed in recent years, as the company transforms from a speculative renewable hydrogen play into a data center power story.
The next five years will determine whether Bloom's incredible growth is durable or simply a temporary surge. Here's what Bloom needs to do to keep winning in the coming years.
$193.30-$24.47 (-11.24%)
NYSE · As of 4:00 PM ET 10/23/26
Bloom Energy secured several major deals in recent years
Over the past several years, Bloom Energy has secured numerous large deals to power utilities and data centers. In November 2024, Bloom signed a landmark deal with American Electric Power for up to 1 gigawatt (GW) of power from its solid-oxide fuel cells (SOFCs). The deal started with a 100 MW order, and earlier this year, American Electric exercised its option for the remainder.
Bloom Energy also has deals with Oracle and Brookfield Asset Management. In April, Bloom expanded on its deal with Oracle to deploy 2.8 GW of fuel cell capacity. Oracle was an early customer that validated Bloom's time-to-power advantage when Bloom delivered its fuel cells well ahead of its 90-day target.
Image source: The Motley Fool.
Meanwhile, Brookfield Asset Management expanded its partnership with Bloom to $25 billion in June, up from their original $5 billion agreement last year.
Bloom Energy will scale manufacturing in the coming years
Next up for Bloom Energy is scaling up manufacturing capacity and delivering on these massive agreements. The company is taking steps to double its near-term run-rate capacity to 2 GW annually, while expanding its industrial footprint. As part of this, Bloom acquired a 158,000-square-foot facility in Fremont, California, to go with its existing 164,000-square-foot plant.
Long-term, Bloom thinks it can scale up to 5 GW in annual capacity. Bloom is scaling its manufacturing using "copy exact" modular increments. One benefit for Bloom is that its return on investment for capacity expansion comes in a few months, not years, as it often does for traditional industrial manufacturers.
With cash on its balance sheet and external financing, Bloom is well capitalized to fund this expansion. At the end of the second quarter, Bloom had nearly $2.7 billion in cash on its balance sheet. The company is generating $175 million in free cash flow. Finally, Bloom's agreements with Brookfield and Industrial Development Funding help absorb funding risk, allowing it to scale without fears of dilution through equity or debt offerings.
BE Revenue (TTM) data by YCharts
What's next for Bloom Energy
Over the next couple of years, investors will want to see Bloom deliver on its massive hyperscaler deals and prove it can manufacture and deliver solid-oxide fuel cells on time and at scale. Bloom has passed its first test with its initial customers and has proven it can deliver power quickly. Now it's time to scale up and potentially secure even more major deals.
To support this, Bloom is developing and marketing its 800V DC-native energy server platform. This platform will connect DC-native power to DC-native compute, cutting out the middleman and reducing energy waste for hyperscalers. Bloom estimates that this can cut non-computer capital expenditures for a 1 GW data center by $3.6 billion, or 27%.
Bloom will begin deploying early versions of its DC-native platform next year and will expand and retool manufacturing to produce them at scale for data center customers. The Open Compute Project and major semiconductor developers aim to have 800V DC as the default standard by 2028. By 2030, Bloom hopes its energy servers will become the standard for behind-the-meter campuses.
Execution will determine Bloom Energy's future
Bloom Energy has benefited from rising data center power demand, and its backlog stands at $442 million, with management noting that backlog growth is outpacing revenue growth.
However, even after a recent drop, Bloom stock is not cheap, at roughly 40 times forward earnings. This high valuation reflects robust growth, leaving Bloom's stock vulnerable to price volatility. But if it can continue expanding manufacturing capacity, deliver on its massive deals, and generate strong free cash flow, Bloom could deliver strong returns over the next five years.
SummaryColumbia Banking System is rated BUY, offering a 5% yield and a $1.2 billion share buyback, supporting a compelling risk/reward profile.COLB's 3Q26 results exceeded expectations, with NIM above 4%, strong credit quality, and efficiency ratio at 51.34%, outperforming industry benchmarks.The Pacific Premier Bancorp acquisition expands COLB's geographic reach and is expected to be mid-teens EPS accretive, enhancing commercial relationships and non-interest income.Shares trade at a 20% discount to sector median P/B, with higher forward ROE and robust capital ratios, providing both income and growth appeal. J Studios/DigitalVision via Getty Images
Summary Columbia Banking System, Inc. (COLB) is rated a BUY. The stock is yielding 5% compared to the financial sector median of 2.8%. In addition, management just announced a $1.2 billion share buyback. 3Q26 results were stronger than expected, where
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Analyst’s Disclosure: I/we have no stock, option or similar derivative position in any of the companies mentioned, and no plans to initiate any such positions within the next 72 hours. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.
Seeking Alpha's Disclosure: Past performance is no guarantee of future results. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. Any views or opinions expressed above may not reflect those of Seeking Alpha as a whole. Seeking Alpha is not a licensed securities dealer, broker or US investment adviser or investment bank. Our analysts are third party authors that include both professional investors and individual investors who may not be licensed or certified by any institute or regulatory body.
Akcie Carpenter Technology tento týden klesly o 24,5 % poté, co tržby za 1. čtvrtletí fiskálního roku 2027 ve výši 798,2 mil. USD nedosáhly očekávaných 830,8 mil. USD.
A quarterly revenue report that missed Wall Street expectations sent Carpenter Technology (CRS -2.60%) tumbling 22.5% this week, overshadowing an earnings beat.
Carpenter Technology stock changed hands at $292.26 as of the close on Friday, Oct. 23, down 24.5% this week from Friday, Oct. 16's close, according to data provided by S&P Global Market Intelligence. Over the same period, the S&P 500 (^GSPC -0.52%) was flat, and the Nasdaq-100 was down 0.8%.
Image source: Getty Images.
A revenue miss overshadows record marginsThe company reported first-quarter fiscal 2027 sales of $798.2 million, up 8.8% year over year from $733.7 million but below Wall Street consensus estimates of $830.8 million. Diluted earnings per share reached $3.25, topping analyst expectations of $3.04. "The sequential sales decline was driven by the planned maintenance outages we discussed on the last earnings call," CEO Tony R. Thene said on the conference call. The sharp sell-off leaves the stock down 54.5% (as of the close on Friday, Oct. 23) from its 52-week high of $625.99.
Carpenter Technology manufactures high-performance specialty metals and alloys for aerospace, defense, and medical customers needing materials that withstand extreme heat and pressure. Demand in its core markets remains solid, evidenced by a 49% year-over-year jump in order bookings across aerospace structural and distribution sub-markets.
Management reaffirmed its full-year operating income guidance of $850 million to $880 million and authorized a new $1 billion share buyback program. A top-line revenue miss despite record margins sharpens the tension between Carpenter's valuation and its ability to maintain rapid sales growth.
What's next for Carpenter TechnologyInvestors will watch for sales recovery when the company reports its next quarterly results on Feb. 4, 2027. The industrials stock trades at a trailing price-to-earnings (P/E) ratio of 25.1, a level that leaves little room for operational delays or missed revenue expectations.
While many seem to believe that Carpenter Technology stock isn't helping them to build a better portfolio right now, they are clearly overreacting. Sure, the company's failure to meet analysts' revenue expectations is disappointing, but it's hardly a red flag that suggests Carpenter Technology stock is a sell. Analysts are hardly perfect, and a company's inability to meet analysts' expectations is forgivable when it simultaneously achieves so many successes as Carpenter Technology recently did.
Those reluctant to click the buy button now because of the stock's 25.1 P/E ratio should recognize that, with respect to operating cash flow, Carpenter Technology stock is a bargain, trading at 17.9 times operating cash flow compared to its five-year average cash flow multiple of 19.3.
Scott Levine has no position in any of the stocks mentioned. The Motley Fool has positions in and recommends Carpenter Technology. The Motley Fool has a disclosure policy.
There's an easy sales pitch for software that can help organizations run their vehicles and equipment more effectively: Show clients how the product can save time or money. Samsara (IOT +2.60%) does just that, helping to bridge the gap between operational data and software.
Artificial intelligence (AI) can make these tools even more productive, but greater productivity alone doesn't make an investment thesis. For investors looking ahead to 2027, the real question is whether Samsara can turn its potential into fundamental growth that exceeds the expectations embedded in its stock. If it can, it's possible that this under-the-radar stock could soar, perhaps even matching the run of Palantir, a stock that skyrocketed more than 700% during the past five years. Let's dig in and see how realistic that scenario is.
Image source: Getty Images.
What Samsara actually does To understand Samsara's business, we must follow a hypothetical example. Imagine a factory. Tens of thousands of moving parts and hundreds of workers are hard at work, focused on the task at hand. There's one problem: A key piece of equipment is at risk of failure. Worse, this type of failure wouldn't just cause downtime; it could also pose a health and safety risk. Samsara's software is designed to catch these issues before they become critical. It keeps operations running smoothly, saves money, and protects key assets.
The company operates on a "land-and-expand" model. It sells its product platform once, then collects recurring revenue from clients. A key aspect of its business model is upselling -- selling additional modules to existing customers to generate more revenue.
IOT Samsara$44.92+$1.14 (+2.60%)
NYSE · As of 4:00 PM ET 10/23/26
Can 2027 be Samsara's breakout year? As for fundamentals, they've taken off recently. Samsara's revenue has increased from about $250 million in 2021 to more than $1.84 billion during the past 12 months. Free cash flow has also increased, swinging from about $150 million in cash burn in 2023 to $255 million in free cash flow during the past 12 months. What's more, the company recently turned the corner on profitability, generating about $91 million in net income during the past year.
Although these metrics are encouraging, Samsara will need to go further in 2027 for its stock to truly take off. The company recently noted that roughly 96% of its customers with more than $100,000 in annual recurring revenue (ARR) now use at least two of its products, and 70% use three or more. If the company can increase those numbers further while expanding its existing customer base, the stock market could take notice.
Is Samsara's valuation its final hurdle? If one factor is holding Samsara back, it could be its valuation. On a price-to-earnings (P/E) ratio basis, its stock trades at about 290. Granted, that is very high. However, Samsara is a young company that has only recently begun producing consistent profits. Therefore, the "E" (earnings) in the equation remains very modest. Consequently, it may be better to examine Samsara's price-to-sales (P/S) ratio instead.
IOT P/S Ratio data by YCharts.
As you can see, Samsara's P/S ratio tells a more nuanced story. While 13.5 is high compared to much of the stock market, it's still reasonable compared to its past readings. In fact, Samsara stock is currently trading for less than its lifetime average P/S ratio of 16.5. Nevertheless, these valuations underscore that Samsara will need to deliver more profit to lower its P/E multiple to levels that will attract more institutional interest.
Is Samsara a buy now? Samsara is a stock worth considering for growth-oriented investors with a bullish outlook on AI's impact on real-world operations. However, the stock still has challenges. Its margins remain thin, and it lacks a long history of consistent profitability. Therefore, the stock isn't for every investor.
Yet improving fundamentals, led by soaring revenue and free cash flow, point to a key tailwind: Organizations are beginning to view AI tools as a recurring operating expense. That bodes well for Samsara. Investors willing to buy and hold the stock could be rewarded in the long run, perhaps as soon as 2027.
FTC zažalovala společnost Hims & Hers kvůli údajnému sdílení citlivých zdravotních údajů a klamavým praktikám; akcie HIMS 29. července 2026 klesly o 14,73 % na 25,00 USD.
Faruqi & Faruqi, LLP Securities Litigation Partner James (Josh) Wilson Encourages Investors Who Suffered Losses In Hims To Contact Him Directly To Discuss Their Options
If you purchased or acquired securities in Hims between August 4, 2025 and July 29, 2026 and would like to discuss your legal rights, call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983-9330 (Ext. 1310).
[You may also click here for additional information]
New York, New York--(Newsfile Corp. - October 25, 2026) - Faruqi & Faruqi, LLP, a leading national securities law firm, is investigating potential claims against Hims & Hers Health, Inc. (""Hims" or the "Company") (NYSE: HIMS) and reminds investors of the November 2, 2026 deadline to seek the role of lead plaintiff in a federal securities class action that has been filed against the Company.
Faruqi & Faruqi is a leading national securities law firm with offices in New York, Pennsylvania, California and Georgia. The firm has recovered hundreds of millions of dollars for investors since its founding in 1995. See www.faruqilaw.com.
As detailed below, the complaint alleges that the Company and its executives violated federal securities laws by making false and/or misleading statements and/or failing to disclose that: (1) the Company shared consumers' health information with third-party advertising platforms; (2) the Company charges consumers for prescriptions almost immediately after they submit an intake form, despite telling consumers that they will be able to consult with a medical provider to find a treatment that is "right for them;" (3) the foregoing conduct subjected the Company to regulatory scrutiny; (4) as a result of the foregoing, the Company was reasonably likely to incur fees and penalties; and (5) as a result of the foregoing, Defendants' positive statements about the Company's business, operations, and prospects were materially misleading and/or lacked a reasonable basis.
On July 29, 2026, during market hours, the Federal Trade Commission announced it had filed a lawsuit against Hims "alleging that the telehealth provider shared consumers' sensitive health information about medical conditions with third-party advertising platforms despite claiming its services maintain consumers' privacy and deceives users about its billing and cancellation practices." On this news, Hims's stock price fell $4.32, or 14.73%, to close at $25.00 per share on July 29, 2026, on unusually heavy trading volume.
The court-appointed lead plaintiff is the investor with the largest financial interest in the relief sought by the class who is adequate and typical of class members who directs and oversees the litigation on behalf of the putative class. Any member of the putative class may move the Court to serve as lead plaintiff through counsel of their choice, or may choose to do nothing and remain an absent class member. Your ability to share in any recovery is not affected by the decision to serve as a lead plaintiff or not.
Faruqi & Faruqi, LLP also encourages anyone with information regarding Hims's conduct to contact the firm, including whistleblowers, former employees, shareholders and others.
To learn more about the Hims class action, go to www.faruqilaw.com/HIMS or call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983-9330 (Ext. 1310).
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Frequently Asked Questions (FAQ) for Investors Regarding the Hims Securities Class Action Lawsuit:
What is the Hims securities fraud lawsuit about?
Faruqi & Faruqi, LLP has filed a securities class action lawsuit alleging that Hims & Hers Health, Inc. (NYSE: HIMS) made materially false and misleading statements to investors during the Class Period. The complaint alleges that the Company shared consumers' sensitive health information with third-party advertising platforms despite representing that its services maintain consumer privacy, and that the Company allegedly charged consumers for prescriptions almost immediately after intake form submission while telling consumers they would first be able to consult with a medical provider. The lawsuit further alleges that this conduct subjected Hims to regulatory scrutiny and made the Company reasonably likely to incur fees and penalties. On July 29, 2026, the Federal Trade Commission announced it had filed a lawsuit against Hims alleging these practices, and on that news Hims's stock price allegedly fell $4.32, or approximately 14.73%, to close at $25.00 per share on unusually heavy trading volume. As a result of the foregoing, the complaint alleges that Defendants' positive statements about the Company's business, operations, and prospects were materially misleading and/or lacked a reasonable basis.
Who may be eligible to participate in the lawsuit?
Investors who purchased or otherwise acquired securities of Hims & Hers Health, Inc. (NYSE: HIMS) on the NYSE exchange between August 4, 2025 and July 29, 2026, inclusive, may be eligible to participate in this class action lawsuit. Eligibility to participate in any potential recovery is not limited to investors who seek appointment as lead plaintiff; any investor who purchased Hims securities during the Class Period may be a class member. Eligible investors are encouraged to review their trading records to determine whether their purchases fall within the defined Class Period. Investors with questions about their eligibility may wish to consult with counsel to better understand their rights and options in connection with this litigation.
What is a lead plaintiff, and how can I seek appointment?
A lead plaintiff is a court-appointed representative who serves on behalf of all class members and plays an active role in directing the litigation, including working with counsel on case strategy and settlement decisions. Any investor who purchased Hims securities during the Class Period and suffered a loss may move the court for appointment as lead plaintiff, provided that motion is filed no later than November 2, 2026. Courts typically appoint the investor or group of investors with the largest financial interest in the litigation who also satisfy the requirements of Federal Rule of Civil Procedure 23 as lead plaintiff. Importantly, an investor need not seek appointment as lead plaintiff in order to participate in or share in any recovery that may result from the litigation. Investors who do not seek lead plaintiff status retain the right to remain members of the class and benefit from any judgment or settlement.
Why should investors contact Faruqi & Faruqi, LLP?
Faruqi & Faruqi, LLP has represented investors in securities litigation for decades and has recovered hundreds of millions of dollars for shareholders. Investors who purchased Hims securities during the Class Period may contact the firm to discuss their legal rights, potential claims, and the lead plaintiff process at no cost or obligation.
Attorney Advertising. The law firm responsible for this advertisement is Faruqi & Faruqi, LLP (www.faruqilaw.com). Prior results do not guarantee or predict a similar outcome with respect to any future matter. We welcome the opportunity to discuss your particular case. All communications will be treated in a confidential manner.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/320646
Source: Faruqi & Faruqi LLP
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Elon Musk just promised millions of people a gift. On Monday, the co-founder and CEO of Tesla (TSLA -0.63%) and Space Exploration Technologies (SPCX +1.89%) wrote in a post at X -- the social media platform formerly known as Twitter -- "Next year, I will give one of my SpaceX shares to every kid in America." He then added, "This will be the first of many."
It sounds good, particularly if you're one of those children about to receive the gift. But what will it cost, and who pays other than Musk?
Musk didn't add any other details. We can, however, make some reasonable assumptions about how this will work.
More than enough already in hand
Musk doesn't need to dilute existing shareholders by issuing new shares of SPCX to make good on his gift. Musk himself effectively controls or personally owns 6.4 billion A shares of the recently public company, in addition to 3.9 billion B shares. There's another 1.3 billion restricted B shares that could soon become his as well, plus 350 million more that he could purchase if he chooses to exercise his options.
For comparison, there are currently just over 72 million children under the age of 18 residing in the United States, according to The Annie E. Casey Foundation. Assuming Musk is using the same standard about who qualifies as a kid, he could give away a mere 1.8% of the 3.9 billion B shares he already owns and still fulfill his promise.
SpaceX and Tesla CEO Elon Musk. Image source: The White House.
His total net cost? At today's price, that's roughly $12 billion worth of SPCX stock, which, of course, is only a fraction of his estimated net worth of right around $1 trillion right now.
And it's almost certainly SpaceX's B shares that Musk intends to give away. Although he personally owns just a little less than half of the company, the A shares' voting power is 10 times that of B shares, effectively giving Musk 85% control of Space Exploration Technologies. He's not apt to give any of that up.
Barely a blip
As for what it means to every other SPCX shareholder, the answer is not a lot... at least not initially. Musk can personally afford to fund the entirety of this gift. No dilution is necessary.
Longer-term, though, there is a slight conceivable impact. This will put a single share of SpaceX stock in 72 million different investors' hands, with little clarity as to how or even whether selling it will be restricted. Hopefully, most of these recipients will hang onto it indefinitely and use it as a seed for a retirement nest egg. Many of them will likely sell it at their first opportunity, however.
Fortunately, nearly 100 million shares of SPCX trade hands every single day. The market should be able to absorb such a disruption without too much turmoil.
Akcie Alphabet třídy C (GOOG) se obchodují přibližně o 1 % níže než hlasovací akcie třídy A (GOOGL), přestože mají stejná práva na dividendy a podíl na zisku.
Buying Alphabet (GOOGL -1.24%)(GOOG -1.08%) stock gives you a choice most stocks don't offer. The Google parent has two classes of common shares on the Nasdaq. Its Class A shares trade under the ticker GOOGL, and its Class C shares trade as GOOG.
