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Applied Digital Corp. is a technology company, which engages in the provision of development and operation of data centers which provide computing power. It operates through the Data Center Hosting Business and HPC Hosting Business segments. The Data Center Hosting Business segment provides energized infrastructure services to crypto mining customers. The HPC Hosting Business segment focuses on the designing, constructing, and operating data centers tailored to support high power density applications like HPC and AI. The company was founded by Wesley Carl Cummins and Jason Zhang in May 2001 and is headquartered in Dallas, TX.

Applied Digital Corporation

APLD is trending due to positive earnings, a raised price target from Needham, and news of a massive AI lease deal with CoreWeave. The community is discussing the potential for a short squeeze and future hyperscaler deals, with some bulls projecting significant gains while bears warn of overvaluation. Overall, sentiment is bullish, driven by the company's growth in the AI data center space.

IonQ, Inc. develops and manufactures quantum computers. The firm specializes in quantum computing and quantum information processing. The company was founded by Christopher Monroe and Jung Sang Kim in 2015 and is headquartered in College Park, MD.

IonQ Inc

IONQ is trending due to a recently announced $2 billion equity offering, leading to community debate about dilution and valuation. While some view the offering, priced at a premium, as a bullish sign of investor confidence in the quantum computing company's future, others express concerns about the long-term impact on shareholders and the sector's high valuations.

SEALSQ Corp. is a holding company, which engages in the security of microcontrollers. It operates through the following geographical segments: North America, Europe, Middle East, Africa, Asia Pacific, and Latin America. It focuses on authentication process, digital certification, and covering individual patents of semiconductors. The company was founded on April 1, 2022 and is headquartered in Cointrin, Switzerland.

SEALSQ Corp

SEALSQ Corp is trending due to a strategic partnership focused on developing quantum-resistant chips for U.S. defense applications, igniting discussions about future government contracts. The community is actively evaluating the company's growth potential relative to other quantum computing stocks. Many investors are describing LAES as undervalued with potential for a significant upward trajectory.

TeraWulf, Inc. owns and operates fully integrated environmentally clean bitcoin mining facilities in the United States. TeraWulf will generate domestically produced bitcoin powered by nuclear, hydro and solar energy. The company was founded by Paul Prager and Nazar Khan on February 8, 2021 and is headquartered in Easton, MD.

TeraWulf Inc

TeraWulf is trending as investors discuss the potential for a short squeeze, fueled by high short interest and recent positive developments, including a partnership with Google. Community members are closely monitoring resistance levels and anticipating a breakout, drawing comparisons to other AI and high-performance computing data center plays. The focus remains on the company's transition towards AI infrastructure and its potential for growth in the sector.

Rigetti Computing, Inc. provides full-stack quantum computing services. It serves global enterprise, government, and research clients through its Rigetti Quantum Cloud Services platform. The company was founded by Chad Rigetti in 2013 and is headquartered in Berkeley, CA.

Rigetti Computing Inc

RGTI is trending as traders debate whether its recent surge is justified by fundamentals or fueled by a short squeeze, with community members highlighting both bullish and bearish arguments.  The launch of a new 2x short ETF (RGTZ) has added another layer to the discussion, as some believe it will exacerbate the squeeze while others see it as a sign of an impending reversal.  Quantum computing stocks are also in focus, and the community is comparing RGTI's valuation and potential against competitors.

Rocket Lab Corp. engages in the development of rocket launch and control systems for the space and defense industries. It operates through the Launch Services and Space Systems segments. The Launch Services segment provides launch services to customers on a dedicated mission or ride share basis. The Space Systems segment consists of spacecraft engineering and design services, spacecraft components, spacecraft manufacturing, and on-orbit mission operations. The company is headquartered in Long Beach, CA.

Rocket Lab Corp.

Rocket Lab USA Inc

Rocket Lab is trending as investors react to recent news, including a new multi-launch agreement with Japan's iQPS. The community is actively discussing the potential impact of this deal, along with speculation about upcoming catalysts like the Neutron launch and potential government contracts. Some traders caution about short-term overvaluation, while long-term bulls remain confident in the company's growth prospects.

MARA Holdings, Inc. is a digital asset technology company, which engages in mining cryptocurrencies with a focus on the Bitcoin ecosystem. It also deals with owning and operating bitcoin mining facilities or data centers, selling proprietary software or technology to third parties operating in the Bitcoin ecosystem, offering advisory and consulting services to support Bitcoin mining ventures in domestic and international jurisdictions, and generating electricity from renewable energy resources or methane gas capture to power Bitcoin mining projects. The company was founded on February 23, 2010 and is headquartered in Hallandale Beach, FL.

