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Navitas Semiconductor Corp. engages in the development of ultra-efficient gallium nitride (GaN) semiconductors. Its GaN power ICs integrate GaN power with drive, control and protection to enable charging, power density, and energy savings for mobile, consumer, enterprise, eMobility and new energy markets. The company was founded by Daniel Kinzer, Nick Fichtenbaum, Gene Sheridan, and Jason Zhang on August 12, 2020 and is headquartered in Torrance, CA.

Navitas Semiconductor Corp

NVTS is trending following news of its progress supporting NVIDIA's next-generation AI factory computing platforms, specifically focused on 800V power architecture. The community is discussing the potential for a short squeeze and the company's role in AI infrastructure, with some drawing comparisons to other high-flying stocks. Bullish sentiment is fueled by the potential for increased efficiency and reduced energy consumption in AI data centers.

Novavax, Inc. Is a biotechnology company, which engages in the discovery, development, and commercialization of recombinant vaccines. The company was founded in 1987 and is headquartered in Gaithersburg, MD.

Novavax, Inc.

Novavax Inc

Novavax is trending as investors discuss Shah Capital's push for the company's sale to a larger pharmaceutical entity to unlock shareholder value. The community is debating the potential buyout price, partnership opportunities, and the company's future prospects under new ownership. Some are frustrated with current management, while others remain optimistic about Novavax's fundamentals and technology.

Greenwave Technology Solutions, Inc. is an emerging growth company, which engages in recycling ferrous metal. It also recycles nonferrous metals including aluminum, copper, stainless steel, nickel, brass, titanium, lead, alloys, and mixed metal products. The company was founded on April 26, 2013 and is headquartered in Chesapeake, VA.

Greenwave Technology Solutions Inc

GWAV is trending due to a planned reverse stock split, which is sparking discussions about potential short squeezes and future price movements. While some traders are optimistic about quick gains, others express concern over the company's history of reverse splits and potential dilution. The community is actively debating the stock's short-term potential versus long-term risks.

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 ($LAES) is trending following news of a strategic collaboration with Wecan Group to develop a post-quantum KYC solution, positioning the company as a key player in cybersecurity. The community is buzzing about the potential for a gamma squeeze due to options expiring soon, with some anticipating a significant rise towards double digits. Small cap investors are particularly excited about the upside potential of this stock in the quantum technology and AI revolution.

Nova Minerals Ltd. engages in the exploration and development of mineral properties. Its projects include Estelle Gold, RPM, Korbel, Train, Stoney and Studies projects. The company was founded in January 1987 and is headquartered in Melbourne, Australia.

Nova Minerals Limited - ADR

Nova Minerals is trending due to positive updates on their Alaskan gold and antimony project, including high-grade gold assay results and news of extinguished debt, sparking investor interest. The community is discussing the company's potential to benefit from increased antimony prices and its undervalued status compared to peers. There is also speculation about the company receiving government grants to develop a domestic antimony supply chain.

BioCryst Pharmaceuticals, Inc. is a biotechnology company. It engages in the provision of structure-guided drug design with the goal of developing oral small-molecule and protein therapeutics to target difficult-to-treat rare diseases. The company was founded by William M. Spencer III, Charles E. Bugg, and John A. Montgomery in 1986 and is headquartered in Durham, NC.

Biocryst Pharmaceuticals Inc.

Biocryst is trending as investors discuss the company's acquisition of Astria Therapeutics for $700M, a move aimed at bolstering their HAE portfolio with a late-stage, long-acting plasma kallikrein inhibitor; navenibart. Community chatter revolves around the deal's financial implications, potential dilution, and the strategic shift from in-house development to acquisitions, with some expressing concerns over increased debt and the timeline for potential returns while others are optimistic about the company's strengthened position in the HAE market.

Critical Metals Corp. engages in the mining, exploration, and development of lithium metals. It owns Wolfsberg Project and Tanbreez Project. The company was founded on October 24, 2022 and is headquartered in British Virgin Islands.