As of this writing, the Class A stock is around $335 and the Class C stock about $331. That puts the voting class about 1% higher. And the extra cash buys only one thing: a vote.
Anyone buying Meta Platforms stock will soon have the same choice. On Oct. 21, the social media company said it plans to add a non-voting Class C stock of its own, starting Jan. 19, 2027.
Image source: Getty Images.
What's a Class A vote worth?Technically, Alphabet has three classes of common stock. Class A shares carry one vote apiece. Class B shares, which don't trade publicly, carry 10 votes each. And Class C shares carry no votes at all, except when the law requires one.
Everything else is the same.
In its latest quarterly filing, Alphabet said the rights of its Class A, Class B, and Class C holders, "including the liquidation and dividend rights," are identical other than voting. Not only do all three classes get the same 22-cent quarterly dividend, but every share also has the same claim to Alphabet's net income.
What counts more is who owns the Class B shares. As of April 6, co-founders Larry Page and Sergey Brin together had around 53% of Alphabet's total voting power, according to the company's latest proxy statement.
Alphabet's annual report says the stake gives them the ability to elect all its directors and decide most issues put to a shareholder vote. It adds that handing out non-voting Class C stock, including as employee pay, can help keep the founders' share of the vote the same.
Put another way, as long as their stake stays over half, the founders can outvote all other shareholders combined. For an everyday investor, I think that leaves the Class A vote nearly symbolic.
A shifting gapThe 1% gap isn't a constant, either. A year ago, the Class A stock traded just below the Class C stock.
In fact, from 2020 through 2025, the non-voting shares usually cost a bit more. Class C closed above Class A every trading day in 2023 and 2024. Class A only moved ahead again this spring, and its premium has sat near 1% since September.
A likely reason is that Alphabet itself had been a huge buyer of its Class C stock. From 2023 through 2025, the company spent about $142 billion repurchasing Class C shares, versus about $28 billion on Class A shares. It chose between the two partly on "the relative trading prices and volumes" of each class, according to its annual report.
Then the buying ended. Alphabet repurchased no shares of either class in the first half of 2026, a stretch in which it sold new stock and borrowed a lot as it stepped up its artificial intelligence (AI) build-out.
Notably, when Alphabet sold new stock in June, it sold equal amounts of both classes -- 29 million Class A shares for around $355 each and 29 million Class C shares for about $352. That, too, was a gap of about 1%.
GOOGL Alphabet$320.21-$4.01 (-1.24%)
NASDAQ · As of 4:00 PM ET 10/23/26
Class C is the better buyPaying more for the Class A shares makes sense mostly for investors who want a say in how Alphabet is run. With the founders holding a majority of the vote, I don't think that say matters much now.
The discount on Class C, though, means buying the same business at a slightly lower valuation. For a $10,000 investment, picking Class C over Class A buys around a third of a share more -- about $114 worth of extra stock in the same business. And whatever Alphabet reports on Wednesday, Oct. 28, when it posts its third-quarter results, both classes share in it equally.
Of course, the gap might keep growing, and anybody buying Class C now would lag Class A holders by the difference. But the gap has held within around 2% in either direction since 2022. And if Alphabet resumes buying back Class C stock, the gap might shrink in Class C holders' favor.
Which class would I buy, then? I'd pick the Class C shares.
I think Alphabet is a top stock to buy either way. But I don't see a reason to pay about 1% more for a vote that, for now, doesn't change much.
Amazon (AMZN -0.95%) has been a poor stock to own recently. While it rose following its Q2 earnings release, the stock has slowly sold off since then and is now up about 8% for the year, trailing the S&P 500 (^GSPC -0.52%). However, I think this could all turn around once again after Oct. 29, when Amazon reports Q3 earnings.
The reason is fairly clear, and investors have already seen it cause Amazon's price tag to spike once already this year: cloud computing growth.
Image source: The Motley Fool.
Amazon is the industry leader in cloud computing
Amazon may not be the first name you think of when discussing huge tech companies, but it should be high on the list. While most consumers are familiar with Amazon's commerce site and delivery platform, Amazon Web Services (AWS) really steers the business. In fact, AWS -- which supplies cloud computing -- accounted for 60% of Amazon's operating income in Q2, despite making up only 21% of revenue.
How? AWS's operating margins are far superior to those of its commerce business, which is a notoriously razor-thin-margin industry.
While commerce still affects Amazon's investment picture, investors must realize that Amazon doesn't care much about it right now. Amazon is spending about $220 billion this year to expand its computing infrastructure and fuel AWS growth. It seems content with its current dominance in commerce and sees a major opportunity in cloud computing right now, thanks to booming demand for running AI workloads.
AMZN Amazon$248.00-$2.38 (-0.95%)
NASDAQ · As of 4:00 PM ET 10/23/26
These investments have so far paid off, as AWS's growth rate has significantly climbed over the past few quarters. Rewinding to Q4 2025, AWS's growth was 24% year over year. Then it accelerated to 28% in Q1 2026. Amazon surprised investors by reporting impressive 37% growth in Q2, which caused shares to skyrocket earlier this year before eventually selling off.
If Amazon continues to meaningfully accelerate its AWS growth rate, say to the mid-40% range, it could ignite another run-up in stock price, as it would have a positive effect on Amazon's operating margins. This, in turn, will cause earnings per share to rise faster, which the market will love.
If it can do that, Amazon's stock should be primed to rise, because it's actually pretty reasonably valued right now, at least compared to historical levels.
Amazon's stock isn't that expensive
Valuing Amazon's stock is a bit tricky. While the price-to-earnings (P/E) ratio is the gold standard for valuing stocks like Amazon, it's currently not applicable.
Amazon has been a major investor in private company Anthropic, whose valuation has risen substantially over the past year. Accounting rules require Amazon to report these investment gains as profits, even if it hasn't sold them yet. So, Amazon has a lot of profits on paper, but not as many in real life.
To adjust for this, I value Amazon on its operating income, which is one line item above net income. This metric doesn't account for gains on investment, taxes, depreciation, or other factors that could skew the results. It's just how the business itself is doing. From this standpoint, Amazon's price-to-operating-income ratio has declined substantially over the past few years.
AMZN Operating PE Ratio data by YCharts
While it has been slightly cheaper a handful of times this year, it is still pretty reasonably valued. I think now is the perfect time to load up on shares, as its valuation could increase following strong Q3 results likely be highlighted by impressive AWS growth.
I'm bullish on Amazon's future, and AWS will be the division that takes it to the next level as an investment.
Microsoft ve fiskálním roce 2026 zvýšil tržby o 18 % na 331,8 mld. USD, ale volný peněžní tok klesl o 6 % na zhruba 67 mld. USD v důsledku kapitálových výdajů.
Microsoft (MSFT +0.66%) closed at a record $543.45 on Oct. 13, and it hasn't moved far since. Shares trade near $530 as of this writing, about 2% off the high. Microsoft posts results for the fiscal first quarter of 2027 (the three months ended Sept. 30, 2026) after the market closes on Wednesday, Oct. 28.
The company has earned a good chunk of that climb. Microsoft's adjusted earnings per share jumped 22% for fiscal 2026, which ended June 30.
But at today's price, shares cost about 31 times those earnings. It's a steep price for a business whose own guidance suggests slower growth right as its capital spending keeps rising.
I'd buy the stock at about $465 a share, roughly 12% under where it trades now.
Image source: Getty Images.
A strong year, already paid forMicrosoft's fiscal 2026 was impressive by nearly any measure. Revenue grew 18% to $331.8 billion, and operating income climbed 21% to $155.2 billion. Non-GAAP (adjusted) earnings per share, which strip out the effect of Microsoft's investments in OpenAI, increased 22% to $17.28. And the pace held up all year, with adjusted earnings per share up 23% year over year in both the first and fourth quarters of fiscal 2026.
But the stock price already reflects much of that. With shares around $530, Microsoft trades at about 31 times its fiscal 2026 adjusted earnings. On reported earnings of $17.95 per share, it's about 30.
The price-to-earnings ratio for the S&P 500 (^GSPC -0.52%) on its reported earnings is about 26. The premium is easier to defend when earnings rise 22% a year.
Growth is cooling as spending climbsAnd management's forecast for the September quarter suggests growth is slowing, at least a little. Microsoft sees revenue between $89.85 billion and $90.95 billion, cost of revenue between $29.6 billion and $29.8 billion, and operating expenses between $16.8 billion and $16.9 billion. At these levels, operating income would climb around 14% to 17% from the year-ago quarter's $38.0 billion. This compares to year-over-year growth of 24%, 21%, 20%, and 18% over the four quarters of fiscal 2026.
In short, operating income growth has slowed every quarter for a year, and the guidance shows it slowing again.
The spending is the bigger reason I want a discount. Cash from operations grew a strong 34% in fiscal 2026, to about $183 billion. But Microsoft also spent almost $116 billion on additions to property and equipment, so free cash flow dipped about 6% to roughly $67 billion.
What's more, management expects capital expenditures of about $175 billion in calendar 2026.
"[W]e expect to remain free cash flow positive in FY27," chief financial officer Amy Hood said on Microsoft's earnings call in July.
It's arguably a low bar -- Microsoft produced around $67 billion in free cash flow last fiscal year.
Why $465?My buy price starts with the $17.28 Microsoft earned per share last fiscal year on an adjusted basis. I'd pay a price-to-earnings multiple of around 27 on that number, which comes out to about $465 a share.
At that price, Microsoft's price-to-earnings ratio on reported earnings would be about 26, on par with the S&P 500's. I think paying around the market's valuation multiple is fair for a business whose earnings growth looks set to cool toward the mid-teens as its spending keeps climbing. Shares last closed under $465 on July 31, two days after the company's fiscal fourth-quarter report pushed the stock sharply higher.
The Oct. 28 report might shift my price in two ways. The first is earnings. Because my price is linked to trailing adjusted earnings per share, every strong quarter lifts it.
MSFT Microsoft$524.51+$3.43 (+0.66%)
NASDAQ · As of 4:00 PM ET 10/23/26
Management's guidance suggests operating income growth of a bit over 15% at the midpoint. If adjusted earnings per share gained 15% from the year-ago period's $4.13, trailing adjusted earnings per share would reach around $17.90, and my buy price would rise to about $483.
The second is Azure, Microsoft's cloud computing platform. As I wrote earlier this month, I think the stock needs Azure's growth to stay above 40%. If Azure falls short, or if free cash flow keeps dropping, I'd want to pay a lower price-to-earnings ratio than 27, and my buy price would fall with it.
Would I buy Microsoft stock before Oct. 28? Not at roughly $530.
Sure, a strong report might raise my buy price, and shares may never drop as low as $465. But at about 31 times adjusted earnings, I think the stock already reflects most of the good news. I'd consider buying closer to $465.
Most of the attention on Berkshire Hathaway (BRKA -0.84%) (BRKB -0.87%) owes to its impressive investment portfolio. But Berkshire Hathaway stock is also worth watching on its own, and its shares did something this month that it hasn't accomplished in eight years.
The conglomerate, now led by Greg Abel after the retirement of its longtime leader, Warren Buffett, saw its Class B shares close higher for 10 consecutive trading sessions from Oct. 1 through Oct. 14. Berkshire's stock rose from about $498 to $526.
Berkshire snapped the streak on Oct. 15, but the stock is on another run higher, recently topping $547 and beating the record close of $539.89 set in May 2025.
Obviously, it's a great time to be a Berkshire Hathaway investor. But let's also look at the bigger picture about what happens when Berkshire stock goes on a 10-day winning run. This has happened only six other times since 1998 -- and in four of those six instances, the shares were trading higher 12 months later.
Does that mean investors should buy Berkshire stock today? History offers some encouragement, but there's a much stronger argument for owning Berkshire than its recent winning streak.
Image source: Getty Images.
What does a Berkshire winning streak mean?
Berkshire's earlier streaks of at least 10 consecutive higher closes occurred in 1998, 2003, 2014, twice in 2017, and in January 2018.
The longest came in August 2017, when the shares advanced for 15 consecutive sessions. Berkshire also recorded another extended winning streak in March of that year.
Let's be clear -- although it's a bullish signal that Berkshire posted 12-month gains on four separate occasions after those 10-day runs, that doesn't guarantee that the stock will be higher one year from now. After all, six previous occurrences are a small sample size.
The historical results suggest that an extended winning streak isn't automatically a warning that investors have missed their opportunity. But a 67% success rate doesn't establish that Berkshire has a two-thirds chance of rising during the next year.
Fortunately, investors have something more useful than historical trading patterns to help them make that decision.
$542.19-$4.78 (-0.87%)
NYSE · As of 4:00 PM ET 10/23/26
Berkshire has plenty going for it
One of the biggest questions surrounding Berkshire entering 2026 was how the company would perform after Buffett's retirement as chief executive officer.
So far, Abel has demonstrated that he's willing to put Berkshire's enormous financial resources to work.
Berkshire doubled down on its position in Alphabet, the parent company of Google, while also adding to positions in companies such as Delta Air Lines. The company has also resumed substantial share repurchases, buying back about $4.4 billion of its own stock.
The buybacks are a signal to investors -- Berkshire has always been cautious about buying its own stock and has a stated philosophy of buying only when the stock is trading below its intrinsic value.
Of course, a buyback isn't proof that Berkshire shares are undervalued today, particularly after their recent advance. But it's an encouraging indication of management's willingness to deploy capital when opportunities arise.
And Berkshire still has considerable financial flexibility. Its cash reserves provide ample flexibility for Abel to make acquisitions, invest in more companies, or buy back more of the company's own shares.
Meanwhile, Berkshire's collection of operating businesses, including insurance, railroads, utilities, and manufacturing operations, gives investors exposure to several important parts of the economy without having to purchase individual stocks.
That's a compelling combination for long-term investors.
Is Berkshire Hathaway stock a buy now?
There's another reason I like Berkshire that has little to do with its October winning streak.
Historically, Berkshire has demonstrated an ability to hold up relatively well during difficult markets. In fact, Berkshire outperformed the S&P 500 in 11 of the 13 calendar years when the index posted a negative return.
That doesn't mean Berkshire is immune to market declines. But its diversified businesses, financial resources, and disciplined approach to investing can make it an attractive long-term holding.
And that's where the historical winning-streak data becomes less important.
Berkshire's 10 consecutive gains this month -- or in any year -- don't guarantee positive returns 12 months from now, particularly with the shares trading at a record high. Investors buying today also need to recognize that a strong business isn't automatically an attractive investment at any price.
But I remain bullish on Berkshire's long-term prospects under Abel. The company's financial strength, diverse operations, and renewed willingness to deploy capital provide several avenues to reward shareholders over time.
The October winning streak may have caught Wall Street's attention. For long-term investors, though, Berkshire's underlying business is a much better reason to own the stock.
Palantir očekává v roce 2026 tržby ve výši 8,15 mld. USD; podle odhadů by ve zprávě za druhé čtvrtletí 2027 mohl dosáhnout hranice 10 mld. USD v tržbách za předchozí čtyři čtvrtletí.
Shares of Palantir Technologies (PLTR +0.28%) ended at a record $209.05 on Oct. 9. At roughly $198 as I write, they're about 5% under that peak.
The artificial intelligence (AI) software specialist's second-quarter revenue grew 93% year over year to about $1.94 billion. And management now expects about $8.15 billion in revenue for 2026, or 82% more than last year.
At this rate, a $10 billion year isn't far away. Palantir's revenue for its past four quarters could clear that level as early as the middle of 2027.
My prediction: when it does, Palantir stock will trade at roughly $208, almost exactly where it set its record. That'd be just about 5% above today's price, though Palantir would be taking in about 60% more revenue a year than it did in its past four reported quarters.
Image source: Getty Images.
When does Palantir reach $10 billion?Palantir's growth has sped up for four straight quarters. Revenue climbed 48% year over year in the second quarter of 2025, then 63% in the third quarter, 70% in the fourth quarter, 85% in the first quarter of 2026, and 93% in the second quarter. Net income grew even faster, more than tripling year over year to around $1.06 billion in the second quarter.
Management's guidance, though, calls for growth to slow from here. Palantir sees third-quarter revenue of around $2.16 billion, or about 83% growth. And its full-year outlook implies fourth-quarter revenue of around $2.42 billion, up about 72%. Then again, Palantir has tended to beat its own forecasts. In each of the past three quarters, revenue landed around 6% to 8% above the top of management's range.
Plus, the full-year target keeps rising. It went from around $7.19 billion in February to about $7.65 billion in May, then to around $8.15 billion in August.
If the third and fourth quarters match guidance, Palantir's trailing revenue reaches $10 billion when its first-half 2027 sales rise around 52% year over year. If those two quarters beat guidance by about as much as the past three did, growth in the mid-40s would do it.
Either way, the milestone would probably show up in Palantir's second-quarter 2027 report.
Investors are paying less for each dollar of salesPalantir's market value of around $477 billion comes out to about 77 times its revenue in the past four reported quarters. A year ago, the price-to-sales multiple was about 128 times sales. The sales multiple fell by around 40% in a stretch when revenue growth almost doubled.
Put simply, investors paid a bit more for the business overall but far less for each dollar it took in. The shares gained around 7% in that year, while trailing revenue grew about 79%.
I'll assume the sales multiple keeps falling at about that rate, hitting 50 times sales by the middle of 2027. Fifty times sales is still a rich price for any software company. But I think it's a fair one for a business that, if guidance holds, would be growing slower than it is now.
The stock could end up right back at its recordAt 50 times sales, $10 billion of yearly revenue supports a market value of about $500 billion. Divide it by the 2.4 billion shares Palantir reported outstanding in its last quarterly filing, and you get about $208 a share.
From today's price of roughly $198, that is a return of about 6% a year, if the stock gets there around August 2027.
PLTR Palantir Technologies$196.75+$0.56 (+0.28%)
NASDAQ · As of 4:00 PM ET 10/23/26
That estimate also fits with the price where I'd consider buying Palantir stock -- about $140, or about 120 times its earnings in the last year. If Palantir keeps turning about half its revenue into net income, as it did in the past four quarters, $208 would be about 110 times earnings by mid-2027.
In that case, the stock would be cheaper by my measure than it is now, even at a slightly higher price.
The bigger risk is that the sales multiple falls faster than I think, if growth slows more sharply than guidance implies. The stock shed around 34% of its value over the first half of 2026 alone. And that risk is why 6% a year looks thin to me.
The company could reach $10 billion within a year or so. But at about $198, I think investors are already paying for most of that growth. I'm happy to let the revenue catch up with the price first.
Longer-term data reflecting nearly 4 years of follow-up show a further reduction in the risk of death from 14% to 37% for those initially treated with Libtayo, despite an 88% crossover from the placebo arm upon recurrence
New prospective analyses confirm sustained disease-free survival (DFS) benefit with adjuvant Libtayo, including in patients who are minimal residual disease (MRD) negative at baseline
The late-breaking data were presented during a rapid oral session at the European Society for Medical Oncology (ESMO) 2026 Meeting
TARRYTOWN, N.Y., Oct. 25, 2026 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced longer-term data reflecting nearly four years of follow-up from the Phase 3 C-POST trial evaluating PD-1 inhibitor Libtayo® (cemiplimab) as adjuvant treatment for patients with cutaneous squamous cell carcinoma (CSCC) at a high risk of recurrence after surgery and radiation. The late-breaking results were presented in a rapid oral session at the European Society for Medical Oncology (ESMO) Congress 2026.