MARA Holdings Inc.

Marathon Digital Holdings Inc

MARA is trending as discussions revolve around its potential to catch up with other miners like CLSK and IREN, with some expressing frustration over its underperformance and management. Community members are debating whether its current valuation reflects its Bitcoin holdings and future AI prospects. Short interest remains high, fueling speculation about a potential squeeze.

Litecoin is a peer-to-peer cryptocurrency created by Charlie Lee. It was created based on the Bitcoin protocol but differs in terms of the hashing algorithm used. Litecoin uses the memory intensive Scrypt proof of work mining algorithm. Scrypt allows consumer-grade hardware such as GPU to mine those coins.  Why Litecoin? Litecoin is a cryptocurrency that has evolved from Bitcoin after its own popularity in the industry, this alternative, or ‘altcoin’ has emerged to allow investors to diversify their digital currency package, according to Investopedia. Litecoin is one of the most prominent altcoins and was created by former Google employee and Director of Engineering at Coinbase, Charlie Lee. Litecoin was the first to alter Bitcoin and the most significant difference is that it takes 2.5 minutes for Litecoin to generate a block, or transaction, in comparison to Bitcoin's 10 minutes.  ‘While this matters little to traders, miners who use hardware to run Bitcoin's network cannot switch over to Litecoin. This keeps bigger mining conglomerates away from Litecoin because they cannot easily optimize their profits by swapping to another coin, contributing to a more decentralized experience. Litecoin also has bigger blocks, and more coins in circulation, making it more affordable and swift when transacting,’ Investopedia explained.  As explained above, Litecoin can transact a lot faster than Bitcoin, but there are also a number of other characteristics that investors need to know before trading. Litecoin can handle higher volumes of transactions because of the capability of transacting faster and if Bitcoin attempted to transact on the scale of its altcoin, a code update would be needed. However, Litecoin’s blocks would be larger, but with more ‘orphaned blocks'. The faster block time of litecoin reduces the risk of double spending attacks - this is theoretical in the case of both networks having the same hashing power.  Litecoin Technical Details: The transaction confirmation time taken for Litecoin is about 2.5 minutes on average (as compared to Bitcoin's 10 minutes). The Litecoin network is scheduled to cap at 84 million currency units.   Litecoin has inspired many other popular alternative currencies (eg. Dogecoin) because of its Scrypt hashing algorithm in order to prevent ASIC miners from mining those coins. However it is said that by the end of this year, Scrypt ASIC will enter the mass market.

Litecoin

Litecoin is surging, fueled by speculation around a potential ETF and positive technical indicators, leading to renewed interest in the crypto asset. The community is actively discussing price targets and potential breakouts, while also debating whether this rally will be sustained. Some traders are pointing to Litecoin's historical performance relative to Bitcoin, suggesting it is undervalued.

American Battery Technology Co. is a technology company, which engages in the development and marketing of lithium-ion batteries. Its projects include recycling plant, United States Advanced Battery Consortium (USABC), and Tonopah flats. The company was founded on October 6, 2011 and is headquartered in Reno, NV.

American Battery Technology Company

American Battery Technology Company ($ABAT) is trending as the stock price increases, spurring excitement among long-term investors who have been holding shares for several years and are now seeing significant gains. Community members are actively discussing potential price targets and the impact of upcoming news, particularly around the PFS (Pre-Feasibility Study). The company's positioning in lithium recycling, especially with potential government support and China's export controls, is also a key talking point.

One & One Green Technologies, Inc. engages in the recycle, production and trade of scrap metals. Its products include copper alloy ingot, aluminum scrapes, and plastic beads. The company was founded on April 17, 2024 and is headquartered in Bulacan, Philippines.

One and one Green Technologies. Inc - Ordinary Shares - Class A

Fueled by its recent IPO, $YDDL is trending due to significant after-hours volatility and a low float, leading to speculation of a potential massive run. The stock's connection to AI and green technology is adding to the excitement, though some traders express concerns about it being a pump and dump. Community members are actively discussing potential price targets and whether the stock can maintain its momentum.