Critical Metals Corp.

Critical Metals Corp. is trending due to increasing investor excitement surrounding rare earth mineral stocks and the potential for U.S. government funding to boost domestic supply. Community members are discussing the stock's potential for significant gains amidst rising U.S.-China trade tensions and growing recognition of rare earth elements as vital for national security.

American Resources Corp. engages in the extraction, processing, transportation, and distribution of metallurgical coal to the steel industry. It focuses on the operation of coal mining complexes located primarily within Pike, Knott, and Letcher Counties, Kentucky, and Wyoming County, West Virginia. The company was founded in 2006 and in headquartered in Fishers, IN.

American Resources Corporation - Ordinary Shares - Class A

American Resources Corporation ($AREC) is trending due to ongoing discussions around rare earth elements and critical minerals, particularly following news of a $33M financing deal. The community is debating the implications of potential dilution versus the benefits of increased capital for expansion, especially regarding ReElement Technologies and government interest. Some investors express concerns about past performance and management, while others are optimistic about the company's role in the domestic rare earth supply chain and potential for a ReElement IPO.

Candel Therapeutics, Inc. is a clinical stage biotechnology company, which engages in the development and commercialization of viral immunotherapies. Its pipeline includes CAN-2409 and CAN-3110. The company was founded by Estuardo Aguilar-Cordova in 2002 and is headquartered in Needham, MA.

Candel Therapeutics Inc

Candel Therapeutics ($CADL) is trending due to positive community sentiment surrounding a recent $130M term loan, viewed as a strategic move to independently advance their lead lung cancer treatment and bypass potential dilution. Investors are actively discussing the implications for future partnerships or a buyout, with many believing the company is positioned for long-term growth and value creation. Community members are also focused on upcoming data releases, particularly related to CAN-3110, and speculating on potential partnership announcements.

Bitcoin is the first successful internet money based on peer-to-peer technology; whereby no central bank or authority is involved in the transaction and production of the Bitcoin currency. It was created by an anonymous individual/group under the name, Satoshi Nakamoto. The source code is available publicly as an open source project, anybody can look at it and be part of the developmental process.  Bitcoin is changing the way we see money as we speak. The idea was to produce a means of exchange, independent of any central authority, that could be transferred electronically in a secure, verifiable and immutable way. It is a decentralized peer-to-peer internet currency making mobile payment easy, very low transaction fees, protects your identity, and it works anywhere all the time with no central authority and banks.  Bitcoin is designed to have only 21 million BTC ever created, thus making it a deflationary currency. Bitcoin uses the SHA-256 hashing algorithm with an average transaction confirmation time of 10 minutes. Miners today are mining Bitcoin using ASIC chip dedicated to only mining Bitcoin, and the hash rate has shot up to peta hashes.  Being the first successful online cryptography currency, Bitcoin has inspired other alternative currencies such as Litecoin, Peercoin, Primecoin, and so on.  The cryptocurrency then took off with the innovation of the turing-complete smart contract by Ethereum which led to the development of other amazing projects such as EOS, Tron, and even crypto-collectibles such as CryptoKitties.

Bitcoin

Bitcoin is trending as the community debates its recent price volatility and potential support levels, with some anticipating a drop below $100K while others foresee a sharp reversal and new highs. Discussions also involve the impact of potential trade wars and broader macroeconomic factors on BTC's price action. Some traders point to technical indicators and whale activity as drivers of current market movements.

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Reliance Industries Ltd.

Zomato Ltd.

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HDFC Bank Ltd.