“As the Phase 3 C-POST trial data continue to mature, we are seeing an evolving and clinically meaningful overall survival benefit with adjuvant Libtayo in high-risk cutaneous squamous cell carcinoma, as well as sustained disease-free survival benefit regardless of whether minimal residual disease is detectable at baseline,” said Danny Rischin, M.D., M.B.B.S., F.R.A.C.P., Research Lead, Head and Neck Cancer and Cutaneous SCC, Department of Medical Oncology at the Peter MacCallum Cancer Centre in Melbourne, Australia, and lead investigator of the trial. "These data provide compelling evidence of the long-term, durable benefit of adjuvant treatment with Libtayo in high-risk CSCC after surgery and radiation, further supporting Libtayo as a transformative standard of care for these patients."
With a median follow-up of 44 months, efficacy results for Libtayo compared to placebo showed sustained benefits for the primary endpoint of disease-free survival (DFS), and notably, an increasing overall survival (OS) benefit, a secondary endpoint. Specifically, there was a 37% reduction in the risk of death (hazard ratio [HR]: 0.63; 95% confidence interval [CI]: 0.36-1.11) at a median follow up of 44 months, up from 22% at a median follow up of 30 months (HR: 0.78; 95% CI: 0.39-1.56) and 14% at a median follow up of 24 months (HR: 0.86; 95% CI: 0.39-1.90). Notably, patients randomized to placebo were able to cross over to Libtayo after recurrence, and 61 of 69 placebo patients (88%) with recurrence received subsequent Libtayo. The emerging OS benefit, despite the high crossover rate, therefore supports treating high-risk patients with Libtayo after surgery and radiation, rather than waiting for their disease to recur.
Additionally, an exploratory analysis of patients with baseline circulating tumor DNA (ctDNA) data (Libtayo n=93; placebo n=98) was conducted. Compared to placebo, treatment with adjuvant Libtayo improved DFS regardless of baseline minimal residual disease (MRD) status, supporting the broad clinical utility of adjuvant Libtayo in high-risk CSCC. In particular, patients who were MRD negative at baseline – and thus had lower risk of recurrence – still had improved DFS with Libtayo (HR: 0.45; 95% CI: 0.22-0.95); patients who were MRD positive at baseline also had improved DFS with Libtayo (HR: 0.24; 95% CI: 0.07-0.86).
Safety results remained consistent with previously reported data. Treatment emergent adverse events (TEAEs) of any grade occurred in 94% of patients in the Libtayo arm and 91% of patients in the placebo arm. Grade ≥3 TEAEs occurred in 26% of patients (Libtayo) and 17% of patients (placebo). Treatment discontinuations due to TEAEs occurred in 10% of patients (Libtayo) and 3% of patients (placebo). TEAEs leading to death occurred in 2% of patients in each arm.
The longer-term C-POST data at ESMO expand on results shared at the 2025 ASCO Annual Meeting and simultaneously published in the New England Journal of Medicine. Libtayo has since been approved by the U.S. Food and Drug Administration (October 2025) and the European Commission (November 2025) as the first and only immunotherapy for this indication.
About the Phase 3 Trial
C-POST was a randomized, placebo-controlled, double-blind, multicenter, global Phase 3 trial investigating Libtayo versus placebo as adjuvant treatment for patients with features associated with a high-risk of CSCC recurrence and who had completed surgery and post-operative radiation therapy. Trial participants were at high risk of recurrence due to nodal features (extracapsular extension or ≥3 involved lymph nodes) and/or non-nodal features (in-transit metastases, T4 lesion, perineural invasion, or locally recurrent tumor with ≥1 additional poor prognostic features).
The trial enrolled 415 patients who were randomized to receive either Libtayo (n=209) or placebo (n=206) for up to 48 weeks. For the first 12 weeks, Libtayo 350 mg or placebo was administered intravenously every three weeks, followed by Libtayo 700 mg or placebo administered intravenously every six weeks for 36 weeks. After disease recurrence, patients randomized to placebo could cross over to receive Libtayo, and patients randomized to Libtayo could receive Libtayo again, if recurrence was ≥3 months since the last dose of adjuvant Libtayo.
About Regeneron in Cancer
We aspire to turn revolutionary discoveries into medicines that can transform the lives of those impacted by cancer. Our team around the world is driven to solve the needs and challenges of those affected by one of the most serious diseases of our time.
Backed by our legacy of scientific innovation and a deep understanding of biology, genetics and the immune system, we’re pursuing potential therapies across more than 30 types of solid tumors and blood cancers. Our cancer strategy is powered by cutting-edge technologies and therapies that can be flexibly combined to investigate potentially transformative treatments for patients. Oncology assets in clinical development comprise nearly half of Regeneron’s pipeline, and include checkpoint inhibitors, bispecific antibodies and costimulatory bispecific antibodies. Our approved PD-1 inhibitor Libtayo serves as the backbone of many of our investigational combinations.
To complement our extensive in-house capabilities, we collaborate with patients, healthcare providers, governments, biopharma companies and each other to further our shared goals. Together, we are united in the mission to serve as a beacon of transformation in cancer care.
About Libtayo
Libtayo is a fully human monoclonal antibody targeting the immune checkpoint receptor PD-1 on T cells and was invented using Regeneron's proprietary VelocImmune® technology. By binding to PD-1, Libtayo has been shown to block cancer cells from using the PD-1 pathway to suppress T-cell activation. Libtayo has been approved by regulatory authorities in more than 30 countries in one or more indications, including for certain adult patients with advanced basal cell carcinoma (BCC), CSCC that is advanced or at high risk of recurrence, advanced non-small cell lung cancer (NSCLC) and advanced cervical cancer.
In the U.S., the generic name for Libtayo in its approved indications is cemiplimab-rwlc, with rwlc as the suffix designated in accordance with Nonproprietary Naming of Biological Products Guidance for Industry issued by the U.S. FDA. Outside of the U.S., the generic name of Libtayo in its approved indications is cemiplimab.
The extensive clinical program for Libtayo is focused on difficult-to-treat cancers. Libtayo is currently being investigated in trials as a monotherapy, as well as in combination with either conventional or novel therapeutic approaches for other solid tumors. These potential uses are investigational, and their safety and efficacy have not been evaluated by any regulatory authority.
U.S. FDA-approved Indications
Libtayo is a prescription medicine used to treat:
Adults with a type of skin cancer called cutaneous squamous cell carcinoma (CSCC): that has spread or cannot be cured by surgery or radiation, orto help prevent CSCC from coming back if your CSCC is at high risk of coming back after it has been removed by surgery and radiation. Adults with a type of skin cancer called basal cell carcinoma (BCC) when your BCC cannot be removed by surgery (locally advanced BCC) or when it has spread (metastatic BCC) and have received treatment with a hedgehog pathway inhibitor (HHI), or cannot receive treatment with a HHI.Adults with a type of lung cancer called non-small cell lung cancer (NSCLC). LIBTAYO may be used in combination with chemotherapy that contains a platinum medicine as your first treatment when your lung cancer has not spread outside your chest (locally advanced lung cancer) and you cannot have surgery or chemotherapy with radiation, or your lung cancer has spread to other areas of your body (metastatic lung cancer), and your tumor does not have an abnormal “EGFR,” “ALK,” or “ROS1” gene.LIBTAYO may be used alone as your first treatment when your lung cancer has not spread outside your chest (locally advanced lung cancer) and you cannot have surgery or chemotherapy with radiation, or your lung cancer has spread to other areas of your body (metastatic lung cancer), and your tumor tests positive for high “PD-L1,” and your tumor does not have an abnormal “EGFR,” “ALK,” or “ROS1” gene.
It is not known if Libtayo is safe and effective in children.
IMPORTANT SAFETY INFORMATION FOR U.S. PATIENTS
What is the most important information I should know about LIBTAYO?
LIBTAYO is a medicine that may treat certain cancers by working with your immune system. LIBTAYO can cause your immune system to attack normal organs and tissues in any area of your body and can affect the way they work. These problems can sometimes become severe or life-threatening and can lead to death. You can have more than one of these problems at the same time. These problems may happen anytime during treatment or even after your treatment has ended.
Call or see your healthcare provider right away if you develop any new or worsening signs or symptoms, including:
Lung problems: cough, shortness of breath, or chest painIntestinal problems: diarrhea (loose stools) or more frequent bowel movements than usual, stools that are black, tarry, sticky or have blood or mucus, or severe stomach-area (abdomen) pain or tendernessLiver problems: yellowing of your skin or the whites of your eyes, severe nausea or vomiting, pain on the right side of your stomach-area (abdomen), dark urine (tea colored), or bleeding or bruising more easily than normalHormone gland problems: headache that will not go away or unusual headaches, eye sensitivity to light, eye problems, rapid heartbeat, increased sweating, extreme tiredness, weight gain or weight loss, feeling more hungry or thirsty than usual, urinating more often than usual, hair loss, feeling cold, constipation, your voice gets deeper, dizziness or fainting, or changes in mood or behavior, such as decreased sex drive, irritability, or forgetfulnessKidney problems: decrease in your amount of urine, blood in your urine, swelling of your ankles, or loss of appetiteSkin problems: rash, itching, skin blistering or peeling, painful sores or ulcers in mouth or nose, throat, or genital area, fever or flu-like symptoms, or swollen lymph nodesProblems can also happen in other organs and tissues. These are not all of the signs and symptoms of immune system problems that can happen with LIBTAYO. Call or see your healthcare provider right away for any new or worsening signs or symptoms, which may include: chest pain, irregular heartbeat, shortness of breath or swelling of ankles, confusion, sleepiness, memory problems, changes in mood or behavior, stiff neck, balance problems, tingling or numbness of the arms or legs, double vision, blurry vision, sensitivity to light, eye pain, changes in eyesight, persistent or severe muscle pain or weakness, muscle cramps, low red blood cells, or bruisingInfusion reactions that can sometimes be severe or life-threatening. Signs and symptoms of infusion reactions may include: nausea, vomiting, chills or shaking, itching or rash, flushing, shortness of breath or wheezing, dizziness, feel like passing out, fever, back or neck pain, or facial swellingRejection of a transplanted organ or tissue. Your healthcare provider should tell you what signs and symptoms you should report and monitor you, depending on the type of organ or tissue transplant that you have hadComplications, including graft-versus-host disease (GVHD), in people who have received a bone marrow (stem cell) transplant that uses donor stem cells (allogeneic). These complications can be serious and can lead to death. These complications may happen if you underwent transplantation either before or after being treated with LIBTAYO. Your healthcare provider will monitor you for these complications Getting medical treatment right away may help keep these problems from becoming more serious. Your healthcare provider will check you for these problems during your treatment with LIBTAYO. Your healthcare provider may treat you with corticosteroid or hormone replacement medicines. Your healthcare provider may also need to delay or completely stop treatment with LIBTAYO if you have severe side effects.
Before you receive LIBTAYO, tell your healthcare provider about all your medical conditions, including if you:
have immune system problems such as Crohn’s disease, ulcerative colitis, or lupushave received an organ or tissue transplant, including corneal transplanthave received or plan to receive a stem cell transplant that uses donor stem cells (allogeneic)have received radiation treatment to your chest areahave a condition that affects your nervous system, such as myasthenia gravis or Guillain-Barré syndromeare pregnant or plan to become pregnant. LIBTAYO can harm your unborn baby Females who are able to become pregnant:
Your healthcare provider will give you a pregnancy test before you start treatmentYou should use an effective method of birth control during your treatment and for at least 4 months after your last dose of LIBTAYO. Talk to your healthcare provider about birth control methods that you can use during this timeTell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with LIBTAYO are breastfeeding or plan to breastfeed. It is not known if LIBTAYO passes into your breast milk. Do not breastfeed during treatment and for at least 4 months after the last dose of LIBTAYO Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
The most common side effects of LIBTAYO when used alone to treat CSCC that has spread or cannot be cured by surgery or radiation, BCC or NSCLC include tiredness, muscle or bone pain, rash, diarrhea, and low levels of red blood cells (anemia).
The most common side effects of LIBTAYO when used alone to help prevent CSCC from coming back include rash and itching.
The most common side effects of LIBTAYO when used in combination with platinum-containing chemotherapy to treat NSCLC include hair loss, muscle or bone pain, nausea, tiredness, numbness, pain, tingling, or burning in your hands or feet, and decreased appetite.
These are not all the possible side effects of LIBTAYO. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to Regeneron Pharmaceuticals at 1-877-542-8296.
Please see full Prescribing Information, including Medication Guide.
About Regeneron's VelocImmune Technology
Regeneron's VelocImmune technology utilizes a proprietary genetically engineered mouse platform endowed with a genetically humanized immune system to produce optimized fully human antibodies. When Regeneron's Co-Founder, President and Chief Scientific Officer George D. Yancopoulos was a graduate student with his mentor Frederick W. Alt in 1985, they were the first to envision making such a genetically humanized mouse, and Regeneron has spent decades inventing and developing VelocImmune and related VelociSuite® technologies. Dr. Yancopoulos and his team have used VelocImmune technology to create a substantial proportion of all original, FDA-approved or authorized fully human monoclonal antibodies. This includes Dupixent® (dupilumab), Libtayo, Praluent® (alirocumab), Kevzara® (sarilumab), Evkeeza® (evinacumab-dgnb), Inmazeb® (atoltivimab, maftivimab and odesivimab-ebgn), Veopoz® (pozelimab-bbfg) and Pasatru™ (garetosmab-grts). In addition, REGEN-COV® (casirivimab and imdevimab) had been authorized by the FDA during the COVID-19 pandemic until 2024. A total of 11 antibody and bispecific products have been approved or authorized worldwide that were invented or derived using VelocImmune technologies.
About Regeneron
Regeneron (NASDAQ: REGN) is a leading biotechnology company that invents, develops and commercializes life-transforming medicines for people with serious diseases. Founded and led by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to numerous approved treatments and product candidates in development, most of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurological diseases, hematologic conditions, infectious diseases, and rare diseases.
Regeneron pushes the boundaries of scientific discovery and accelerates drug development using our proprietary technologies, such as VelociSuite®, which produces optimized fully human antibodies and new classes of bispecific antibodies. We are shaping the next frontier of medicine with data-powered insights from the Regeneron Genetics Center® and pioneering genetic medicine platforms, enabling us to identify innovative targets and complementary approaches to potentially treat or cure diseases.
For more information, please visit www.Regeneron.com or follow Regeneron on LinkedIn, Instagram, Facebook or X.
Forward-Looking Statements and Use of Digital Media
This press release includes forward-looking statements that involve risks and uncertainties relating to future events and the future performance of Regeneron Pharmaceuticals, Inc. (“Regeneron” or the “Company”), and actual events or results may differ materially from these forward-looking statements. Words such as “anticipate,” “expect,” “intend,” “plan,” “believe,” “seek,” “estimate,” variations of such words, and similar expressions are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. These statements concern, and these risks and uncertainties include, among others, the nature, timing, and possible success and therapeutic applications of products marketed or otherwise commercialized by Regeneron and/or its collaborators or licensees (collectively, “Regeneron’s Products”) and product candidates being developed by Regeneron and/or its collaborators or licensees (collectively, “Regeneron’s Product Candidates”) and research and clinical programs now underway or planned, including without limitation Libtayo® (cemiplimab) as adjuvant treatment for patients with cutaneous squamous cell carcinoma at a high risk of recurrence after surgery and radiation; uncertainty of the utilization, market acceptance, and/or commercial success of Regeneron’s Products (such as Libtayo) and Regeneron’s Product Candidates and the impact of studies (whether conducted by Regeneron or others and whether mandated or voluntary), including the studies discussed or referenced in this press release, on any of the foregoing; the likelihood, timing, and scope of possible regulatory approval and commercial launch of Regeneron’s Product Candidates and new indications for Regeneron’s Products; the ability of Regeneron’s collaborators, licensees, suppliers, or other third parties (as applicable) to perform manufacturing, filling, finishing, packaging, labeling, distribution, and other steps related to Regeneron’s Products and Regeneron’s Product Candidates; the ability of Regeneron to manage supply chains for multiple products and product candidates and risks associated with tariffs and other trade restrictions; safety issues resulting from the administration of Regeneron’s Products (such as Libtayo) and Regeneron’s Product Candidates in patients, including serious complications or side effects in connection with the use of Regeneron’s Products and Regeneron’s Product Candidates in clinical trials; determinations by regulatory and administrative governmental authorities which may delay or restrict Regeneron’s ability to continue to develop or commercialize Regeneron’s Products and Regeneron’s Product Candidates; ongoing regulatory obligations and oversight impacting Regeneron’s Products, research and clinical programs, and business, including those relating to patient privacy; the availability and extent of reimbursement or copay assistance for Regeneron’s Products from third-party payors and other third parties, including private payor healthcare and insurance programs, health maintenance organizations, pharmacy benefit management companies, and government programs such as Medicare and Medicaid; coverage and reimbursement determinations by such payors and other third parties and new policies and procedures adopted by such payors and other third parties; changes to drug pricing regulations and requirements and Regeneron’s pricing strategy, including in connection with Regeneron’s April 2026 agreements with the U.S. government; other changes in laws, regulations, and policies affecting the healthcare industry; competing products and product candidates (including biosimilar products) that may be superior to, or more cost effective than, Regeneron’s Products and Regeneron’s Product Candidates; the extent to which the results from the research and development programs conducted by Regeneron and/or its collaborators or licensees may be replicated in other studies and/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; unanticipated expenses; the costs of developing, producing, and selling products; the ability of Regeneron to meet any of its financial projections or guidance and changes to the assumptions underlying those projections or guidance; the potential for any license, collaboration, or supply agreement, including Regeneron’s agreements with Sanofi and Bayer (or their respective affiliated companies, as applicable), to be cancelled or terminated; the impact of public health outbreaks, epidemics, or pandemics on Regeneron's business; and risks associated with litigation and other proceedings and government investigations relating to the Company and/or its operations (including the pending civil proceedings initiated or joined by the U.S. Department of Justice and the U.S. Attorney's Office for the District of Massachusetts), risks associated with intellectual property of other parties and pending or future litigation relating thereto (including without limitation the patent litigation and other related proceedings relating to EYLEA® (aflibercept) Injection), the ultimate outcome of any such proceedings and investigations, and the impact any of the foregoing may have on Regeneron’s business, prospects, operating results, and financial condition. A more complete description of these and other material risks can be found in Regeneron’s filings with the U.S. Securities and Exchange Commission, including its Form 10-K for the year ended December 31, 2025 and its Form 10-Q for the quarterly period ended June 30, 2026. Any forward-looking statements are made based on management’s current beliefs and judgment, and the reader is cautioned not to rely on any forward-looking statements made by Regeneron. Regeneron does not undertake any obligation to update (publicly or otherwise) any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events, or otherwise.
Regeneron uses its media and investor relations website and social media outlets to publish important information about the Company, including information that may be deemed material to investors. Financial and other information about Regeneron is routinely posted and is accessible on Regeneron's media and investor relations website (https://investor.regeneron.com) and its LinkedIn page (https://www.linkedin.com/company/regeneron-pharmaceuticals).
BioNTech a Bristol Myers Squibb: pumitamig v kombinaci s docetaxelem dosáhl ve studii fáze 2 u pokročilého NSCLC míry objektivní léčebné odpovědi ve výši 36,7 % a mediánu PFS 6,9 měsíce.