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Philip Morris International Inc. (PM) said on Wednesday that its experts met with the Tobacco Products Scientific Advisory Committee on October 7 as it seeks to continue marketing versions of its IQOS heated tobacco products in the U.S. as modified risk tobacco products.The committee provides nonbinding recommendations to the U.S. Food and Drug Administration’s (FDA) Center for Tobacco Products (CTP). The modified risk tobacco product designation granted by the FDA initially in 2020 allowed the company to advertise its perks, including that the IQOS system heats tobacco instead of burning it, significantly reducing the production of and users’ exposure to harmful chemicals.PMI has requested that it be allowed to continue marketing versions of IQOS as modified risk tobacco products.“We encourage the FDA to continue efforts to establish a timely scientific review process for smoke-free products—including for IQOS ILUMA, which has been pending FDA review for nearly two years and has globally shown even higher rates of legal-age adults fully switching from combustible cigarettes—that are a better choice for legal-age adults who would otherwise use traditional tobacco products, including combustible cigarettes,” PMI U.S. CEO Stacey Kennedy <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://www.businesswire.com/news/home/20251008608945/en/Philip-Morris-International-Urges-U.S.-Food-and-Drug-Administration-Advisory-Committee-to-Recommend-Continued-Marketing-of-IQOS-as-Modified-Risk-Product">said</a>.The company estimates that there are approximately 34 million IQOS consumers globally who have moved away from cigarettes or significantly reduced their consumption as of June 30. PMI first entered the U.S. market in 2022, following its acquisition of Swedish Match.On Stocktwits, retail sentiment around PM stock fell from 'extremely bullish' to 'bullish' territory over the past 24 hours, while message volume stayed at 'high' levels.&nbsp;<a href="https://stocktwits.com/symbol/PM">PM stock</a> is up by 28% this year and by 30% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/ford-faces-1-billion-hit-after-new-york-aluminum-plant-fire-analysts-say/ch6EZaVR3iF">Ford Faces Up To $1 Billion Hit After New York Aluminum Plant Fire, Analysts Reportedly Say</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

In this photo illustration, the logo of Philip Morris International Inc. is displayed on a smartphone screen, with the company's branding in the background, on April 20, 2025, in Chongqing, China. (Photo by Cheng Xin/Getty Images)

Philip Morris Seeks FDA Approval To Keep IQOS Modified Risk Designation For Later Versions Of Device

The modified risk tobacco product designation granted by the FDA initially in 2020 allowed the company to advertise IQOS’ perks. 

Equity

Shares of CarMax (KMX) slumped 24% on Thursday morning after the company’s second-quarter earnings fell below Wall Street expectations, sparking a downgrade by Wedbush.<a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://media.carmax.com/press-releases/news-release/2025/CarMax-Reports-Second-Quarter-Fiscal-Year-2026-Results/default.aspx">Total vehicle sales</a> for the company declined 4.1% year-over-year in the quarter to 338,031 units, resulting in a 6% decrease in revenue to $6.59 billion, which fell short of the estimated $7.02 billion. Net earnings per share came in at $0.64, down from $0.85 in the corresponding quarter of 2024.Total net income declined 28% to $95.4 million, while income from the company’s auto finance business fell 11.2% to $102.6 million. The company pinned the drop in income from the auto finance segment to an increase in the provision for loan losses, which outweighed growth in net interest margin.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/KMX">KMX stock</a> stayed within ‘extremely bullish’ territory over the past 24 hours, while message volume rose from ‘high’ to ‘extremely high’ levels.CEO Bill Nash admitted that the quarter was “challenging,” but said the used auto retailer remains confident in its long-term strategy. Wedbush subsequently downgraded CarMax to ‘Neutral’ from ‘Outperform’ and revised the price target to $54, down from $84.The new price target implies a downside of about 5% from the stock’s closing price on Wednesday.The "weak results" in Q2 underperformed expectations across "all key metrics," Wedbush said. &nbsp;These results are amplifying investors' concerns around management's ability to sustain market leadership and drive additional growth, according to the analyst. Wedbush is now eyeing a potential revision of its estimates for the company following the earnings call.KMX stock is down 46% this year and approximately 41% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/pepgen-stock-more-than-doubles-on-thursday/chDla07R34F">PepGen Stock More Than Doubles On Thursday – Check Out The New Price Targets On Wall Street</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

A view of a CarMax dealership on April 10, 2025 in Santa Rosa, California. (Photo by Justin Sullivan/Getty Images)

Why Did CarMax Stock Tumble 24% Today?