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Roche (RHHBY) on Monday stated that the U.S. Food and Drug Administration has approved the Elecsys pTau181 test developed in collaboration with Eli Lilly and Co. (LLY) for the detection of Alzheimer's disease.The blood-based test is aimed at aiding the initial assessment for Alzheimer’s disease and other causes of cognitive decline in the primary-care setting in patients aged 55 and older presenting with signs, symptoms, or complaints of cognitive decline. It measures the phosphorylated Tau (pTau) 181 protein in human plasma."By bringing Alzheimer's blood-based biomarker testing into primary care, we can help patients and their clinicians get answers sooner to support them earlier in their journeys," said Brad Moore, President and CEO of Roche Diagnostics North America.Roche also noted that Alzheimer’s biomarker testing has largely been limited to specialty settings, such as neurology.The performance of the test was evaluated in a clinical study with 312 participants. The results showed that in an early disease-stage, low-prevalence population reflective of a primary-care setting, Elecsys pTau181 could rule out Alzheimer’s pathology with a 97.9% negative predictive value. A high NPV indicates that a negative test result is a reliable indicator of not having the condition, minimizing the risk of a false negative result.Roche also recently received CE Mark certification in Europe for the Elecsys pTau181 test.&nbsp;On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/RHHBY">RHHBY</a> and <a href="https://stocktwits.com/symbol/LLY">LLY stock</a> trended in the ‘bearish’ territory over the past 24 hours with ‘low’ message volume.&nbsp;RHHBY stock is up by about 30% this year, while LLY gained 7%.For updates and corrections, email newsroom[at]stocktwits[dot]com.Also See: <a href="https://stocktwits.com/news-articles/markets/equity/keurig-dr-pepper-shares-climb-after-starboard-reportedly-takes-stake/ch6SqKAR3lE">Keurig Dr Pepper Shares Climb After Starboard Reportedly Takes Stake Amid $18B JDE Peet’s Deal</a>

A sign with the company logo sits outside of the headquarters campus of Eli Lilly and Company on March 17, 2024 in Indianapolis, Indiana. (Photo by Scott Olson/Getty Images)

FDA Approves Alzheimer’s Test Developed By Roche In Collaboration With Eli Lilly

The blood-based test is aimed at aiding the initial assessment for Alzheimer’s disease and other causes of cognitive decline in the primary-care setting in patients aged 55 and older.

Equity

Apollo Global Management (APO) is reportedly looking towards Spain as an investment opportunity, primarily in the energy transition, data center, and infrastructure development sectors.According to a Bloomberg report, Apollo’s senior advisor for Iberia, Konstantin Sajonia-Coburgo said at the media house’s Future of Finance conference in Madrid that these sectors are where Apollo will be looking for players with the “biggest needs.”Shares of <a href="https://stocktwits.com/symbol/APO">Apollo Global</a> were up marginally during premarket trading on Wednesday. Retail sentiment around the company remained unchanged in the ‘bullish’ territory compared to a day ago, with message volumes at ‘normal’ levels, according to Stocktwits data.“In Spain, the stock market only represents 10% of gross domestic product, so private investment opens a door for clients to access the other 90%” Sajonia-Coburgo said at the conference, according to the report. He noted that the economic fundamentals in Spain are currently good.“It’s going to be an approach based also on the major corporations and where we look very carefully from the credit perspective to those players with the biggest needs, so everything, which is infrastructure, energy transition, data centers,” he said.According to Bloomberg, in Spain, Apollo has signed a loan to support Neinor Homes SA’s acquisition bid for competitor Aedas Homes SA. Additionally, Apollo is also in talks to purchase a majority stake in the Spanish football club Atlético de Madrid.Shares of Apollo have declined nearly 24% this year and lost about 9% in the last 12 months.&nbsp;For updates and corrections, email newsroom[at]stocktwits[dot]com.Also See: <a href="https://stocktwits.com/news-articles/markets/equity/mccormick-sees-price-target-cuts-amid-margin-pressure-from-trump-tariffs/ch6ESIiR3iQ">McCormick Sees Price Target Cuts Amid Margin Pressure From Trump Tariffs</a>

 In this photo illustration, the Apollo Global Management company logo is seen displayed on a smartphone screen.