Pumitamig plus docetaxel demonstrated encouraging responses in squamous and non-squamous non-small cell lung cancer across PD-L1 expression levels with a confirmed objective response rate of 36.7% following progression on or after immunotherapy plus chemotherapyAn early median progression-free survival of 6.9 months was observedSignificant unmet need remains for patients who have progressed on an immunotherapy-containing regimen, with the average progression-free survival below 4 months for standard of care docetaxel Data represent the third global Phase 2 dataset for pumitamig in lung cancer and reinforce its potential to improve outcomes over current standards of care MAINZ, Germany, and PRINCETON, USA, October 25, 2026 – BioNTech SE (Nasdaq: BNTX, “BioNTech”) and Bristol Myers Squibb Company (NYSE: BMY, “BMS”) today announced first data from the global Phase 2 ROSETTA Lung-107 clinical trial (NCT06841055) evaluating pumitamig, an investigational PD-L1xVEGF-A bispecific immunomodulator (BNT327/BMS986545), in combination with docetaxel in patients with metastatic non-small cell lung cancer (“NSCLC”) whose disease progressed on or after first-line immunotherapy plus chemotherapy.
The data showed encouraging antitumor activity, with responses observed in both squamous and non-squamous NSCLC and across PD-L1 expression levels, together with a manageable safety profile consistent with prior global datasets for pumitamig. The data were presented today in a late-breaking rapid oral presentation (abstract #LBA76) at the European Society for Medical Oncology (“ESMO”) Congress 2026 in Madrid, Spain.
“Despite meaningful advances in first-line treatment, outcomes remain poor for the many patients with non-small cell lung cancer whose disease progresses after immunotherapy plus chemotherapy, a setting where docetaxel has remained the standard of care for years,”1 said Byoung Chul Cho, M.D., Ph.D., Trial Investigator and Professor of Medical Oncology at Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea. “These first data from ROSETTA Lung-107 show encouraging response rates and progression-free survival across PD-L1 expression levels and histology, suggesting that pumitamig may help re-engage antitumor immunity in patients who have progressed on prior immunotherapy plus chemotherapy. These findings support continued investigation of pumitamig in this population with high unmet need.”
ROSETTA Lung-107 is evaluating pumitamig 1400 mg in combination with docetaxel every three weeks. The July 10, 2026, data cut-off included 50 patients with a median follow-up of 12.2 weeks, and 33 patients remained on treatment. Among 30 efficacy-evaluable patients, pumitamig plus docetaxel showed a confirmed objective response rate (“cORR”) of 36.7% with a disease control rate (“DCR”) of 90.0%. Responses were observed across PD-L1 expression levels (cORR: 42.9% TPS ˂ 1%; 33.3% TPS 1–49%; 40.0% TPS ≥ 50%) and histologies (cORR: 57.1% squamous; 30.4% non-squamous), with DCRs above 80% in all subgroups. Median time to response was 1.4 months. In the overall treated population (n=50), median progression-free survival (“PFS”) was 6.9 months (95% CI: 4.2 – not reached), with a six-month PFS rate of 63.3%. Historically, standard-of-care docetaxel has delivered a median PFS of approximately 3.6 or 3.9 months for non-squamous and squamous metastatic NSCLC patients, respectively, following prior immunotherapy plus chemotherapy.1
“Our ambition is to improve outcomes for patients across the full spectrum of lung cancer, spanning disease subtypes, stages and lines of therapy,” said Prof. Özlem Türeci, M.D., Co-Founder and Chief Medical Officer at BioNTech. “These encouraging results for pumitamig plus docetaxel extend the clinical evidence to patients whose disease has progressed after immunotherapy plus chemotherapy, a setting in which treatment options remain limited. Together with our findings in first-line NSCLC and extensive-stage small cell lung cancer, they support our strategy to develop pumitamig across a broad range of lung cancer settings, including those with particularly high unmet medical need.”
“This is the third global Phase 2 dataset to show consistent activity for pumitamig in lung cancer across PD-L1 expression levels, and it extends our evidence into a second-line setting where current options fall short,” said Cristian Massacesi, Executive Vice President, Chief Medical Officer and Head of Development at Bristol Myers Squibb. “Together with BioNTech, we are advancing one of the broadest development programs in the class as we continue to build the growing body of clinical evidence for pumitamig across multiple types and treatment lines of lung cancer, with four ongoing global Phase 3 trials, and we look forward to defining the path forward for pumitamig in second-line NSCLC.”
Across 50 patients in the safety evaluation, pumitamig plus chemotherapy showed a manageable safety profile, with no new safety signals. Pumitamig treatment-related adverse events (“TRAEs”) of any grade were reported in 52.0% of patients and grade ≥ 3 TRAEs in 18.0%, leading to treatment discontinuation in four (8.0%) patients. Immune- related AEs occurred in 11 (22.0%) patients and grade ≥ 3 immune- related AEs in five (10.0%) patients. VEGF-related events were reported in 13 (26.0%) patients; grade 3 events were rare (two patients, 4.0%), with no grade 4 or 5 events. Bleeding events occurred in eight (16.0%) patients and were limited to grade 1 or 2 severity. There were no pumitamig-related deaths or dose-limiting toxicities (“DLTs”).
BioNTech and BMS are advancing a broad development plan for pumitamig in multiple cancer types, including lung cancer across disease stages, subgroups and lines of therapy. ROSETTA Lung-107 extends the program into the second-line NSCLC setting, and these data will inform the further development of pumitamig in this underserved patient population.
About ROSETTA Lung-107
The global, open-label, single-arm Phase 2 ROSETTA Lung-107 trial (NCT06841055) is evaluating pumitamig (BNT327/BMS986545) in combination with docetaxel in patients with stage IV squamous or non-squamous NSCLC whose disease progressed following first-line immunotherapy plus chemotherapy, with any level of PD-L1 expression. Patients with prior exposure to anti-VEGF monoclonal antibodies or PD-(L)1xVEGF bispecific antibodies were excluded. In Part 1 (safety run-in), patients received pumitamig 1400 mg or 2000 mg plus docetaxel 75 mg/m² every three weeks (Q3W). In Part 2 (dose expansion), patients received pumitamig 1400 mg plus docetaxel 75 mg/m² Q3W, the dose recommended by the internal review committee based on the totality of evidence from Part 1 and the broader pumitamig lung cancer program. The primary endpoints are dose-limiting toxicities (Part 1 only), safety, and objective response rate (“ORR”) per investigator’s assessment (RECIST 1.1). Secondary endpoints include disease control rate (“DCR”), duration of response (“DOR”), depth of response, time to response, progression-free survival (“PFS”), overall survival (“OS”), pharmacokinetics, and antidrug antibody prevalence. The trial enrolled 59 patients at sites in Australia, the Republic of Korea, Spain, Türkiye, the United Kingdom, and the United States.
About Pumitamig
Pumitamig is an investigational bispecific immunomodulator, jointly developed by BioNTech and BMS, designed to cooperatively bind to PD-L1 and VEGF-A. It is aimed at restoring the immune system’s ability to recognize and destroy tumor cells while simultaneously cutting off the blood and oxygen supply that feeds tumor cells (anti-angiogenesis effect), preventing them from growing and proliferating. By anchoring to PD-L1 receptors on tumor cells, we believe pumitamig localizes VEGF-A blockade within the tumor microenvironment, potentially enhancing antitumor activity while minimizing systemic exposure.
More than 4,000 patients have been treated with pumitamig in clinical trials to date. Seven global Phase 3 trials with registrational potential are currently ongoing, evaluating pumitamig plus chemotherapy compared to standard of care treatments, in first-line small cell lung cancer (ROSETTA Lung-01, NCT06712355); first-line non-small cell lung cancer (ROSETTA Lung-02, NCT06712316); unresectable stage III non-small cell lung cancer (ROSETTA Lung-201, NCT07361497); first-line advanced PD-L1 ≥ 50% non-small cell lung cancer (ROSETTA Lung-202, NCT07361510); first-line triple-negative breast cancer (ROSETTA Breast-01, NCT07173751); first-line microsatellite stable colorectal cancer (ROSETTA CRC-203, NCT07221357); and first-line gastric cancer (ROSETTA Gastric-204, NCT07221149). Pumitamig is also being explored in 10+ novel-novel combination trials with ADCs and other novel modalities, with the aim of expanding its role across tumor types and identifying additional pivotal opportunities.
About NSCLC
Non-small cell lung cancer (NSCLC) covers all epithelial lung cancers other than small cell lung cancer and includes squamous cell carcinoma, large cell carcinoma, and adenocarcinoma of the lung. It is the most common type of lung cancer, accounting for approximately 85% of cases, and is the leading cause of cancer-related deaths worldwide.2 Scientific advances have transformed the treatment of NSCLC, improving outcomes for many patients. However, NSCLC remains an aggressive disease with a poor prognosis and a 5-year survival rate of 18 to 22% in advanced stages.3 Patients with low levels of PD-L1 expression typically do not respond well to checkpoint inhibitor-based regimens creating a significant unmet need for new treatment options that provide durable responses to a broad range of patients.
About BioNTech
BioNTech is a global next generation biopharmaceutical company pioneering novel investigative therapies for cancer and other serious diseases. In oncology, BioNTech is committed to transforming how cancer is treated. Its ambition is to develop innovative medicines with pan-tumor or synergistic potential to address cancer from multiple angles and across the full continuum of the disease from early- to late-stage. Its growing late-stage oncology pipeline comprises complementary treatment approaches spanning immunomodulators, antibody-drug conjugates, and mRNA cancer immunotherapies. BioNTech has partnered with multiple global and specialized pharmaceutical collaborators leveraging complementary expertise and resources to accelerate innovation and drive progress, including Bristol Myers Squibb, Duality Biologics, Genentech, a member of the Roche Group, Genmab, MediLink, OncoC4, and Pfizer.
For more information, please visit www.BioNTech.com.
BioNTech Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, but not limited to, statements concerning: BioNTech’s collaboration with Bristol Myers Squibb (BMS); BioNTech and BMS’s ability to successfully co-develop and co-commercialize pumitamig (also known as BNT327 or BMS986545), if approved; the rate and degree of market acceptance of pumitamig, if approved; the initiation, timing, progress, and results of BioNTech’s research and development programs, including BioNTech’s current and future clinical trials, including statements regarding the expected timing of initiation, enrollment, and completion of trials and related preparatory work and the availability of results, and the timing and outcome of applications for regulatory approvals and marketing authorizations, including expectations regarding the potential indications in which pumitamig may be approved, if at all; the targeted timing and number of additional potentially registrational trials, and the registrational potential of any trial BioNTech may initiate; and discussions with regulatory agencies. In some cases, forward-looking statements can be identified by terminology such as “will,” “may,” “should,” “expects,” “intends,” “plans,” “aims,” “anticipates,” “believes,” “estimates,” “predicts,” “potential,” “continue,” or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words.
The forward-looking statements in this press release are based on BioNTech’s current expectations and beliefs of future events and are neither promises nor guarantees. You should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond BioNTech’s control and which could cause actual results to differ materially and adversely from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to: the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as risks associated with clinical data, and including the possibility of unfavorable new preclinical, clinical or safety data and further analyses of existing preclinical, clinical or safety data; the nature of clinical data, which is subject to ongoing peer review, regulatory review and market interpretation; the impact of tariffs and escalations in trade policy; competition related to BioNTech’s product candidates; the timing of and BioNTech’s ability to obtain and maintain regulatory approval for its product candidates; BioNTech’s ability to identify research opportunities and discover and develop investigational medicines; the ability and willingness of BioNTech’s third-party collaborators to continue research and development activities relating to BioNTech’s product candidates and investigational medicines; unforeseen safety issues and potential claims that are alleged to arise from the use of products and product candidates developed or manufactured by BioNTech; BioNTech’s and its collaborators’ ability to commercialize and market its product candidates, if approved; BioNTech’s ability to manage its development and related expenses; regulatory and political developments in the United States and other countries; BioNTech’s ability to effectively scale its production capabilities and manufacture its products and product candidates; and other factors not known to BioNTech at this time.
You should review the risks and uncertainties described under the heading “Risk Factors” in BioNTech’s Report on Form 6-K for the period ended June 30, 2026 and in subsequent filings made by BioNTech with the SEC, which are available on the SEC’s website at www.sec.gov. These forward-looking statements speak only as of the date hereof. Except as required by law, BioNTech disclaims any intention or responsibility for updating or revising any forward-looking statements contained in this press release in the event of new information, future developments or otherwise.
About Bristol Myers Squibb
At Bristol Myers Squibb, our mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. We are pursuing bold science to define what’s possible for the future of medicine and the patients we serve. For more information, visit us at BMS.com and follow us on LinkedIn, X, YouTube, Facebook and Instagram.
Bristol Myers Squibb Cautionary Statement Regarding Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995 regarding, among other things, the research, development and commercialization of pharmaceutical products. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. Such forward-looking statements are based on current expectations and projections about Bristol Myers Squibb’s future financial results, goals, plans and objectives and involve inherent risks, assumptions and uncertainties, including internal or external factors that could delay, divert or change any of them in the next several years, that are difficult to predict, may be beyond our control and could cause future financial results, goals, plans and objectives to differ materially from those expressed in, or implied by, the statements. These risks, assumptions, uncertainties and other factors include, among others, that the expected benefits of, and opportunities related to the collaboration with BioNTech may not be realized by Bristol Myers Squibb or may take longer to realize than anticipated, that future study results may not be consistent with the results to date, that pumitamig (also known as BNT327 or BMS986545) alone or in combination with chemotherapy (such as docetaxel) may not achieve its primary study endpoint or receive regulatory approval for the indications described in this release in the currently anticipated timeline or at all, any marketing approvals, if granted, may have significant limitations on their use, and, if approved, whether pumitamig alone or in combination with chemotherapy will be commercially successful. No forward-looking statement can be guaranteed. Forward-looking statements in this press release should be evaluated together with the many risks and uncertainties that affect Bristol Myers Squibb’s business and market, particularly those identified in the cautionary statement and risk factors discussion in Bristol Myers Squibb’s Annual Report on Form 10-K for the year ended December 31, 2025, as updated by Bristol Myers Squibb’s subsequent Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and other filings with the Securities and Exchange Commission. The forward-looking statements included in this document are made only as of the date of this document and except as otherwise required by applicable law, Bristol Myers Squibb undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, changed circumstances or otherwise.
1. Ahn MJ et al. J Clin Oncol. 2025;43(3):260–272.
2. Lin Z et al. Medicine (Baltimore). 2025 Jul 25;104(30):e43300.
3. Liu SV et al. Immunotherapy. 2025 Oct;17(14):1005-1013.
Nuclear energy stocks have been in the doldrums this year. The Global X Uranium ETF (URA +0.06%) is down around 15% so far this year, reflecting the sector's overall malaise.
The reason for the decline is that the sector became a little overheated due to enthusiasm for nuclear energy, with technology companies signing deals to secure nuclear electricity for artificial intelligence (AI) data centers. While this points to long-term growth, many newer nuclear energy companies face a long road to profitability.
Instead of focusing on nuclear companies that may eventually turn things around, it makes more sense to look at pick-and-shovel nuclear stocks that are already profitable and benefiting from the growth of nuclear energy. One of those stocks is Centrus Energy (LEU -1.63%), the lone publicly traded proven U.S. uranium enricher. While shares of Centrus have plummeted more than 52% so far this year, the company remains a solid buy, and the stock's valuation has become more reasonable, trading at about 33 times forward earnings.
Here are three reasons to consider Centrus Energy.
Image source: Getty Images.
It has a first-mover advantage Centrus operates the only U.S. Nuclear Regulatory Commission (NRC)-licensed facility capable of producing high-assay low-enriched uranium (HALEU), the specialized fuel enriched between 5% and 20% U-235 required for almost all next-generation advanced small modular reactors (SMRs) and microreactors. The company finalized its $900 million order to produce HALEU for the U.S. Department of Energy (DOE) in July.
LEU Centrus Energy$102.45-$1.70 (-1.63%)
NYSE · As of 4:00 PM ET 10/23/26
With more companies racing to advance nuclear technologies, Centrus already has multi-year supply agreements with emerging reactor developers, such as X-energy, Radiant Industries, and Antares Nuclear. These partnerships, often backed by customer prepayments, make Centrus a central pick-and-shovel provider for the future nuclear tech boom.
It is showing dependable revenue growth In the second quarter, Centrus reported revenue of $176.1 million, up 13.9%, year over year. It is estimating full-year revenue between $450 million and $500 million, compared to $448.7 million in 2025.
Centrus has a $4.5 billion backlog, with work scheduled out to 2040. This shows that customers are locking in long-term orders for years to come. Of that total, $3.7 billion comes strictly from its primary fuel business of selling standard reactor fuel and uranium to power utilities.
These are mostly fixed, multi-year contracts for guaranteed future deliveries. In addition to its fixed orders, it has agreed to $3 billion in potential future sales of low-enriched uranium (LEU) and HALEU.
Adjusted net income was $38.7 million, up 12% over the same period a year ago, but adjusted earnings per share (EPS) were $1.95, flat compared to the second quarter of 2025.
It has a huge moat The United States hasn't had its own active facility to enrich uranium for national security and defense needs since the Paducah, Kentucky, plant closed in 2013. The DOE is relying on Cold War-era stockpiles. Because this supply is finite and shrinking, the U.S. will soon need a new domestic source of enriched uranium to replace it.
Due to long-standing government policies and international nonproliferation agreements, the U.S. military and national security agencies are forbidden from using foreign enrichment technology or foreign-sourced fuel for national defense purposes.
Centrus's proprietary technology, its AC100M centrifuge, is the only American-developed, deployment-ready uranium enrichment system available that complies with U.S. legal and national security requirements.
The company's first-mover advantage in uranium enrichment and growing backlog make the stock a solid buy. It is already growing revenue and is profitable, giving it a big advantage over other AI stocks. The stock's tumble appears related more to sector concerns than its financial health, which appears sound.
Akcie Altria do 12. října posílily o 28 % oproti 13% růstu indexu S&P 500; dividendový výnos činí 5,8 % a společnost dividendu zvyšuje již 57 let v řadě.
Plenty of stocks pay dividends, but not all of those qualify as true dividend stocks. Tobacco giant Altria (MO -2.31%) does.
Altria is a poster child for dividend stocks, routinely boasting one of the highest yields in the S&P 500 (^GSPC -0.52%). This year, though, the stock has displayed more of the characteristics of a growth stock than a typical income stock. Through the market close on Oct. 12, Altria was up by 28% compared to the S&P 500's 13%.
After that impressive run-up so far in 2026, is the stock still a good buy?
Image source: The Motley Fool.
A premier dividend stock
Despite its unusual price gains, the appeal of Altria's stock is undoubtedly based on its dividend. The company is well aware that those quarterly payouts are why some investors flock to the stock, so it prioritizes maintaining and increasing them.
At the current share price, Altria's yield is 5.8%, which is more than 5.5 times what you'd get from an S&P 500 ETF today, but still less than its average over the past five years.
MO Dividend Yield data by YCharts.
High yield aside, Altria's dividend has been the definition of consistency. The company is a Dividend King (a company with at least 50 consecutive years of dividend increases). Its streak now stands at 57 straight years. Of the thousands of stocks trading on the U.S. market, only 25 have longer dividend-hiking streaks.
MO Altria Group$74.31-$1.76 (-2.31%)
NYSE · As of 4:00 PM ET 10/23/26
Using pricing power to keep the train rolling
Altria has been the country's leading tobacco company for quite some time, leaning on its iconic brands like Marlboro, Copenhagen, Black & Mild, and others.
The nature of its business has been a double-edged sword over the past decade or so. On one hand, people are smoking cigarettes much less. A recently published report shows the smoking rate among U.S. adults at 9.9%, the lowest percentage ever recorded. This inevitably affects the country's largest cigarette producer.