Total vehicle sales of the company fell 4.1% year-over-year in the second quarter to 338,031 units, dragging revenue by 6% to $6.59 billion.

Bristol Myers Squibb (BMY) announced on Thursday that it will sell its moderate-to-severe plaque psoriasis drug, Sotyktu, at a discount of more than 80% to the current list price, starting in January 2026, to cash-paying patients.Patients can purchase the drug at a discount on the company’s BMS Patient Connect direct-to-patient platform. Eligible cash-paying U.S. patients with a Sotyktu prescription can buy the medicine through the platform, which offers shipping across all 50 states and Puerto Rico, the company <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://news.bms.com/news/corporate-financial/2025/Bristol-Myers-Squibb-Builds-on-Eliquis-apixaban-Direct-to-Patient-Program-Announces-New-BMS-Patient-Connect-Platform-Offering-Sotyktu-deucravacitinib/default.aspx">stated</a>. The platform will also provide patient support resources, it added.“We are taking a leading role in removing barriers, providing transparency and lowering out-of-pocket costs so patients in the United States can get the treatments they need – delivered directly to their door, wherever they are in the country,” CEO Christopher Boerner said.The announcement comes on the heels of President Trump <a href="https://stocktwits.com/news-articles/markets/equity/trump-to-issue-60-day-warning-letters-to-drugmakers-over-pricing/choL0IMRdGB">sending</a> letters to 17 drugmakers demanding that they lower drug prices in the U.S. to levels paid by other wealthy nations. The deadline for meeting the demand is on Monday, and the White House has warned of action against those who do not comply.Shares of the company traded 0.3% higher in the pre-market session at the time of writing. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/BMY">BMY stock</a> rose from ‘bullish’ to ‘extremely bullish’ territory over the past 24 hours, while message volume stayed at ‘high’ levels.In July, the company also <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://google.com/url?q=https://stocktwits.com/news-articles/markets/equity/bristol-myers-pfizer-to-offer-blood-thinning-drug-at-discount/ch8K8XqR5pI&amp;sa=D&amp;source=docs&amp;ust=1758807238695403&amp;usg=AOvVaw1vujNK93MaBpbwKU9R5Fiv">announced</a> that it will sell its blood thinner drug Eliquis to cash-paying patients for more than 40% discount to the current list price. Eliquis is a prescription medicine used in adults to reduce the risk of stroke and blood clots in people who have atrial fibrillation (AFib), a type of irregular heartbeat, not caused by a heart valve problem. It is also used to treat blood clots in the veins of the legs or lungs, and reduce the risk of them occurring again after receiving treatment for blood clots.BMY stock is down approximately 22% this year and by about 12% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/capricor-stock-rises-pre-market-over-fresh-hopes-of-deramiocel-approval-in-treating-genetic-disorder/chDlIyZR34h">Capricor Stock Rises Pre-Market Over Fresh Hopes of Deramiocel Approval In Treating Genetic Disorder</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

In this photo illustration, the Bristol-Myers Squibb Company logo is seen displayed on a tablet. (Photo Illustration by Igor Golovniov/SOPA Images/LightRocket via Getty Images)

Bristol Myers To Sell Plaque Psoriasis Drug For Over 80% Discount Starting In 2026

Patients can purchase the drug at a discount on the company’s BMS Patient Connect direct-to-patient platform.