On the other hand, the tobacco industry comes with lots of pricing power because many smokers are brand loyal and buy their preferred brand regardless of price. So, while Altria's cigarette sales volumes have been falling, it has offset some of those declines by steadily raising prices.
Investors don't expect huge revenue growth from Altria, so flat or occasional declines aren't deal-breakers. As long as its business is healthy enough to keep the dividends coming, many investors are perfectly content.
MO Revenue (Quarterly YoY Growth) data by YCharts.
Altria is generally more concerned with its earnings per share (EPS), because earnings are what fund its dividends and its stock buybacks. In the second quarter, its adjusted EPS grew 2.8% year over year, down from 7.3% growth in the first quarter. For a company of its size and maturity, though, that's solid.
Is Altria a buy?
Some people point to the declining smoking rates as the central hindrance to Altria's long-term success. That's a real problem for the company, no doubt, but I don't think it's as imminent a threat to its business as some may believe. It's true that "just keep raising prices" isn't a great long-term business model, but it does buy Altria time to become a true player in the smokeless nicotine space.
Altria's on! nicotine pouches have been getting good distribution, but they still don't compare to the popularity and success of Philip Morris International's Zyn nicotine pouches. Regardless, any progress is better than none, and after Altria's previous swings and misses in the space, investors should be glad for now.
If you're looking for a solid dividend stock, Altria is a great option. As mentioned, the company isn't oblivious to the fact that most shareholders only stick around for the dividend. If it lets the appeal of that dividend fade, it loses investors, which would present a bigger problem for management.
There are plenty of things Altria would do operationally before putting its dividend on the chopping block. That doesn't make the stock a foolproof investment, but if you're looking for a good income source, Altria provides that. I don't see that changing anytime in the foreseeable future.
Vicor ve 3. čtvrtletí zvýšil tržby meziročně o 78,5 % na 197,1 mil. USD a hrubou marži na 68,3 %; do 2. čtvrtletí 2027 chce kapacitu zvýšit zhruba na pětinásobek.
SummaryI reiterate my Strong Buy on Vicor after a record Q3, despite a 38% drawdown since my last article driven by sector-wide AI hardware selling.Q3 revenue rose 78.5% YoY to $197.1M, with product revenue up 47%, royalties up 207%, and gross margin reaching 68.3%.Vicor is supply-constrained rather than demand-constrained, with Fab 1 nearly full and two new fab sites targeting about 5x capacity from Q2 2027.Management expects to fund the expansion entirely from cash, in contrast with peers financing AI buildouts through debt or large equity raises.My FY27 scenarios range from -36% to +103%, with a base case of +44%. Thomas Barwick/DigitalVision via Getty Images
Investment Thesis Despite the volatility in the share price and negative returns over the last few months, I reiterate my Strong Buy rating on Vicor (VICR) based on fundamental improvements across many
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Analyst’s Disclosure: I/we have a beneficial long position in the shares of VICR either through stock ownership, options, or other derivatives. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.
Seeking Alpha's Disclosure: Past performance is no guarantee of future results. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. Any views or opinions expressed above may not reflect those of Seeking Alpha as a whole. Seeking Alpha is not a licensed securities dealer, broker or US investment adviser or investment bank. Our analysts are third party authors that include both professional investors and individual investors who may not be licensed or certified by any institute or regulatory body.
FitLife Brands čelí slabšímu organickému růstu v důsledku změn na Amazonu a nižší poptávky, přesto se její čtvrtletní tržby držely kolem 25–26 milionů USD.
FitLife Brands NASDAQ: FTLF outlined its strategy to grow a portfolio of nutritional supplement and wellness brands through acquisitions, e-commerce sales and operational improvements, while acknowledging recent organic-growth headwinds tied to Amazon changes, specialty retail traffic and weakening demand in certain product categories.
Chairman and Chief Executive Officer Dayton Judd said FitLife owns 16 brands and operates as an asset-light business, owning brand intellectual property while using third parties for manufacturing. The company sells products through e-commerce and wholesale channels, including GNC franchise stores, Walmart, CVS, Walgreens, Costco Canada, Sprouts, Fresh Thyme and Whole Foods.
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About half of FitLife's revenue comes from online sales, Judd said. The company does not sell products directly to Amazon, but instead operates as the seller of its brands on the marketplace and manages its own product pages and advertising.
Growth Strategy Built on Acquisitions
Judd described FitLife's transformation since he became interim CEO in 2018, when the company was facing debt default and was “literally on the verge of bankruptcy.” He said the company had been heavily dependent on GNC, with about 99% of revenue coming from wholesale sales before FitLife expanded its online operations, particularly on Amazon.
FitLife subsequently used cash flow from its existing businesses to acquire additional brands, seeking both growth and a more diversified customer base. Its recent transactions included Nutrology in April 2021, Mimi's Rock Corp., which included the Dr. Tobias brand, in February 2023, MusclePharm assets out of bankruptcy in October 2023, and Irwin Naturals more than a year ago.
Judd said the Irwin Naturals purchase roughly doubled FitLife's size. On a last-12-month basis, he said FitLife had more than $100 million in revenue and adjusted EBITDA of more than $14 million.
The company uses debt for acquisitions and seeks to pay it down afterward rather than issuing stock, according to Judd. He said FitLife has not issued shares for acquisitions and has a simple common-stock capital structure. Judd also said he owns about 60% of the company on a fully diluted basis, which he characterized as aligning management with shareholders.
Margin Improvement Efforts
President Ryan Hansen said the Irwin Naturals acquisition lowered FitLife's blended gross-margin profile because Irwin historically operated with somewhat lower margins. He said the combined company is currently generating gross margins in the mid-30% to high-30% range, compared with low-40% margins before the acquisition.
Management is working to improve those margins by extending shelf life across Irwin products where possible. Hansen said most Irwin products historically had two-year shelf lives, while retailers often require products to have at least 12 months of dating remaining before putting them on shelves.
That requirement effectively left the company with about a year to sell products after manufacturing, he said. Irwin had been recording more than $1 million and potentially close to $2 million annually in inventory obsolescence. FitLife has worked to transition formulas it owns to three-year shelf lives, which would double the sellable period from 12 months to 24 months.
Hansen said the benefit will take time to materialize because the company must first cycle through older inventory. FitLife also has made changes to its third-party logistics, transportation and distribution arrangements that are expected to reduce fulfillment costs. In addition, management has made SG&A and headcount adjustments following the Irwin acquisition.
Organic Challenges and Portfolio Response
Hansen said FitLife operates in a fragmented supplement market with favorable long-term category trends, but said growth has not been evenly distributed among competitors. The company identified three recent challenges to organic sales:
Amazon algorithm changes that have favored brands with traffic and presence outside the Amazon ecosystem.
Lower foot traffic at specialty retailers, where consumers may be more sensitive to premium prices.
Exposure to declining segments, including weight-loss and cleanse products affected by GLP-1 drugs, as well as certain men's health and testosterone-focused products.
Hansen said FitLife is responding by building external traffic through TikTok, Google and Meta advertising, while also pursuing generative-engine optimization to improve discovery through artificial-intelligence search tools. He said Irwin, which was already broadly distributed outside Amazon, has performed above the company's expectations since its acquisition.
Management also plans to introduce products outside the categories facing pressure. Hansen said the company's product-development pipeline is focused on areas where FitLife believes it has “permission to win” or an existing presence that can be expanded.
Judd emphasized that the company is not experiencing a rapid revenue decline. He said quarterly revenue over the prior three quarters had generally been in the $25 million to $26 million range, with declining brands and channels being substantially or fully offset by growth elsewhere. Still, he said FitLife needs to restore organic growth to support a higher valuation multiple.
Acquisition Market Remains Difficult
While FitLife intends to remain a consolidator in the supplement industry, Judd said the company has not found a transaction it feels compelled to pursue recently. He said FitLife has signed more than 75 nondisclosure agreements, and possibly close to 100, over roughly five years but has completed four deals.
Over the past year, Judd said the company reviewed about two dozen potential transactions and did not see a single business presented as growing. Many potential targets were direct-to-consumer businesses experiencing declines while spending heavily on advertising in an effort to stabilize sales, he said.
About FitLife Brands (NASDAQ:FTLF)FitLife Brands, Inc is a developer, manufacturer and marketer of nutritional supplements. The company focuses on products intended to support sports performance, weight management, energy, recovery and general health, serving consumers through a portfolio of branded dietary supplements.
FitLife's product portfolio has included brands such as NDS Nutrition, PMD Sports, iSatori and Muscle Elements. Its offerings include powders, capsules, tablets and other supplement formats marketed to athletes, fitness enthusiasts and consumers seeking wellness and nutrition products.
The company sells its products through e-commerce channels, specialty retailers, gyms and other distributors.
This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].
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Arrow Exploration zvýšila díky novým vrtům IC-8 a IC-7 v kolumbijském poli Icaco produkci na rekordních více než 6 500 barelů ropného ekvivalentu denně.
Arrow Exploration Corp (TSX-V:AXL, AIM:AXL, OTC:CSTPF) has pushed production to a record high of more than 6,500 barrels of oil equivalent per day (boe/d), following successful drilling at its Icaco field in Colombia.
The milestone comes as two new wells, IC-8 and IC-7, contribute a combined 1,452 barrels of oil per day (bopd) gross, equivalent to 726 bopd net to Arrow, at restricted production rates.
IC-8, which began producing on 12 October, is delivering approximately 1,204 bopd gross from the Carbonera C7 formation, while IC-7 is producing 248 bopd gross from the Ubaque formation. Both wells are located on the Tapir Block, where Arrow holds a 50% beneficial interest.
Chief executive Marshall Abbott said the multi-zone quality of the Icaco discovery and its production rates had "surpassed initial expectations".
Arrow also reported progress at its IC-HZ9 well, the first horizontal well targeting the Carbonera reservoir on the Tapir Block. Drilling was completed on 20 October, with the company identifying what appears to be 950 feet of horizontal oil pay.
The company estimated its cash balance at more than US$28 million as of 1 October and said it continues to pursue an extension of the Tapir Block through discussions with Colombian regulators.
Arrow has built 16 well cellars at Icaco and plans to continue drilling across the Carbonera C7, Gacheta and Ubaque formations.
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ADS společnosti Yiren Digital klesly 12. října 2026 o 44 % poté, co firma uvedla, že její generální ředitel Ning Tang byl v souvislosti s vyšetřováním některých přidružených společností ovládajícího akcionáře podroben trestním donucovacím opatřením.
Rosen Law Firm Encourages Yiren Digital Ltd. Investors to Inquire About Securities Class Action Investigation - YRDPR Newswire
NEW YORK, Oct. 24, 2026
, /PRNewswire/ --
Why: Rosen Law Firm, a global investor rights law firm, continues to investigate potential securities claims on behalf of shareholders of Yiren Digital Ltd. (NYSE: YRD) resulting from allegations that Yiren may have issued materially misleading business information to the investing public.
So What: If you purchased Yiren 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/cases/yiren-digital-ltd/join 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 October 12, 2026, Yiren issued a press release entitled "Yiren Digital Provides Update on Its CEO and Operations." The press release stated that Yiren had "became aware of a police notice published on October 12, 2026, stating that Mr. Ning Tang, the Company's Executive Chairman and Chief Executive Officer, had been subject to criminal compulsory measures in connection with an investigation involving certain affiliates of the Company's controlling shareholder."
On this news, Yiren's American Depositary Shares fell 44% on October 12, 2026.
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 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 billions 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.
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There was plenty to like about Lockheed Martin's (LMT +2.42%) earnings report on Oct. 22. The aerospace and defense manufacturer raised its full-year guidance for the second quarter in a row while beating Wall Street's third-quarter estimates. While the stock has risen more than 20% year to date as of this writing, Lockheed remains a solid buy for long-term investors.
$604.18+$14.27 (+2.42%)
NYSE · As of 4:00 PM ET 10/23/26
First and foremost, Lockheed's third-quarter sales grew 11% to $20.7 billion. Earnings per share beat analysts' expectations by nearly $0.50 at $7.97. All four of Lockheed's segments grew, with the Missiles and Fire Control business having the greatest gain, increasing 14% from this quarter last year.
Lockheed's management now expects sales to top $80 billion and free cash flow of $7.8 billion to $8 billion in 2026. The free cash flow number increased by $800 million from last quarter. Lockheed also increased its dividend again, marking 24 consecutive years of increases.
Image source: Getty Images.
The stock is really a buy because of the growth in backlog, which provides substantial revenue visibility. The backlog grew 27% to $292 billion this quarter. In particular, Lockheed signed multiyear deals for a PAC-3 interceptor and 850 F-35 jets.
Of course, Lockheed's success depends on its ability to execute efficiently and effectively, but for buy-and-hold investors, the backlog, rising guidance, and consistently growing dividend are excellent reasons to purchase the stock. Shares are still trading at a reasonable price. The company's forward and trailing price-to-earnings ratios are in the teens, and the dividend yield is respectable, currently around 2.5%.
Catie Hogan has no position in any of the stocks mentioned. The Motley Fool has positions in and recommends Lockheed Martin. The Motley Fool has a disclosure policy.
In case you hadn't heard, Rocket Lab (RKLB +2.69%) had some horrible news to tell investors last week (except it's not really so horrible). Once again, the company has decided to postpone the inaugural launch of its new Neutron reusable rocket.
What's more, Rocket Lab is being pretty vague about exactly when it hopes to launch.
Image source: Rocket Lab.
Rocket Lab's terrible, horrible, no good, very bad day
Rocket Lab broke the bad news about Neutron in an after-hours webcast on Oct. 14. The company had been hoping to get its first Neutron rocket off the ground before the end of 2026. But a problem arose during the manufacturing of the carbon composite "domes" assembled to form the tops and bottoms of its first-stage propellant tanks.
In essence, Rocket Lab discovered air pockets forming between the carbon composite layers that are laid down to form the domes. The air pockets weaken the structural integrity of the domes. They wouldn't necessarily cause the domes to fail and the rocket to explode in flight, but Rocket Lab didn't want to take chances and decided to delay the first flight until it could come up with a new manufacturing process to prevent air bubbles from forming.
You might think investors would approve of this approach, designed to make sure Rocket Lab's first Neutron flight did not end in disaster. But in fact, investors sold off Rocket Lab stock on the news, and the shares closed last week down 25%.
Now, the good news is that Rocket Lab thinks it's figured out a fix. "We've solved the problem," announced CEO Sir Peter Beck. The bad news, though -- or more precisely, the worse news -- is that the new delay into 2027 might be even longer than it sounds.
Management said it's now targeting a Neutron launch in 2027, but didn't specify when. Worse, Beck acknowledged that the 2027 target itself is "an ambitious timeline," which appears to imply that 2027 is itself a deadline that Rocket Lab may fail to meet.
RKLB Rocket Lab$52.60+$1.38 (+2.69%)
NASDAQ · As of 4:00 PM ET 10/23/26
What it means for Rocket Lab investors
So precisely how worried should Rocket Lab investors be about all of this?
Honestly, I think "worried" might be the wrong reaction here. If you own Rocket Lab stock, it's probably too much to hope you'd be happy about the news of yet another launch delay. But I suspect the correct attitude is more one of impatience to see that first flight, rather than worry about what a delay might mean for Rocket Lab stock.
Even if everything had gone right with Neutron's development, Rocket Lab was only anticipating one launch this year, followed by three next year, and five the year after that.
Simply put, the plan was always to roll out this rocket slowly, step by step, and increase its launch cadence over time. Given that it would take years for Neutron to move the needle on Rocket Lab's revenues anyway, the fact that management is taking a few extra months -- or even as long as a year -- to ensure everything goes smoothly won't affect Rocket Lab's revenues or profits much in the near term.
And longer term? As Beck explained, Rocket Lab is "building the program's long-term infrastructure at the same time as we build our first rocket, so that we can scale quickly" once all the kinks are worked out. "We won't rush to the pad with unnecessary risk," he said.
Frustrating as the delay may be, this sounds like the right approach to me. Plus, as I've explained before, it won't change the fact that Rocket Lab will almost certainly earn its first profit next year, with or without a Neutron launch.
"Long" story short, both near-term and long-term, I think Rocket Lab's going to do just fine.
FDA odložila rozhodnutí o zanzalintinibu na 3. března 2027 kvůli žádosti o dodatečné údaje. Vítězství v patentovém sporu chrání Cabometyx před generickou konkurencí v USA nejméně do ledna 2030.
Exelixis (EXEL -1.19%) has crushed the broader market this year, with its shares climbing 49%. However, the drugmaker recently hit a roadblock. The U.S. Food and Drug Administration (FDA) decided to extend the review period for Exelixis' zanzalintinib, an investigational medicine for colorectal cancer. The health regulatory agency requested more data before it can decide whether to approve the drug. A decision is now expected by March 3, 2027, pushed back from the original deadline of Dec. 3, 2026. That's not great news for Exelixis, but despite this setback, the company's prospects look attractive. Here are three reasons why.
Image source: The Motley Fool.
1. Winning the Cabometyx patent battle Exelixis' most important driver of revenue and earnings growth is Cabometyx, a medicine approved for various cancers, including liver and kidney cancers. Cabometyx is a tyrosine kinase inhibitor -- tyrosine kinase is a protein that plays a role in cell growth and division, a mechanism that is sometimes hijacked by cancer cells to promote rapid growth. Cabometyx has been one of the top-prescribed medicines of its kind in renal cell carcinoma (RCC, the most common form of kidney cancer) for years.
It has also continued to grind out new indications, including as a combination therapy. Exelixis' financial results have been strong thanks to this drug. In the second quarter, the company's revenue increased by 10.6% year over year to $628.7 million. Exelixis' earnings per share grew by about 26% year over year to $0.82.
Exelixis has done its best to delay the entry of cheaper Cabometyx generics in the U.S., and so far, it has been successful. Thanks to a patent lawsuit it won, it should not face generic competition in the U.S. at least until January 2030, perhaps even later if the company wins another patent case that starts in November. That should give Exelixis enough time to develop newer medicines to replace its crown jewel.
EXEL Exelixis$64.53-$0.78 (-1.19%)
NASDAQ · As of 4:00 PM ET 10/23/26
2. Zanzalintinib could be a pipeline-in-a-drug The most promising drug Exelixis is developing is zanzalintinib, and that's despite the recent regulatory setback. Consider the medicine's potential in colorectal cancer. It is the second leading cause of cancer death worldwide, which implies that there is a large opportunity in the market, particularly for the indication Exelixis is targeting: once it has metastasized. Further, Exelixis won't stop at this indication.
The biotech company will seek to follow the same blueprint it used for Cabometyx. Exelixis is testing zanzalintinib across several other forms of cancer. The list includes RCC, some kinds of lung cancer, and more. Of course, zanzalintinib won't earn every indication it targets. Cabometyx didn't either. But even a handful or so could make the medicine a massive commercial success and help usher in the next phase of growth for Exelixis.
Some analysts have estimated that zanzalintinib could generate $4.5 billion in U.S. sales by 2033 across various indications. Note that last year, the company made $2.3 billion in revenue, mostly from Cabometyx. Provided the sales estimates for zanzalintinib are accurate, this drug could eventually more than offset the loss of Cabometyx.
3. Exelixis' deep pipeline Even if zanzalintinib alone isn't enough to replace Cabometyx once the latter starts facing generic competition, Exelixis has a plan. The company boasts several other pipeline candidates that could eventually contribute. Although these are mostly still in early stage studies, they could make significant progress over the next five years. Most early stage candidates never make it to the market, but there is a decent chance that at least a couple of Exelixis' brand-new therapies will.