Shares of DexCom (DXCM) declined 10% on Friday after investment firm Hunterbrook Capital disclosed a short position in the stock.Hunterbrook <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://hntrbrk.com/dexcom/">said</a> on Thursday that it has a short position on DXCM based on Hunterbrook Media’s reporting, which stated that after inaccurate readings from Dexcom’s flagship G7 continuous glucose monitor (CGM) device, “some diabetics are ending up in the ICU — or dead.” Hunterbrook Media is an investigative news outlet.The report stated that DexCom made an unauthorized design change to a key component of the G7 that internal studies showed was inferior by “every accuracy metric,” and the company sold the device anyway. This change was revealed during a surprise inspection by the U.S. Food and Drug Administration (FDA), the report stated.Several company executives left the company amid the FDA’s scrutiny and soaring complaints, the report said, while adding that patients are now returning to the G6 or switching to products from competitors, such as Abbott (ABT).Hunterbrook also stated that it has shared its probe with a senior official from the Health and Human Services (HHS) and requested that the FDA intervene. The firm also said that DexCom didn't respond to their requests for comments. The report named people who died or had to be hospitalized following wrong readings by the G7 device, including Billy Sosbe, who died in June, and Diana Bates Knight, who rushed her 6-year-old to the emergency, after the device misread her blood sugar by hundreds of points.“In Dexcom’s crisis, Abbott may see its chance. Our analysis of FDA data shows Dexcom receives more accuracy complaints than its market share predicts; Abbott receives significantly fewer,” Hunterbrook said.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/DXCM">DXCM</a> rose from ‘bearish’ to ‘bullish’ territory over the past 24 hours, while message volume rose from ‘normal’ to ‘high’ levels.<figure class="image"><img style="aspect-ratio:578/57;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_19_at_2_14_55_PM_png_eb2477f011.webp" alt="DXCM's Sentiment Meter and Message Volume as of 2:15 p.m. ET on Sept. 19, 2025 | Source: Stocktwits" width="578" height="57"><figcaption>DXCM's Sentiment Meter and Message Volume as of 2:15 p.m. ET on Sept. 19, 2025 | Source: Stocktwits</figcaption></figure>A Stocktwits user opined that DexCom has proven technology and is leading in CGM.<stembedurl>https://stocktwits.com/CmonManGiveMeABreak/message/629329227</stembedurl>Another user, however, opined that the FDA might pull the G7 device from the market.<stembedurl>https://stocktwits.com/buddyopalosam/message/629325830</stembedurl>DXCM stock is down by 13% this year and by 5% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/equity/markets/kalvista-pharmaceuticals-hereditary-angioedema-drug-approved-in-eu-switzerland/chD3BkIR3TW">KalVista Pharmaceuticals’ Hereditary Angioedema Drug Approved In EU, Switzerland: Retail Sees Stock Rallying To $22 In A Year</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

In this photo illustration, the DexCom logo is seen displayed on a smartphone screen. (Photo Illustration by Thomas Fuller/SOPA Images/LightRocket via Getty Images)

DexCom Stock Slumps 10% After Hunterbrook Media Investigation Raises Concerns About Its G7 Device

Hunterbrook Capital said on Thursday that it has a short position in DXCM stock based on Hunterbrook Media’s reporting, which stated that some diabetics died after inaccurate readings from Dexcom’s G7  device.

Hunterbrook Capital said on Thursday that it has a short position in DXCM stock based on Hunterbrook Media’s reporting, which stated that after inaccurate readings from Dexcom’s G7 continuous glucose monitor device, some diabetics are ending up in the ICU or dead.


Shares of GE Healthcare Technologies (GEHC) jumped 1% in the pre-market session on Thursday, following reports that the company is considering options, including the sale of a stake in its China unit.Bloomberg <a target="_blank" rel="noopener noreferrer nofollow" href="https://www.bloomberg.com/news/articles/2025-09-18/ge-healthcare-is-said-to-explore-selling-stake-in-china-business?srnd=homepage-asia">reported</a> on Thursday, citing people familiar with the matter, that the U.S.medical technology company has been working with advisers to evaluate options for the business. A potential transaction may value the China assets at several billion dollars, the report said.However, no final decision has been made on the timing and size of a potential disposal, and considerations are preliminary, sources told Bloomberg. According to the report, China is the company’s second-largest market, with approximately 7,000 employees in the region. &nbsp;On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/GEHC">GEHC stock</a> fell from ‘bullish’ to’ neutral’ territory over the past 24 hours, while message volume stayed at ‘normal’ levels.<figure class="image"><img style="aspect-ratio:928/100;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_18_083008_png_caa300d3aa.webp" alt="GEHC's Sentiment Meter and Message Volume as of 7:49 a.m. ET on Sept. 18, 2025 | Source: Stocktwits" width="928" height="100"><figcaption>GEHC's Sentiment Meter and Message Volume as of 7:49 a.m. ET on Sept. 18, 2025 | Source: Stocktwits</figcaption></figure>GE Healthcare was spun off from General Electric in 2023. It delivers advanced technologies, pharmaceutical diagnostics, and AI-powered tools for medical use. According to the company, it has over 200 imaging software applications and treats over a billion patients annually.In February, the company said that its revenue growth in the U.S. in 2024 was partially offset by continued market softness in China. For the second quarter, GE Healthcare reported adjusted earnings per share of $1.06, compared to $1 in the corresponding quarter of 2024, and revenue growth of 3% on a reported basis to $5 billion.GEHC stock is down 2% this year and approximately 13% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/why-did-89bio-stock-nearly-double-in-value/chDcHJIR3bc">Why Did 89bio Stock Nearly Double In Value Today?</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

In this photo illustration, a smartphone displays the logo of GE HealthCare Technologies Inc. in front of a screen showing the company's latest stock market chart on July 28, 2025 in Chongqing, China. (Photo illustration by Cheng Xin/Getty Images)

GE Healthcare Reportedly Eyes Selling Stake In China Unit – More Details Inside

According to a Bloomberg report, no final decision has been made on the timing and size of a potential disposal, and considerations are preliminary.

Regeneron Pharmaceuticals, Inc. (REGN) said on Monday that its experimental therapy significantly reduced symptoms of cat and birch allergies in late-stage trials, successfully meeting their key endpoints.In the <a target="_blank" rel="noopener noreferrer nofollow" href="https://investor.regeneron.com/news-releases/news-release-details/regeneron-advances-allergy-pipeline-two-positive-phase-3-trials">trials</a>, patients with moderate to severe cat or birch allergies received direct instillation of either cat dander or birch pollen into the eyes, followed by a single subcutaneous administration of the allergen-blocking antibodies. The antibody blockers “significantly reduced” allergy symptoms compared to placebo, the company said.The company stated that the data from the studies will be presented at an upcoming medical conference and used to inform confirmatory late-stage trials. Both the cat and birch allergy programs are part of a broader allergy pipeline, which includes an ongoing study in adults with severe food allergy. Initial results from the food allergy trial have been encouraging, the company said on Monday.Regeneron Chief Scientific Officer George D. Yancopoulos stated on Monday that the company anticipates significant relief at the earliest assessment time point, which is expected to last over three months, in both our cat and birch allergy programs.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/REGN">REGN stock</a> fell from ‘bullish’ to ‘neutral’ territory over the past 24 hours, while message volume stayed at ‘low’ levels. Shares of the company traded 1% higher in the pre-market session at the time of writing.Yancopoulos said that while millions suffer from the effects of allergies, most undergo allergy desensitization shots, often with disappointing results.“The purpose of these burdensome allergy shots is to try to build up allergen-blocking antibodies in the body. We wondered whether we could instead manufacture and directly provide allergen-blocking antibodies,” he said. “These recent Phase 3 allergen challenge trials, together with our earlier Phase 2 trials, provide compelling evidence that our first-in-class approach can have the potential to provide profound allergy relief – rapidly and durably after a single treatment – decreasing ocular, nasal and even asthma measures.”Regeneron noted that Birch pollen is one of the most common seasonal allergens in the U.S., affecting more than 10 million people, while cat allergy affects more than 20 million people. In the trials, patients received a combination of two antibody blockers or a placebo. Those who received the combination had fewer allergy symptoms, such as conjunctival redness.While additional late-stage trials in cat allergy are planned to begin in the first half of 2026, further late-stage development in birch allergy is expected to commence by the end of the year.REGN stock is down by 20% this year and by about 50% over the past 12 months.Read also: <a href="https://stocktwits.com/news-articles/markets/equity/echostar-to-dell-17-billion-in-spectrum-assets-to-spacex/chwWH3JRdAD">EchoStar To Sell $17B In Spectrum Assets To SpaceX – Stock Rockets 40% Pre-Market</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.Get updates to this developing story <a href="https://stocktwits.com/news-articles/markets/equity/regeneron-says-experimental-therapy-reduced-symptoms-of-cat-birch-allergies-in-studies/chwWH37RdAw">directly on Stocktwits.</a>

In this photo illustration, the Regeneron Pharmaceuticals company logo is displayed on a smartphone screen. (Photo Illustration by Piotr Swat/SOPA Images/LightRocket via Getty Images)

Regeneron Says Experimental Therapy Reduced Symptoms Of Cat, Birch Allergies In Late-Stage Trials

The company said that the antibody blockers “significantly reduced” allergy symptoms compared to a placebo in the trials. 