And even if none does, the company has research collaborations in place that could supply additional, oncology-focused drug candidates to its pipeline. Exelixis' ability to carve out a niche in the ruthlessly competitive oncology market, which is typically dominated by pharmaceutical giants, is fairly impressive. And over the medium term, the company could, once again, launch one or two brand-new cancer drugs that will help it sustain strong financial results and deliver competitive stock market returns.
Shares of UPS (UPS -0.45%) reached their all-time closing high of $232.11 on Feb. 2, 2022. As I write this, the stock trades around $100, about 57% off its peak and close to where it began 2026.
The fall has sent the dividend yield up to about 6.5%, based on the company's $1.64 quarterly payout. For a company so well known, a yield that size stands out, and it puts a lot of weight on what UPS reports next.
The parcel giant posts its third-quarter results before the market opens on Tuesday, Oct. 27. It'll be the first full quarter after UPS finished cutting the volume it handles for its biggest customer, Amazon.
Image source: The Motley Fool.
Earnings did most of the fallingA 57% slide might look like a market overreaction. But most of this one reflects a sharp fall in profits. In 2022, UPS earned $12.94 per share on a non-GAAP (adjusted) basis. For 2026, management expects around $7.22 -- a decline of about 44%.
Some of that drop was by design. In January 2025, UPS said it had reached an agreement in principle with its biggest customer to cut that customer's volume by over 50% by the second half of 2026. Management said in late August that the Amazon cutback, and the network revamp built around it, finished in June.
Sure, the stock fell hard. But so did the earnings underneath it, and that's why I don't think the size of the drop alone makes UPS a bargain. Has that slide finally bottomed?
A leaner networkThe early signs are promising. Showing what the cut was meant to achieve, UPS's second-quarter U.S. domestic revenue grew 6% year over year even as average daily volume slid 3.3%. Revenue per piece jumped 9.3%. The segment's adjusted operating margin widened to 8% from 7% in the year-ago quarter, and from just 4% in the first quarter of 2026. Also, its adjusted operating profit rose 21% year over year to around $1.2 billion.
Cost cutting is doing a lot of the work. UPS said its network and efficiency programs produced around $1.2 billion in benefits from January to June, and it expects about $3 billion for all of 2026. That leaves around $1.8 billion yet to come in the last six months -- more than the first half delivered.
The third quarter probably won't look as strong as the second, though. Management guided for about flat U.S. domestic revenue and an adjusted operating margin of around 7% for the segment in the third quarter.
But reaching that target means beating the 6.4% margin UPS reported in the same quarter last year. And management expects the segment's margin to average around 8.8% over the second half.
The second half has to deliverTuesday's report is the first test of that second-half forecast. First-half adjusted earnings per share were $2.82, so meeting the full-year target requires about $4.40 from July to December.
That looks like modest growth over the $4.12 UPS made in the back half of 2025. But last year's third-quarter result of $1.74 included a $0.30 bump from a gain on a sale-leaseback of five properties. Take that out, and second-half earnings per share have to climb around 15% year over year.
In other words, a third-quarter number below last year's $1.74 wouldn't necessarily mean the plan is slipping.
UPS United Parcel Service$101.06-$0.46 (-0.45%)
NYSE · As of 4:00 PM ET 10/23/26
Cash flow arguably counts even more for a stock yielding 6.5%. Management expects around $5.5 billion of free cash flow for 2026, including employee separation payments linked to its Driver Choice Program, against about $5.4 billion in dividend payments.
UPS produced around $1.6 billion in free cash flow through June. So it needs around $3.9 billion over the rest of the year to meet the target. That would cover the remaining $2.7 billion or so in dividends, but not by much.
Meanwhile, the stock's valuation looks fair. Shares trade at around 13 times earnings expected for 2027, a large discount to the S&P 500 (^GSPC -0.52%), which trades at about 19 times forward earnings.
So, is UPS stock a buy before Tuesday? I think it's worth a look at this price, especially for income investors willing to wait for the turnaround to show up in cash flow. The company has shed its least profitable volume, and the margins for its largest segment are going in the right direction.
Of course, one quarter could easily disappoint, and the dividend leaves little slack if second-half cash flow comes up short. But at that valuation, the stock price already seems to reflect a good deal of that risk.
Palantir Technologies (PLTR +0.28%) stock has been on an incredible run. While the stock's gain of roughly 13.5% is roughly in line with the rally for the S&P 500 (^GSPC -0.52%), the artificial intelligence (AI) software specialist has absolutely crushed the market on a longer timeline.
Over the last five years, Palantir stock has risen roughly 714%. Meanwhile, the S&P 500's level has climbed 70.5%. With Palantir now trading at roughly $200 per share, is it likely that the company is gearing up for a stock split in the near future?
Image source: Getty Images.
Don't count on a stock split just yet
In recent years, stock splits have become highly anticipated, closely watched market events -- and for good reason. The announcements and implementations of splits have coincided with substantial valuation gains for many companies that have implemented them.
A stock split doesn't alter a business's fundamentals. It simply cuts the pie that is a company's share count into a larger number of pieces.
As a result, the stock price is reduced by a corresponding ratio. While this doesn't improve the underlying business, the lower share price has often made shares more attractive to retail investors. In turn, increased buying action pushes the stock higher. Palantir has yet to conduct a stock split across its roughly six-year history as a publicly traded company.
PLTR Palantir Technologies$196.75+$0.56 (+0.28%)
NASDAQ · As of 4:00 PM ET 10/23/26
While I think there's a good chance additional share price gains will prompt the company to split within the next few years, I don't think there's anything to suggest a split is imminent. Trading at roughly $200 per share, Palantir stock isn't yet at a pure-dollar pricing level that's likely to spur a split.
If the stock approaches $500 per share and continues to show strength at that level, I think a split becomes much more likely. That's a level that is historically more likely to encourage stock splits.
So for investors hoping that a near-term stock split will help push Palantir stock higher, I don't think that's a solid bet. The good news is that Palantir doesn't have to rely on a stock split to boost its valuation.
In its second-quarter report published in August, Palantir announced that sales grew 93% year over year to $1.935 billion. Meanwhile, non-GAAP (generally accepted accounting principles) adjusted operating income came in at $1.194 billion -- good for a 62% margin.
Palantir is growing sales at an incredible pace and posting margins that are extremely impressive, even by the standards of high-margin software companies. These characteristics could continue to support bullish momentum for the stock.
CTX310 společnosti CRISPR Therapeutics ve studii fáze 1a při nejvyšší dávce snížil hladinu triglyceridů v průměru o 48 % a hladinu LDL cholesterolu o 53 %.
CRISPR Therapeutics (CRSP -1.20%) has a major claim to fame. It developed a medicine called Casgevy, which in 2023 became the first approved therapy to use the Nobel Prize-winning CRISPR gene-editing technique. Casgevy is currently CRISPR Therapeutics' only approved medicine, and it shares the rights to it with Vertex Pharmaceuticals (VRTX -2.10%). This therapy is important to CRISPR Therapeutics' prospects, but the company arguably has even more critical catalysts on the horizon.
Notably, the mid-cap biotech has several promising candidates in the pipeline that could make significant progress over the next few years. Let's discuss one of them: CTX310. Here's why this investigational medicine is, perhaps, even more important to CRISPR Therapeutics' future.
Image source: The Motley Fool.
A massive potential addressable market
Casgevy was no doubt a breakthrough, but its commercial opportunity is fairly limited. CRISPR Therapeutics and Vertex Pharmaceuticals have noted that the medicine currently has an addressable market of roughly 60,000 patients across several countries where it is approved, including the U.S., Canada, and several European and Middle Eastern countries.
But CRISPR Therapeutics' CTX310 -- which also utilizes the CRISPR mechanism -- could have a much larger market. This medicine is being designed to decrease LDL cholesterol and triglycerides (TGs), which, at high levels, can cause severe, sometimes life-threatening, cardiovascular and metabolic problems. So, it could reduce the risk of cardiovascular disease in eligible patients. There are approved medications to help patients lower TGs and LDL, most of which are taken once or twice daily.
Nothing wrong with that, but a one-time therapy that addresses this problem once and for all could be a significantly more convenient option than current standards of care. That's what CTX310 could be. What's the addressable opportunity for this medicine? According to CRISPR Therapeutics, more than 40 million patients in the U.S. alone have high LDL or TG levels.
$49.39-$0.60 (-1.20%)
NASDAQ · As of 4:00 PM ET 10/23/26
So, this medicine's commercial opportunity could be far larger than Casgevy's for the biotech, especially since CRISPR Therapeutics is developing it alone and won't have to share its profits with another drugmaker, as it does with Casgevy. CTX310 has, so far, posted encouraging results in clinical trials. In August, CRISPR Therapeutics reported data from a Phase 1a clinical trial in patients with high LDL or TG levels associated with certain genetic conditions. The medicine showed a mean TG reduction of 48% and a mean LDL reduction of 53% at the highest dose.
CRISPR Therapeutics will report data from a Phase 1b study in early November. There is still a long way before this therapy can hope to earn approval, but it is important to CRISPR Therapeutics' prospects, so it will be critical to monitor its clinical progress.
Is CRISPR Therapeutics' stock a buy?
CRISPR Therapeutics has underperformed the broader equity market over the past five years. But the company may bounce back in the medium term, provided it can make significant progress in its pipeline. The biotech has other candidates besides CTX310. For instance, it is working on a medicine called CTX611, an investigational, long-acting anticoagulant. Further, over the next five years, CRISPR Therapeutics could also make commercial progress with Casgevy, especially since a recent label expansion in patients as young as two added 5,500 people to its addressable market in the U.S.
Naturally, there is the very real risk of clinical and regulatory setbacks. Also, gene-editing medicines aren't exactly mainstream in the healthcare community yet, and there are some roadblocks to mass adoption, including their typically high prices and the fact that they are often very difficult to administer. All of these are risks worth factoring in. With all that said, is the stock a buy?
My view is that CRISPR Therapeutics is a fairly attractive biotech company, given its deep gene-editing pipeline that features several potential breakthrough medicines, but only for investors comfortable with significant risk and volatility. The stock might soar through 2030 if it can advance key pipeline programs and avoid commercial pitfalls, but certain setbacks might sink the share price. Invest accordingly.
How the tables have turned for small-reactor developer Oklo (OKLO -2.44%). In less than a year, Wall Street has changed its tune, from the enthusiastic rally cry of "Nuclear!" to a much less confident, almost incredulous, "Nuclear?" That change has wiped out not only 25% of the VanEck Uranium and Nuclear ETF (NLR -0.51%) but erased more than 60% of Oklo stock this year.
Therefore, Oklo has been down and up, down and up, down and up, tumbling and rising, like a shoe tossed around in a washing machine. The punishing rout, however, isn't all there is to Oklo stock right now. And if you stop at share price alone, you might miss what's actually happening in the nuclear business.
While Wall Street loses faith, Oklo persists
Oklo is a small reactor developer whose biggest market opportunity is AI power deals. As a company that's trying to rethink how power is delivered -- replacing large grid power with small modular nuclear reactors -- Oklo's technology aligns with the power needs of AI companies, whose enormous appetite for electricity is already straining local grids.
Image source: Oklo.
Delivering AI power has been Oklo's primary tailwind, but lately, it's been a headwind. Investors have been questioning whether money poured into AI infrastructure will actually deliver big returns. And for a company like Oklo, whose future depends on major infrastructure spending, that uncertainty has made investors more hesitant about the stock.
Add to that the fact that Oklo doesn't have regulatory approval for its Aurora powerhouse, and the stock's dismal 2026 performance makes a lot of sense.
Despite what the stock has done or failed to do this year, the company has been making some decent progress. Take, for example, the first criticality of its Groves test reactor in Texas, which was achieved in August. First criticality marks that Oklo built and started a nuclear reactor, a crucial first step for any nuclear operator.
Or how about the NRC's approval of the principal design criteria for its Aurora powerhouse in May, or the Department of Energy's approval of a preliminary safety analysis for Oklo's reactor in Idaho? Each is a small but crucial step toward commercialization.
$26.35-$0.66 (-2.44%)
NYSE · As of 4:00 PM ET 10/23/26
Oklo is making progress, but is it worth an investment right now?
Oklo has made substantial progress, but we shouldn't confuse progress with finances -- Oklo still manages an unprofitable business. It's still burning cash as it works toward commercializing its reactors. And though its first Aurora is planned to go live in 2028, there's no guarantee it will be live by that target year. Indeed, I wouldn't put firm trust in that data until construction is well underway, as Oklo has a history of repeatedly pushing back the predicted launch date of its first reactor.
If none of the above makes you flinch, a small speculative position in Oklo might be consistent with your investing approach. Less aggressive investors, however, will probably want to look elsewhere for their next growth stock.
Systém Starshield od SpaceX podle ukrajinského ministra obrany po desetidenním omezení, které narušovalo spojení vojenských dronů, opět funguje normálně.
Image Credits:Jagmeet Singh / TechCrunch SpaceX appears to have lifted restrictions the Ukrainian military’s of use Starshield — the military-grade version of the company’s Starlink internet system.
The Wall Street Journal reports that Defense Minister Evgeniy Khmara told reporters that Starshield appears to be working normally again, although the military is still conducting tests and has not received an explanation for the restrictions.
This follows a 10-day period where Ukrainian drones would lose internet connectivity when flying at speeds of around 100 miles per hour, resulting in the military losing control of some drones, while others became more vulnerable because they were flying more slowly.
President Donald Trump reportedly called SpaceX CEO Elon Musk on Wednesday and asked him to restore Starshield service. Both Trump and Musk have criticized Ukraine’s President Volodymyr Zelensky, with Musk recently posting, “Zelensky has gone too far.”
The WSJ previously reported that Musk ordered SpaceX to throttle Ukraine’s Starlink access, though some sources claimed he’d discussed it with the Trump administration first. Musk claimed in a post on X that Ukraine had “violated Starlink terms of service and used it for offensive drone strikes to kill people.”
“Were Starlink to be turned off, the Ukrainian front line would collapse immediately,” Musk said. “This is NOT a threat, it is simply a statement of fact.”
Apple má očekávaný dividendový výnos jen 0,3 %, tedy přibližně 1,08 USD na akcii ročně; k získání roční dividendy 100 USD je zapotřebí 93 akcií v hodnotě přes 32 000 USD.
There's certainly no denying this technology ticker has been a powerhouse performer for the past couple of decades. And yes, Apple (AAPL -0.14%) is technically a dividend-paying stock.
These two details alone, however, don't inherently make this name a well-suited choice for income-seeking investors.
The numbers
Don't misread the message. Again, Apple pays its shareholders an ever-growing dividend. It's just not a particularly big one. The stock's current forward-looking yield stands at a mere 0.3%. That's not much... only about $1.08 per share. To put those numbers in perspective, to collect just $100 worth of income from a stake in this popular company in a year, you'd need 93 shares of its stock. If you were buying that number at today's price, it would cost you a little over $32,000.
Image source: Getty Images.
Moreover, even if the company continues raising its dividend at its recent pace, in 10 years that initial $32,000 investment would still only yield annual dividends of just under $160. That translates into opportunity cost with making such a sizable commitment to AAPL as an income investment.
Not suited for this purpose
This doesn't mean Apple is a bad stock pick, to be clear. It's just not a great pick for income investors needing their assets to generate recurring, spendable cash at a reasonable rate of return.
Rather, AAPL remains primarily a growth stock, albeit a good one, boosted by even more generous stock buybacks. The company spent $25.8 billion on repurchases during the quarter ending in June, for perspective, while only $4 billion was spent funding its dividend payments. This dynamic isn't apt to change much under new CEO John Ternus' leadership, either.
AAPL Apple$347.73-$0.50 (-0.14%)
NASDAQ · As of 4:00 PM ET 10/23/26
So, if you're looking for a solid all-around income investment, look elsewhere, and start your search with stocks that have a higher yield. While a dividend yield at any particular time is far from a stock's whole story, it's certainly an important part of every income investment's profile.
James Brumley has no position in any of the stocks mentioned. The Motley Fool has positions in and recommends Apple. The Motley Fool has a disclosure policy.
SpaceX plánuje pro Colossus II převážně infrastrukturu Nvidia Vera Rubin a do druhého čtvrtletí chce nasadit 440 000 počítačů Vera Rubin pro trénování AI.
Space Exploration Technologies (SPCX +1.89%) just reported fabulous earnings, with a 161% increase in revenue and a $4.4 billion net income, its first quarterly profit.
Elon Musk shared exciting news about where the company's headed, including perfecting reusable spaceships and increasing satellite bandwidth by 100x. But he also gave fabulous news for Nvidia (NVDA -0.59%) investors.
Running on Rubins The standout in the report was the artificial intelligence (AI) business, now called SI, or Super Intelligence. Sales rose an astonishing 835% year over year, driven by compute deals, the acquisition of coding company Cursor, and enterprise adoption of the Grok AI model. It also became profitable, with $431 million in operating income.
Image source: Nvidia.
Musk boasted that he took the same team that made SpaceX's rocket business so dominant and tasked them with deploying AI compute infrastructure, likening it to "the New York Yankees playing in Little League" and calling it "not fair" to the competition.
The company rents out compute power from its massive Colossus I data center cluster, and it has agreements with Alphabet and Anthropic for $920 million and $1.2 billion in monthly revenue, respectively. It's now in the process of building Colossus II, and Musk said that it will predominantly feature Nvidia's Vera Rubin chip infrastructure.
He also said that SI plans "to have the most powerful training cluster online" by the second quarter, and to that end, it will need "440,000 Vera Rubin computers deployed for optimal training." Grok is growing quickly, with accelerating usage, and SpaceX is scaling it for enterprises. Musk sees them using Grok Bot, its AI agent, in roles as if it were a human agent. "I've never seen anything grow this fast," he said, and he anticipates Grok Bot being the main user of the extra compute.
The race to $1 trillion Musk thinks that SpaceX could have $500 billion to $1 trillion in Annual Recurring Revenue (ARR) by the end of 2027. If so, that would make it one of the biggest companies in the world by sales.
NVDA Nvidia$210.96-$1.25 (-0.59%)
NASDAQ · As of 4:00 PM ET 10/23/26
Nvidia CEO Jensen Huang gave a forecast of $1 trillion in sales through 2027 from the Blackwell and Rubin lines alone, and CFO Collette Kress said the company expects sales to increase 70% next year, although that's in a supply-constrained climate. Wall Street expects Nvidia sales to reach $692 billion next year, and that's with a 68% increase.
I would also note that Musk specifically said he's going to use Vera Rubin computers, not just Rubin chips. That's a full-stack computer system that brings in more revenue than chips alone.
That's great news for Nvidia and its shareholders, and it implies that there's still major upside for Nvidia stock over the next few years.
On its third quarter of 2026 earnings call, held on Oct. 22, 2026, Blackstone (BX -0.66%) reported $1.7 billion in distributable earnings, which is net cash available for dividends. Total assets under management, representing the market value of managed investments, reached $1.4 trillion. Three key takeaways from management highlight how the business is positioning for long-term growth.
1. Data Center Growth Relies on Long-Term Counterparty ContractsArtificial intelligence (AI) infrastructure requires massive capital to build computing capacity and power generation. The company mitigates execution risks by securing long-dated commitments from financially stable corporate clients before breaking ground.
At Blackstone, we approach investments in this area with the same rigor and focus on risk-adjusted returns that have defined our investment process for four decades. In AI infrastructure, for example, our data center portfolio is built on durable, long term contracts with highly creditworthy counterparties.
-- Stephen Allen Schwarzman, Chairman and Chief Executive Officer2. Wealth Channel Expansion Drives Steady InflowsIndividual investors are expanding allocations to alternative assets beyond traditional stock and bond portfolios. BXP, the company's flagship private equity vehicle for individual investors, reached $29 billion in net asset value (NAV), or total assets minus liabilities, in less than three years.
Of course, it is all about investment performance, and BXP has delivered, achieving an 18% net annualized return since inception.
-- Jonathan D. Gray, President and Chief Operating Officer3. Investment Grade Credit Captures Insurance DemandInsurance companies are turning to private markets to generate excess yield over public corporate debt. The company's investment grade private credit business, which provides high-quality debt financing, expanded 24% year over year to nearly $150 billion.
We have established the largest non-captive insurance platform in our industry, including 40 clients in our dedicated insurance solutions area representing leading global firms, of which over half expanded their relationship with us in the past 12 months.
-- Jonathan D. Gray, President and Chief Operating OfficerLooking AheadFee revenues and total assets under management are climbing across key investment strategies. Management is tracking the stabilization of real estate values alongside fee growth from new institutional funds amid surging bond yields and higher borrowing costs.
The firm delivered resilient financial results and overall fund performance in the third quarter, and for the first 9 months of the year, generated double-digit year-over-year growth across fee revenues, fee-related earnings, realized performance revenues, and distributable earnings -- all against a backdrop of significant external volatility.
-- Michael S. Chae, Vice Chairman and Chief Financial OfficerMassive scale across credit, infrastructure, and private equity provides structural advantages when originating complex deals. Long-term capital commitments give the firm steady management fees across market cycles.
I have learned the most important thing during these periods is to keep our focus on delivering great results for limited partners, pioneering new markets for investment, and expanding our fundraising channels, all of which are occurring now. Our firm has enormous earnings power, and we expect outstanding results in the years ahead
-- Stephen Allen Schwarzman, Chairman and Chief Executive OfficerThe Motley Fool has positions in and recommends Blackstone. The Motley Fool has a disclosure policy.
ADR společnosti Yiren Digital klesly 12. října 2026 o 44 % poté, co firma uvedla, že její výkonný předseda představenstva a generální ředitel Ning Tang podléhá trestněprávním donucovacím opatřením v souvislosti s vyšetřováním některých spřízněných subjektů ovládajícího akcionáře.
Why: Rosen Law Firm, a global investor rights law firm, continues to investigate potential securities claims on behalf of shareholders of Yiren Digital Ltd. (NYSE: YRD) resulting from allegations that Yiren may have issued materially misleading business information to the investing public.
So What: If you purchased Yiren 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/cases/yiren-digital-ltd/join 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 October 12, 2026, Yiren issued a press release entitled "Yiren Digital Provides Update on Its CEO and Operations." The press release stated that Yiren had "became aware of a police notice published on October 12, 2026, stating that Mr. Ning Tang, the Company's Executive Chairman and Chief Executive Officer, had been subject to criminal compulsory measures in connection with an investigation involving certain affiliates of the Company's controlling shareholder."
On this news, Yiren's American Depositary Shares fell 44% on October 12, 2026.
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 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 billions 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.
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Vertex získal společnost Crinetics Pharmaceuticals za 10 mld. USD, čímž rozšiřuje své zdroje tržeb mimo léčbu cystické fibrózy, která ve druhém čtvrtletí představovala 96 % jeho tržeb.
Vertex Pharmaceuticals' (VRTX -2.10%) stable of cystic fibrosis (CF) therapies is one of the biggest monopolies among biotech companies. The company was founded in 1989 and, after dabbling in infectious diseases, struck gold when it switched to genetic medicines.
Prior to Vertex's innovations, CF care was focused on clearing lung mucus, preventing infections, and managing symptoms. Vertex pioneered CFTR modulators, small-molecule drugs that target the underlying genetic defects in the CFTR protein that can cause cystic fibrosis.
Its first CF drug was CFTR modulator Kalydeco, which received Food and Drug Administration (FDA) approval in 2012. The company now has four CF therapies, led by the Trikafta/Kaftrio combination, which brought in $4.8 billion in sales through the first six months, and Alyftrek, which brought in $998 million through that period.
Of its $3.33 billion in second-quarter revenue, $3.2 billion came from CF therapies, about 96%. That ratio should soon change, however.
Image source: Getty Images
A breakout is already in progress
Vertex has said it is expecting $500 million or more in 2026 sales from non-opioid pain reliever Journavx and Casgevy, a gene-editing therapy developed with CRISPR Therapeutics (CRSP -1.20%), a potentially curative one-time treatment for severe sickle cell disease and another genetic blood disease, beta-thalassemia.
$523.93-$11.24 (-2.10%)
NASDAQ · As of 4:00 PM ET 10/23/26
Vertex also just released positive Phase 2b trial data on APOL1-Mediated Kidney Disease (AKMD) therapy inaxaplin. The company found that the oral therapy reduced protein leaking in urine, a leading sign of kidney damage, with no serious side effects. The patient pool for AKMD is unknown but is considered to be in the millions. The therapy is also being tested in a separate trial on patients with diabetes-related kidney disease.
Because no FDA-approved therapies target the genetic cause of AMKD, inaxaplin is positioned to capture first-in-class, first-mover market share. Analysts see the therapy as having the potential for at least $1 billion in annual sales.
The results in AMKD patients with moderate proteinuria may allow for a broader label for inaxaplin than previously expected. Vertex has already tested it in patients with focal segmental glomerulosclerosis (FSGS), a rare, severe, and destructive form of kidney disease where scar tissue forms on the glomeruli, the tiny filtering units of the kidneys. In the study, patients experienced a 43.4% reduction in urine albumin-to-creatinine ratio (UACR) after 13 weeks.
Its focus on other rare diseases could soon pay off
Looking beyond its recent trial with inaxaplin, Vertex has a large pipeline with several other promising late-stage candidates.
Povetacicept, acquired through its $4.9 billion purchase of Alpine Immune Sciences in 2024, positions Vertex in autoimmune conditions such as IgA nephropathy and generalized myasthenia gravis. It is an affinity-optimized Fc fusion protein. The drug has a Prescription Drug User Fee Act (PDUFA) date of Nov. 30, so it could be approved later this year or early next year.
The company is also testing zimloceucel, a stem-cell-derived therapy to treat type 1 diabetes. Its goal is to restore endogenous insulin production and potentially cure type 1 diabetes without requiring lifelong immunosuppression.
Its financial strength supports its pipeline expansion
The company's second-quarter revenue of $3.33 billion represents a 12% year-over-year rise. Vertex also raised its full-year revenue target to $13.1 billion to $13.2 billion, up from earlier guidance of $12.95 billion to $13.1 billion.
Earnings per share (EPS) were $4.31 in the quarter, up 8% over the same period a year ago. The company has solid cash flows, allowing it to close its largest acquisition to date on Sept. 1, a $10 billion purchase of Crinetics Pharmaceuticals, known for its endocrine disease therapies.
Crinetics' lead therapy is Palsonify, the only oral therapy approved for adults with acromegaly, a rare hormonal condition that causes some bones, organs, and other tissues to grow larger.
The purchase of Crinetics also brings along another promising late-stage therapy. Atumelnant is a once-daily pill to treat congenital adrenal hyperplasia, a rare endocrine condition that adversely affects the adrenal glands, which produce hormones that help regulate metabolism, the immune system, blood pressure, and other key functions. Atumelnant is also being tested to treat Cushing's syndrome.
Vertex is ready for the next step
The company's shares are up more than 15% so far this year, but considering its growth potential, that doesn't appear to be just from hype. Vertex has increased annual revenue by more than 600% over the past decade and has used profits from its CF franchise to broaden its base into other rare-disease areas.
The Crinetics purchase is expected to take years to pay off, but Vertex is sticking to a proven game plan by purchasing therapies that target severe diseases in which the underlying biology is well understood, patient populations are concentrated, and existing treatment options are severely lacking.
This exact strategy is what turned its CF business into a massive financial success. Beyond aligning with its core philosophy, the acquisition provides Vertex with new revenue streams beyond its CF treatments.
Kinder Morgan má 67% expozici vůči zemnímu plynu oproti 35 % u společnosti Energy Transfer, a je tak lépe připraven těžit z růstu poptávky po elektřině v souvislosti s AI.
Energy Transfer (ET +2.05%) and Kinder Morgan (KMI +2.11%) are two of the largest midstream businesses in North America. Although both have cut their dividends in the past, they are growing them at a steady clip today. However, as artificial intelligence (AI) shifts the demand story in the electricity sector, Kinder Morgan is likely the better-positioned business, if you're willing to pay for it. Here's what you need to know to choose between these two midstream operators.
What does the midstream have to do with AI? There is a massive effort underway to build the infrastructure that supports artificial intelligence. However, at its core, AI is just a fancy computer program. It doesn't exist without electricity. The more AI infrastructure that's built, the more electricity is needed. Between 2024 and 2030, the International Energy Agency expects electricity demand from AI to increase "more than four times faster than the growth of total electricity consumption from all other sectors."
Image source: Getty Images.
The world needs more electricity in a big way, with some estimates that electricity demand will grow by 60% between 2025 and 2045. That's up from growth of just 10% between 2005 and 2025. Pipeline companies are a vital part of supplying this electricity because natural gas is increasingly being used to generate power.
There's more good news. Businesses like Energy Transfer and Kinder Morgan largely charge fees for the use of their energy infrastructure assets. So while commodity prices can be highly volatile, midstream companies largely sidestep that risk. The volume flowing through their systems is more important than the price of what is being moved. In other words, Energy Transfer and Kinder Morgan are likely to benefit from AI regardless of what happens to natural gas prices.
$34.43+$0.71 (+2.11%)
NYSE · As of 4:00 PM ET 10/23/26
Which is better positioned: Energy Transfer or Kinder Morgan? There is a notable difference between Energy Transfer and Kinder Morgan regarding natural gas. Natural gas makes up around 35% of Energy Transfer's business, while Kinder Morgan's exposure is 67%. In fact, Kinder Morgan claims to own the largest natural gas transmission network in the United States.
From this perspective, Kinder Morgan is better positioned to benefit from increasing demand for the natural gas used to generate electricity. If that is all you are focused on, it is probably the better choice for your portfolio.
ET Energy Transfer$20.45+$0.41 (+2.05%)
TXSE · As of 4:00 PM ET 10/23/26
The problem is that Kinder Morgan's dividend yield is only 3.4%, which is far below the 6.7% yield that you could collect from Energy Transfer. To buy either for a dividend portfolio, you need to accept that both have both cut their dividends in the past. They are growing again, as noted above. In fact, slow and steady dividend growth is likely to be the norm for each at this point. Still, if income is your real focus, then Energy Transfer is the obvious winner. And, while it may not benefit as much as Kinder Morgan from AI's voracious appetite for electricity, it will still benefit.
What are you really trying to achieve? The simple answer here is that Kinder Morgan is more leveraged to natural gas than Energy Transfer. But that's looking at the comparison in something of a vacuum. Wall Street clearly knows Kinder Morgan is tied into the AI story, and it has been priced accordingly. That has left the stock with a relatively low yield in a sector known for providing attractive yields. In other words, if you are trying to live off of the income your portfolio generates, you may be better off with less natural gas exposure and more yield. And that could make Energy Transfer the more appropriate choice.
Axon Body 5 delivers 25x the AI processing power of earlier-generation cameras, with upgraded connectivity, audio and battery life to support real-time situational awareness in the field
, /PRNewswire/ -- Axon (Nasdaq: AXON), the global leader in public safety technology, today announced Axon Body 5, its newest body-worn camera designed to bring more powerful intelligence, connectivity and real-time support directly to officers in the field.
For years, Axon body cameras have helped agencies capture critical evidence and create greater transparency. Body 5 is built to help officers during the call, with information, assistance and backup on the spot.
Axon is introducing two versions of its latest flagship camera: Axon Body 5 and Axon Body 5 Pro.
New Axon Body 5 delivers 25x the AI processing power of earlier-generation cameras. "Officers shouldn't have to choose between getting information and watching the scene. With Axon Body 5, they don't," said Rick Smith, Axon Founder and CEO. "They capture a license or document with the camera, keep their hands free and eyes up, and get information faster than writing it down and calling it in by radio. An officer fully engaged with the person in front of them, not down at a notepad, is a safer officer and a better-served community."
Axon Body 5: Built for the AI Era
Built from the ground up for the AI era, Axon Body 5 delivers 25x the AI processing power than earlier generation Axon body cameras, alongside advancements in connectivity, audio, video and battery life. Together, these upgrades give the camera the physical power to run smarter AI features — both today and as new AI tools are developed in the future — while also making it more dependable for officers to use every day.
For the first time, Axon is also introducing two versions of its latest flagship camera: Axon Body 5 and Axon Body 5 Pro.
Both models feature several key advancements, including:
25x more processing power for AI: A powerful new computing architecture creates the capacity to support current and future AI features directly on the body camera. Enhanced video: Improved video captures clearer evidence across challenging environments, including better low-light performance. Improved connectivity: Seamless connectivity in urban and remote environments - and more precise location capability - helps officers, cameras and remote support teams stay connected when timely information matters most. Longer battery life: 20% more battery life than the previous generation helps keep the camera ready and connected throughout an officer's shift. The Axon Body 5 Pro will continue to gain new AI capabilities as they become available, growing along with the AI Era Plan. Additionally, new hardware features include:
A near-focus camera: An additional dedicated camera lens lets officers scan driver's licenses to check status and search for wants or warrants in seconds, without returning to the patrol vehicle, with relevant information sent to Axon Fusus to support real-time operations. Front-facing speakers: Four additional speakers project even more powerful audio toward the person an officer is speaking with, helping real-time translations from Axon Assistant carry more clearly over heavy traffic or crowd noise. Additional memory: Extra space lets the camera run several AI tools at once, helping officers stay better informed and work faster. Bringing More of Axon's AI Era Into the Field
Axon Body 5 helps officers get more out of the Axon AI Era Plan by bringing smart tools right to the scene. Axon's portfolio already supports public safety professionals across a growing range of tasks. For example, Draft One helps officers turn body-camera audio into high-quality report drafts and Axon Assistant provides voice-based information access and real-time translation.
Increasingly, Axon is also bringing AI into real-time operations.
Axon Guardian is a new category of AI features within the AI Era Plan that was specifically created to work with an officer's field-based devices - starting with body cameras and in-car cameras - to improve safety. Guardian is designed to flag potential risks as situations unfold and create alerts when additional attention may be needed. Two of the first features include:
Escalation Detection: When an Axon Body 4 or Axon Body 5 camera is activated and recording, Guardian has the ability to detect potential conflicts in real time and create an alert in Axon Fusus. A human reviews the livestream and decides if additional support or action is needed. Approach Alert: When active on Axon Fleet 3, Guardian can detect if the door of a stopped vehicle opens and alert the officer through the in-car display and their body-worn camera. Combined, Axon Body 5 and the expanding AI Era portfolio demonstrate the importance of AI as a critical resource to assist public safety professionals before, during and after an incident — reducing administrative burden, improving situational awareness and helping protect more lives.
Innovating Responsibly
Axon's Responsible Innovation framework guides the development of all of its products. Designed with this in mind, Axon Body 5 and Guardian prioritize human oversight and maintain agency control over data. As a key part of the responsible innovation process, Axon's independent Ethics and Equity Advisory Council was created to help responsibly develop and deploy new technologies with transparency, while aligning with community expectations.
General availability dates for Axon Body 5 and Axon Guardian will be announced soon. Product features and capabilities vary by configuration. For more information on Axon's current products and services: Axon Product Catalog - Axon.com.
About Axon
Axon (Nasdaq: AXON) is the global leader in public safety technology supporting state, local, federal and international public safety agencies with technology designed to Protect Life. Complementing its mission, Axon's growing Enterprise market focuses on protecting critical infrastructure and frontline workers across multiple industries including corporate security, hospitality, retail and healthcare. Founder-led since 1993, Axon builds products with transparency and responsibility. From TASER energy devices to today's connected network of hardware - including cameras, drones, and robotics - cloud software, sensors, and AI-tools, the Axon ecosystem helps seamlessly protect people and places when it matters most. To ensure these technologies align with community expectations, Axon's independent Ethics & Equity Advisory Council guides the ethical, inclusive, and accountable design of its products and services. Learn more about the EEAC and Axon's Responsible Innovation framework at Axon Responsibility.
Non-Axon trademarks are the property of their respective owners. Axon, TASER and the Delta Logo are trademarks of Axon Enterprise, Inc., some of which are registered in the US and other countries. For more information, visit www.axon.com/legal. All rights reserved.
Please visit https://investor.axon.com and https://www.axon.com/newsroom for more information.
Media Contact:
Kate MacKinnon
Vice President, Communications
[email protected]
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Peter Thiel said that after Steve Jobs died in 2011, Apple hasn't innovated. Justin Sullivan/Getty Images Peter Thiel, evidently, isn't a fan of the iPhone Duo.
In fact, the billionaire PayPal cofounder and tech investor said he hasn't been very impressed with much of anything that Apple has done since its eccentric founder, Steve Jobs, died of cancer in 2011.
"In my telling, it did nothing new after Jobs," Thiel said of the iPhone maker in a September interview with author Walter Isaacson for the "Builder's Podcast," which was released on Thursday.
"It turned out, yeah, the mobile phone was this giant invention — there was not that much more to do," he said. "Then it was just scaling and branding and building it out over 15 years or whatever."
Indeed, Apple has faced criticism for failing to innovate beyond the mobile phone and tablet, especially in the age of AI, where its "Siri" product is not as advanced as rivals from ChatGPT or Anthropic.
Peter Thiel says Apple has done 'nothing new' after Steve Jobs
Jobs unveiled the first iPhone back in 2007 at a conference in San Francisco. Nearly 20 years later, Apple released the 18th iteration this week, with one slight caveat: This one folds.
That said, MacBooks are the de facto laptops for many an AI-nerd and normie alike. iPhones are ubiquitous, and the sleek AirPods design took hold when they were released in 2016.
Though Thiel told Maureen Dowd of The New York Times in 2017 that Apple's era was over, the company's stock price has grown steadily since then.
Thiel didn't pooh-pooh Apple entirely. He called it a "pure, well-run value stock," but lamented what he described as the loss of vision after Jobs' death.
"I would still say somehow Elon or Steve Jobs are way better for society than Tim Cook," he said.
Apple didn't immediately respond to a request for comment sent on Saturday.
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Truman Dickerson is the Weekend News Fellow at Business Insider, based in New York City. He covers trending tech and business news. He previously reported for The Boston Globe's Express Desk. He graduated from Boston University, where he served as editor in chief of The Daily Free Press, BU's student-run newspaper.Contact him at [email protected]
Meta Platforms oznámila split akcií prostřednictvím vytvoření akcií třídy C bez hlasovacích práv; ve 3. čtvrtletí zvýšila tržby meziročně o 26 % na 64,6 mld. USD.
A stock split is a corporate action in which a company increases the number of shares it has outstanding by dividing existing shares into multiple shares and proportionately decreasing its share price. Stock splits don't change a company’s intrinsic value, but they can garner significant attention because they make each share more affordable, potentially increasing trading activity.
And the latest major corporation on Wall Street to announce a stock split is none other than Meta Platforms (META -0.96%). The tech leader has beaten the broader equity market since its 2012 IPO, gaining a little over 1,700%. Yet, the stock still has outstanding long-term prospects.
Image source: The Motley Fool.