Regeneron Pharmaceuticals, Inc. (REGN) announced on Tuesday that the late-stage trial evaluating its investigational Cemdisiran monotherapy in adults with generalized myasthenia gravis (MG) yielded positive results.MG is a rare and chronic autoimmune disease where disrupted communication between nerves and muscles results in debilitating and potentially life-threatening muscle weakness. According to Regeneron, the disease impacts approximately 85,000 people in the U.S.Both Cemdisiran and the combination of Cemdisiran and the approved antibody Pozelimab (cemdi-poze) demonstrated improvements in activities of daily functioning such as talking, eating, breathing, vision, and mobility at week 24. Cemdisiran showed numerically better results across all generalized myasthenia gravis-specific outcomes, the company <a target="_blank" rel="noopener noreferrer nofollow" href="https://newsroom.regeneron.com/news-releases/news-release-details/regeneron-announces-positive-results-phase-3-trial-generalized">said</a>.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/REGN">REGN stock</a> jumped from ‘bullish’ to ‘extremely bullish’ territory over the past 24 hours, while message volume stayed at ‘high’ levels. Shares of the company traded 2% higher at the time of writing.<figure class="image"><img style="aspect-ratio:576/61;" src="https://news.stocktwits-cdn.com/Screenshot_2025_08_26_at_12_07_06_PM_png_ed2effdb15.webp" alt="REGN's Sentiment Meter and Message Volume as of 12:07 p.m. ET on Aug. 26, 2025 | Source: Stocktwits" width="576" height="61"><figcaption>REGN's Sentiment Meter and Message Volume as of 12:07 p.m. ET on Aug. 26, 2025 | Source: Stocktwits</figcaption></figure> A Stocktwits user believes that the stock may hit an all-time low soon.<stembedurl>https://stocktwits.com/Johny34211/message/626531477</stembedurl>The firm said that treatment-emergent adverse events (TEAEs) occurred in 69% of patients treated with Cemdisiran, 81% with cemdi-poze, and 77% with placebo. Serious TEAEs occurred in 3% of patients treated with Cemdisiran, 9% with cemdi-poze, and 14% with placebo, the company said. However, there were no treatment discontinuations due to adverse events through week 24 in the Cemdisiran arm, it added.The company also said that there were no deaths during the 24-week placebo-controlled portion of the trial. During the extension period, however, one death due to pneumonia occurred in the Cemdisiran arm, and one death due to septic shock occurred in the combination arm. Both deaths occurred in patients who were on concomitant immunosuppressive therapies, Regeneron said.The company now plans to apply for regulatory approval in the U.S. for Cemdisiran in the first quarter of 2026, pending discussions with the U.S. Food and Drug Administration (FDA).REGN stock is down by 18% this year and by 51% over the past 12 months.&nbsp;Also See: <a href="https://stocktwits.com/news-articles/markets/equity/jpmorgan-upgraded-nio-shares-with-price-target-hike/chsHCIGRdjA">This Chinese EV Stock Surged 8% Today And JPMorgan Just Upgraded The Shares With A Price Target Hike: Retail Eyes $10 By End Of Week</a>For updates and corrections, email newsroom[at]stocktwits[dot]com

Regeneron Stock Rallies After Therapy For Autoimmune Disease Meets Late-Stage Trial Goals: Retail Thinks Stock Might Hit An All-Time Low Soon

The company now plans to apply for regulatory approval in the U.S. for Cemdisiran in the first quarter of 2026, pending discussions with the FDA.

Regeneron Pharmaceuticals, Inc. (REGN) announced on Wednesday that the U.S. Food and Drug Administration (FDA) has extended the date by which it is expected to rule on two of its EYLEA HD Injection regulatory submissions.The company <a target="_blank" rel="noopener noreferrer nofollow" href="https://newsroom.regeneron.com/news-releases/news-release-details/eylea-hdr-aflibercept-injection-8-mg-applications-expanded-us">said</a> that the FDA will now decide on its submissions by the fourth quarter of 2025. The agency extended review time after determining that information provided since the completion of a recent inspection of a third-party manufacturer constituted a major amendment to each submission. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/REGN">REGN</a> remained within the ‘bullish’ territory over the past 24 hours, while message volume increased from ‘low’ to ‘normal’ levels.Regeneron had submitted applications pertaining to the EYLEA HD prefilled syringe and another seeking approval for both the treatment of macular edema following retinal vein occlusion (RVO) and the broadening of the dosing schedule to include every 4-week dosing across approved indications. The delay, however, was <a href="https://stocktwits.com/news-articles/markets/equity/truist-cuts-price-target-on-regeneron-citing-near-term-investor-focus-on-eylea/chrHEcxRdeF">anticipated</a>, the company said.The firm said it resulted from observations during an FDA general site inspection at Catalent Indiana LLC, &nbsp;the filler for these regulatory applications.Novo Nordisk recently acquired Catalent. The firm submitted a response earlier this month to address the observations noted by the FDA. Regeneron said that the FDA will be able to act on its applications once the manufacturing issues are resolved. The FDA was previously expected to decide on the submissions by August 2025.EYLEA HD, however, remains available in the U.S. through vial administration and is approved to treat vision-threatening conditions that impact patients, such as wet age-related macular degeneration (wAMD), diabetic macular edema (DME), and diabetic retinopathy (DR).REGN stock is down by 17% this year and by about 51% over the past 12 months.&nbsp;Read also: <a href="https://stocktwits.com/news-articles/markets/equity/elon-musk-says-tesla-model-yl-might-not-ever-come-to-us-markets/chsitLlRdhq">Elon Musk Said Tesla’s Model Y L Might Not Ever Come To US Markets – Here’s Why</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

Regeneron Says FDA Will Take More Time to Review Its Two Eylea HD Submissions

The company said that the FDA will now decide on its submissions by the fourth quarter of 2025.

Humana Inc. (HUM) on Tuesday announced measures aimed at accelerating prior authorizations for care services, particularly outpatient services such as colonoscopies and CT scans.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/HUM">Humana</a> trended within ‘bullish’ territory, accompanied by ‘high’ message volume.<figure class="image"><img style="aspect-ratio:624/64;" src="https://news.stocktwits-cdn.com/Screenshot_2025_07_22_at_9_02_08_AM_png_e240f6341d.webp" alt="HUM's Sentiment Meter and Message Volume as of 9 a.m. ET on July 22, 2025 | Source: Stocktwits" width="624" height="64"><figcaption>HUM's Sentiment Meter and Message Volume as of 9 a.m. ET on July 22, 2025 | Source: Stocktwits</figcaption></figure>The actions, the health insurance company said, will reduce the number of prior authorization requirements and make the process faster and more seamless while preserving the system of checks and balances that ensures the most high-cost, high-risk treatments are reviewed and approved before care is delivered.Humana CEO Jim Rechtin said that the current healthcare system is “too complex, frustrating, and difficult to navigate,” while emphasising the need to “do better.”“We are committed to reducing prior authorization requirements and making this process faster and more seamless to better support patients, caregivers, physicians, and healthcare organizations,” he added.By the start of 2026, Humana will eliminate approximately one-third of prior authorizations for outpatient services and provide a decision within one business day on at least 95% of all complete electronic prior authorization requests. Currently, Humana provides a decision within one business day on more than 85% of outpatient procedures.Humana will remove the authorization requirement for diagnostic services, including colonoscopies and transthoracic echocardiograms, as well as select CT scans and MRIs, by January 1, it said. &nbsp;The company also announced that it will launch a new gold card program in 2026, which will waive prior authorization requirements for certain items and services for providers who have a proven record of submitting coverage requests that meet medical criteria.Starting in 2026, the insurance provider will also report its prior authorization metrics to increase transparency. This includes prior authorization requests that are approved, denied, and approved after appeal, as well as the average time between submission and decision.A Stocktwits user opined that while Humana stock has fallen as hard as its peer, UnitedHealth, it does not share the same stigma as UNH.<stembedurl>https://stocktwits.com/Chartist0_0/message/621888373</stembedurl>However, it is essential to note that UNH shares have dropped 44% this year.Meanwhile, HUM stock is down 10% this year and approximately 41% over the past 12 months.Read Next: <a href="https://stocktwits.com/news-articles/markets/equity/gm-mary-barra-highlights-efforts-to-mitigate-tariff-impact-in-future-after-q2-earnings-take-hit/ch8M15MR5tG">GM’s Mary Barra Highlights Efforts To Mitigate Tariff Impact After Q2 Earnings Take Hit: Retail Sees Levies Impact Consumer Spending</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

The MyHumana app page is displayed on a smartphone in the Apple App Store in front of the Humana Inc logo on October 30, 2024 in Chongqing, China. (Photo by Cheng Xin/Getty Images)

Humana To Slash Red Tape Around Prior Authorization For Care Services By 2026: Retail Remains Optimistic

Humana CEO Jim Rechtin said that the current healthcare system is “too complex, frustrating, and difficult to navigate” while emphasising the need to “do better.”

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