Meta's strong third-quarter updateMeta Platforms announced its stock split alongside its third-quarter results. The split wasn't the best part of the company's update: Meta's financial performance during the period was pretty strong. Meta Platforms' revenue increased by 26% year over year to $64.6 billion.
True, the company's operating income dropped by 37% year over year to about $13 billion, but that was largely due to legal-related expenses. Meta recorded a $9.89 billion charge because of a recent legal settlement. Without that, the company's operating income would have increased by 11% year over year.
Besides, the legal settlement was worth the trouble. Meta Platforms agreed to pay up to $18 billion (with $12.7 billion guaranteed and $5.3 billion contingent on certain conditions) over 10 years to a bipartisan coalition of attorneys general representing dozens of U.S. states and territories in connection with lawsuits alleging that Meta's social media platforms have harmed consumers.
The amount is by no means catastrophic, especially considering the time frame. Returning to Meta's third-quarter results, the company posted earnings per share of $3.83, up 265% year over year, as the company's provision for income taxes dropped significantly. Meta also made progress elsewhere.
For instance, the company's daily active people across its websites and apps rose 3% year over year to 3.64 billion. Now turning to Meta's planned stock split, the company will create a new Class C non-voting common stock and issue one Class C share for each outstanding share.
The company emphasized that it is making this move to help raise capital. The tech giant could fund various activities by issuing Class C shares without diluting CEO Mark Zuckerberg's voting control. Meta's main motivation for doing this is clear: the company is looking to fund its aggressive artificial intelligence (AI) ambitions to tap into what it sees as a large market opportunity.
META Meta Platforms$642.62-$6.23 (-0.96%)
NASDAQ · As of 4:00 PM ET 10/23/26
The AI tailwindMeta made significant AI-related progress during the third quarter. For instance, the company released Muse, a consumer-facing AI agent that was an instant hit. Meta noted that more than 10 million people in the U.S. and Canada have set up Muse, and about 25% use it on any given day.
The company also reported that Muse is particularly popular as a shopping assistant, which is important given that one of Meta's plans to monetize the agent is to charge retailers small per-transaction fees.
Retailers only have an incentive to pay these fees if Muse-related shopping generates significant revenue for them. So, engagement with the personal agent will be critical to track. Meta still has a long way to go.
The company wants Muse to reach billions of people, and it will continue to invest to make that goal a reality. And if Meta can get there -- or even somewhere close to that target -- it will help boost the company's revenue and profits over the long run.
The company has also released a small-business version of Muse, as well as Muse Wonder and Muse Wonder Full, advanced AI agent models designed to handle tasks in expert domains, such as law and finance. Significant utilization here could also be a major boost to the business.
Of course, Meta's core ad business remains healthy and continues to generate most of the company's revenue. But Meta has a clearer path to a more diversified revenue stream than it has had in a long time, and that should excite investors.
Despite the fears that the company's AI investments would harm the business, the tech leader seems to have found a way to turn it into an advantage, and there is more where that came from. Meta isn't done delivering market-beating returns.
Halper Sadeh prověřuje prodej společnosti GoPro společnosti Starman Optical za 1,14 USD za akcii, s možnou úpravou o čistý pracovní kapitál při uzavření transakce.
GPRO Stock Alert: Halper Sadeh LLC is Investigating Whether GoPro, Inc. is Obtaining a Fair Price for its Shareholders
Halper Sadeh LLC, an investor rights law firm, is investigating the sale of GoPro, Inc. (NASDAQ: GPRO) to Starman Optical, Inc. for $1.14 per share, subject to potential adjustment based on GoPro’s net working capital at closing.
Halper Sadeh encourages GoPro shareholders to click here to learn more about their rights and optionsor contact Daniel Sadeh or Zachary Halper free of charge at (212) 763-0060 or [email protected] or [email protected].
The investigation concerns whether GoPro and its board of directors violated the federal securities laws and/or breached their fiduciary duties by failing to: (1) obtain the best possible price for GoPro shareholders; (2) conduct a fair sales process free of any conflicts of interests; and (3) disclose all material information for GoPro shareholders to evaluate the transaction.
On behalf of shareholders, Halper Sadeh LLC may seek increased consideration, additional disclosures, or other relief and benefits.
Halper Sadeh LLC represents investors all over the world who have fallen victim to securities fraud and corporate misconduct. Our attorneys have been instrumental in implementing corporate reforms and recovering millions of dollars on behalf of defrauded investors.
Attorney Advertising. Prior results do not guarantee a similar outcome.
View source version on businesswire.com: https://www.businesswire.com/news/home/20261024651501/en/
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I/we have no positions in any stocks mentioned, and have no plans to buy any new positions in the stocks mentioned within the next 72 hours.
Honeywell po vyčlenění letecké divize do samostatné společnosti zvýšil celoroční výhled tržeb i zisku; ve 3. čtvrtletí dosáhl objem nevyřízených zakázek téměř 19 miliard USD.
On its third quarter of 2026 earnings call, held on Oct. 22, 2026, Honeywell (HON +1.30%) raised its full-year profit and sales outlook after completing the spin-off of its aerospace business. The shift leaves the business as a pure-play automation enterprise holding an order backlog, or total value of unfulfilled customer bookings, of nearly $19 billion in Q3.
Shareholders now own a more focused operation with higher cash conversion and fewer overhead drags. Three things management said on the earnings call stand out.
1. Process Automation Order Backlog Signals a Multiyear Energy ExpansionIndustrial customers in the Middle East and Africa are pouring cash into plant upgrades. That investment drove double-digit backlog growth in process automation and technology, the segment that supplies industrial control systems. That accumulated pile of unfulfilled contracts gives the company multiyear sales visibility as energy producers build out refining capacity and liquefied natural gas (LNG), which is gas cooled to liquid for transport.
We continue to believe that the ongoing transition to LNG and renewables as a priority fueled increasing pipeline activity from refurbishment and rebuilds in Middle East, and the refining build out in Africa will drive a meaningful energy upcycle over the next several years.
-- Vimal Kapur, Chairman and Chief Executive Officer2. Eliminating Stranded Corporate Overhead Ahead of Schedule Expands MarginsManagement eliminated stranded costs, or corporate overhead expenses left behind after spinning off the aerospace unit, six months faster than original targets. That rapid fixed-cost takeout helped segment profit margins, or the percentage of revenue remaining after direct operating expenses, rise by nearly four percentage points to over 21%. Removing those corporate drags allows more gross revenue to flow straight to net profits.
Importantly, with accelerated progress this quarter, we now expect to eliminate all remaining stranded costs by the end of '26, just six months after the aerospace spin-off, demonstrating our strong execution capabilities.
-- Vimal Kapur, Chairman and Chief Executive Officer3. Data Center Infrastructure Demand Drives Double-Digit Order GrowthData center operators are expanding fast and doubled their year-to-date order volumes for process control systems and building management software. Honeywell is capitalizing on that boom by bundling its physical equipment with Forge, its internal software platform that monitors facility efficiency and maintenance. That software integration secures higher recurring revenue, which represents predictable subscription income, while deepening customer lock-in.
We saw year to date orders growth of more than 100%. Based upon the pipeline visibility we have, we expect very high growth in 2027 also.
-- Vimal Kapur, Chairman and Chief Executive OfficerLooking AheadOrder velocity across energy infrastructure and data centers is accelerating. That demand pushed free cash flow conversion, or net profit converted to cash, to 95% in Q3, and Honeywell expects this to be above 100% in Q4.
Rapid debt reduction expands balance sheet flexibility and gives leadership clear capital allocation choices, which includes possible mergers and acquisitions (M&A).
Importantly, the cash generation and continued reduction in our leverage will increase our capital allocation flexibility, including capacity to pursue disciplined M&A.
-- Michal Stepniak, Senior Vice President and Chief Financial OfficerLower corporate expenses and disciplined pricing position the business for sustained operational performance.
With our performance this quarter and backlog of nearly $19 billion, we are confidently raising our 2026 outlook across all metrics setting up for a strong start to 2027.
-- Vimal Kapur, Chairman and Chief Executive OfficerThe Motley Fool has positions in and recommends Honeywell Technologies. The Motley Fool has a disclosure policy.
Union Pacific ve třetím čtvrtletí 2026 dosáhla rekordních výsledků; objem domácí intermodální přepravy vzrostl o 13 % a společnost tak zaznamenala páté rekordní čtvrtletí v řadě.
On its third quarter of 2026 earnings call, held on Oct. 22, 2026, Union Pacific Corporation (UNP -1.75%) reported record financial results driven by volume growth across its freight network. Long-term investors care because operational efficiency and network capacity let the railroad grow margins as volume expands over time. Three things management said on the earnings call stand out.
1. Operational Discipline Keeps Terminal Dwell Times LowOperational efficiency determines how fast freight cars cycle through rail yards. Management reduced terminal dwell, the time train cars spend idling in yards before moving, below 20 hours for four straight quarters, enabling the network to handle 6% higher volume without operational drag.
Freight car velocity increased 1% to 228 miles per day, driven by a 2% improvement in terminal dwell. This marks our fourth straight quarter of terminal dwell below 20 hours, demonstrating our ability to run an efficient network while handling higher demand.
-- Eric Gehringer, Executive Vice President of Operations2. Proposed Norfolk Southern Combination Aims to Lower Supply Chain CostsCombining rail networks with Norfolk Southern creates a transcontinental system connecting Western and Eastern markets without handoffs. Eliminating interchange delays reduces transit times for shippers, making rail transport far more competitive against long-haul trucking.
It will lower transportation costs and provide faster, more seamless rail service options that enable our customers to compete and help keep goods affordable for American consumers.
-- Jim Vena, Chief Executive Officer3. Domestic Intermodal Business Drives Record Volume GrowthDomestic intermodal shipments, which involves moving freight containers via truck and train, reached a fifth consecutive record quarter as shippers converted highway truck traffic to rail. Service reliability and buffer resources enabled the company to capture market share from highway carriers.
Domestic intermodal delivered its fifth consecutive record quarter in both volume and revenue. Our foundation of service, combined with strong business development and the deployment of buffer resources, enabled 13% volume growth.
-- Kenny Rocker, Executive Vice President of Marketing and SalesLooking AheadFreight demand accelerates across intermodal and industrial markets, and leadership isn't hiding its satisfaction about network execution. Maintaining buffer locomotives and trained crews provides capacity to handle surge traffic smoothly.
We feel very confident that we have sufficient resources that we can deploy and continue to handle the growth seamlessly and continue to put up the great numbers, the record results that we have done so far. But we are wanting to make sure we maintain that surge buffer.
-- Jennifer Hamann, Chief Financial OfficerManagement is watching core operating ratio, an efficiency metric showing expenses as a percentage of revenue, to ensure pricing discipline offsets diesel cost swings. Long-term value rests on leveraging train length efficiency, terminal technology, and single-line service advantages to win freight from highways.
Overall, we are delivering strong financial results in 2026 as we consistently execute on the three key levers for our railroad success: volume, pricing, and productivity.
-- Jennifer Hamann, Chief Financial OfficerThe Motley Fool recommends Union Pacific. The Motley Fool has a disclosure policy.
A wave of investor enthusiasm for enterprise artificial intelligence workflow tools sent Appian (APPN +2.35%) soaring 24.2% this week.
Appian stock changed hands at $52.35 as of the close on Friday, Oct. 23, up 27.2% this week from Friday, Oct. 16's close, according to data provided by S&P Global Market Intelligence. Over the same period, the S&P 500 (^GSPC -0.52%) fell 0.5%, and the Nasdaq-100 fell 0.7%.
Image source: Getty Images.
AI agent controls and pre-earnings momentum drive the rallyAppian released product updates showcasing tools that give enterprise customers tighter control over automated AI agents, helping businesses run processes safely. The product news coincided with broader sector coverage highlighting Appian's strong operational momentum following its second-quarter performance, where the company generated $203.3 million in revenue--up 19.1% year over year--and delivered an elevated full-year outlook.
APPN Appian$52.35+$1.20 (+2.35%)
NASDAQ · As of 4:00 PM ET 10/23/26
Appian sells low-code software that allows businesses to build automated workflows and integrate artificial intelligence agents into their operations. Its platform connects data across disparate corporate systems, enabling enterprise clients, including financial institutions and government agencies, to automate complex operational tasks.
Appian trades at a price-to-sales (P/S) ratio of 4.9. The company generated $203.3 million in its last reported quarter ending June 30, 2026, but posted a net loss of $11.8 million, underscoring its ongoing push toward sustained profitability. This week's momentum shifts the near-term focus to whether Appian can convert its new enterprise AI features into accelerated subscription growth.
What to watch next for AppianInvestors will not have to wait long for an operational checkup. Appian plans to release its third-quarter 2026 financial results before the market opens on Thursday, Nov. 5, 2026.
Key items to watch include acceleration in subscription revenue and progress toward GAAP profitability. As of June 30, 2026, Appian held $167.9 million in cash and short-term investments against $295.3 million in total debt, including lease obligations, making consistent cash flow generation an important long-term milestone.
Is Appian stock a buy?While Appian stock powered higher this week, those who have had it on their radars shouldn't feel that the recent rise means that shares are too pricey to consider. Trading at 4.9 sales, Appian stock is priced at a slight premium to its five-year average P/S of 4.6 -- hardly a valuation that should preclude growth investors from clicking the buy button.
Of course, investors will want to see what the company reports for Q3 2026 financial results in the coming weeks. Either a slowdown in revenue growth or a significantly steeper net loss would both (or merely one of these) signal that an investment bears a lot more risk and that investors should proceed cautiously.
Akcie Hasbro tento týden po výsledcích za 3. čtvrtletí vzrostly o 18,9 %: tržby stouply o 15 % na 1,60 mld. USD, především díky 34% růstu hry Magic: The Gathering.
A blowout third-quarter earnings report driven by record card-game sales sent Hasbro (HAS +0.18%) surging 18.9% this week.
Hasbro stock changed hands at $117.44 as of the close on Friday, Oct. 23, up 18.9% from Friday, Oct. 16's close. Across those five sessions, the S&P 500 (^GSPC -0.52%) was down 0.5%, and the Nasdaq-100 was down 0.8%.
Magic: The Gathering and guidance expansion drive the rallyHasbro delivered a strong third quarter, posting revenue of $1.60 billion, up 15% year over year beating consensus estimates of $1.48 billion. Adjusted earnings per share (EPS) hit $2.90, comfortably beating the $1.86 Wall Street expectation. Robust operating cash flow of $907.3 million through nine months prompted management to double its annual share repurchase goal from $200 million to $400 million.
Hasbro designs, manufactures, and licenses play assets, tabletop games, and digital entertainment, selling globally to mass-market retailers, specialty hobby shops, and digital platforms. The company owns major brands like Monopoly and Transformers, but tabletop card franchise Magic: The Gathering served as the main engine this quarter. Magic revenue jumped 34% year over year to exceed $600 million for the first time, while tabletop gaming sales grew sharply.
High-margin licensing and cost discipline added extra momentum, contributing $105 million in savings through the first nine months toward a $150 million annual goal. This week's guidance raise confirms that high-margin digital and tabletop gaming licenses are successfully shifting Hasbro's profit engine away from lower-margin traditional toy manufacturing.
Image source: Getty Images.
What's next for HasbroHasbro trades at a trailing price-to-earnings (P/E) ratio of 17.3, reflecting investor optimism around expanding profitability. Management raised its full-year constant-currency revenue growth target from a midpoint of 6% to a new range of 7%-9%, and increased operating margin expectations.
Looking ahead, investors will watch how the holiday shopping season impacts traditional consumer toy sales. Management noted that fourth-quarter Magic revenue could dip in the low- to mid-single-digit range due to product release timing. However, two major digital video game launches remain slated for 2027. Hasbro expects to report its next quarterly earnings in early February 2027.
HAS Hasbro$117.44+$0.21 (+0.18%)
NASDAQ · As of 4:00 PM ET 10/23/26
Is Hasbro Stock a Buy?While a P/E of about 17 doesn't seem excessive, it does represent the highest level for Hasbro stock in the last year. That's because the company is firing on all cylinders. Magic: The Gathering revenue surged 34% year over year in Q3, breaking last quarter's record. The company also plans to launch two more digital games in 2027, Exodus and Warlock.
Hasbro's strong cash flow enabled it to double its yearly share buyback plans. Investors could do well to follow management's lead.
There are risks, of course. Hasbro depends on Magic: The Gathering for nearly 90% of its operating profits. That's a lot of single-franchise risk. Its core toy and consumer products business is also vulnerable to economic downturns or weak consumer spending.
For long-term investors, though, Hasbro should be a good stock to own. It's particularly suited to helping young adults learn more about investing, by owning a stock they may be familiar with. Parents who want to give a stock to a child or a teen who is just starting to invest could do well to choose Hasbro.
CBRE očekává, že tržby z infrastrukturních služeb v roce 2027 dosáhnou téměř 7 mld. USD, což by oproti letošnímu roku představovalo nárůst o více než 40 %.
On its third quarter of 2026 earnings call, held on Oct. 22, 2026, CBRE (CBRE -6.05%) maintained its full-year core earnings per share (EPS) guidance range of $7.80 to $7.90. Understanding how the commercial real estate services enterprise navigates high interest rates provides a window into its shift toward contractual income sources. Three takeaways from management explain how the company is positioning itself for long-term growth.
1. Infrastructure Services Are Set to Reach $7 Billion in RevenueCBRE is expanding beyond traditional commercial real estate into technical infrastructure services like mechanical, electrical, and plumbing (MEP) projects for data centers. Management expects this expansion to drive total infrastructure revenue to nearly $7 billion in 2027.
Taking this work into account, we expect our total infrastructure services revenue to reach nearly $7 billion in 2027, growing more than 40% from this year.
-- Robert Sulentic, Chair and Chief Executive Officer2. Resilient Business Lines Neutralize Real Estate Capital Market HeadwindsHigher interest rates continue to depress property sales and mortgage origination across the commercial real estate sector. Contract-based operations in facilities and project management provide steady cash flow that offsets transaction volatility.
I do want to say this is a great example of how our business model is working the way we've intended and the way we've shaped it. Even in an environment where our capital markets businesses are slowing, our resilient businesses are able to offset that and deliver double-digit growth.
-- Emma Giamartino, Chief Financial OfficerManagement is prioritizing targeted mergers and acquisitions (M&A) in high-growth areas over buying back company stock. CBRE reduced share buybacks in the third quarter to fund transactions in the data center sector.
So we're always continuing to prioritize M&A. You saw that with Onnec. And you saw in Q3 that we did slow down our buyback somewhat in anticipation of this deal. And you should expect that to continue through the fourth quarter.
-- Emma Giamartino, Chief Financial OfficerLooking AheadInterest rate volatility is delaying property deals, yet stabilizing borrowing costs should eventually restore momentum across real estate capital markets.
What we really need is for rates to stabilize. The volatility and the uncertainty is what's driving a pause or a hold or even delaying deals to 2027. And we expect that stability to come in the back half of next year.
-- Emma Giamartino, Chief Financial OfficerGlobal scale, deep client ties, and broad service diversification allow CBRE to manage cyclical shifts while maintaining pricing discipline. Expanding data center capabilities and recurring facilities revenue reinforce long-term earnings durability despite the impact of rising interest rates.
We are seeing competing dynamics in our business. We expect to see continued outsized growth in our infrastructure businesses. This will be somewhat offset by lower growth in our real estate capital markets-driven businesses. As a result, we continue to see a path to 15% core EPS growth in 2027.
-- Emma Giamartino, Chief Financial OfficerThe Motley Fool has no position in any of the stocks mentioned. The Motley Fool has a disclosure policy.