Apollo Global Eyes Spanish Market With Focus On Energy, Data Centers, And Infrastructure: Report

According to a Bloomberg News report, these sectors are where Apollo will be looking for players with the “biggest needs.”

H.C. Wainwright raised its price target on AnaptysBio (ANAB) to $59 from $38 on Tuesday, following the company's announcement of its plan to split its business into two.The analyst kept a ‘Buy’ rating on the shares. The new price target implies a potential upside of about 154% to the stock’s closing price on Monday.AnaptysBio <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://ir.anaptysbio.com/news-releases/news-release-details/anaptys-announces-intent-separate-biopharma-operations">stated </a>on Tuesday that its board of directors approved plans to explore separating its business into two independent, publicly traded companies. Upon completion of the split, the royalty management company will manage royalties and milestone payments from financial collaborations, including Jemperli with GSK and Imsidolimab with Vanda, with a focus on protecting and returning their value, the company said.The royalty management company is expected to require minimal infrastructure and staff, and will operate under a new name, it added.Meanwhile, the other company, referred to as Biopharma Co., will focus on biopharmaceutical operations, including the development and potential commercialization of innovative immunology therapeutics for autoimmune and inflammatory diseases, such as Rosnilimab, ANB033, and ANB101. After the split, Biopharma Co. will launch with adequate capital to fund operations for at least two years and will also operate under a new name, the company stated.The separation is expected to be completed by the end of 2026. Anaptys CEO Daniel Faga is expected to continue as CEO of the biopharma company.Shares of the company traded 30% higher on Tuesday afternoon at the time of writing. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/ANAB">ANAB stock</a> rose from ‘bullish’ to ‘extremely bullish territory’ over the past 24 hours, while message volume increased from ‘normal’ to ‘extremely high’ levels.<figure class="image"><img style="aspect-ratio:576/60;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_30_at_12_21_38_PM_png_239792a64d.webp" alt="ANAB's Sentiment Meter and Message Volume as of 12:21 p.m. ET on Sept. 30, 2025 | Source: Stocktwits" width="576" height="60"><figcaption>ANAB's Sentiment Meter and Message Volume as of 12:21 p.m. ET on Sept. 30, 2025 | Source: Stocktwits</figcaption></figure>A Stocktwits user said that they now expect the stock to crater.<stembedurl>https://stocktwits.com/CommercialREbroker/message/630482537</stembedurl>ANAB stock has more than doubled this year but dropped nearly 10% over the past 12 months.Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/novavax-amends-deal-with-sanofi-broadens-partnership/chDDB6dR3BH">Novavax Amends Deal With Sanofi, Broadens Partnership</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

In this photo illustration an AnaptysBio logo is displayed on a smartphone screen in Athens, Greece on January 13, 2023. (Photo illustration by Nikolas Kokovlis/NurPhoto via Getty Images)

AnaptysBio Stock Gets A Price Target Hike After Announcing Plan To Separate Royalty, Biopharma Businesses – Check Out The New Level

H.C. Wainwright’s new price target of $59 implies a potential upside of about 154% to the stock’s closing price on Monday. 

Eli Lilly &amp; Co. (LLY) has halted a study of its drug Bimagrumab, alone or in combination with its approved weight-loss drug Tirzepatide, in patients with obesity.A U.S. registry of clinical trials <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://clinicaltrials.gov/study/NCT06901349">indicates</a> that the study has been terminated due to strategic business reasons without elaboration.The purpose of the study was to see how well and how safely Bimagrumab, Tirzepatide, and the combination worked in lowering body weight in participants with obesity or overweight and type 2 diabetes. Tirzepatide is the active ingredient in the company’s popular obesity drug Zepbound. While the primary goal of the study was weight loss, the company also sought to identify the change in body fat mass associated with the drug.Bloomberg <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://www.bloomberg.com/news/articles/2025-09-25/lilly-halts-diabetes-trial-of-muscle-sparing-drug-with-zepbound">first</a> reported the termination of the trial. Following the development, the stock traded nearly 1% lower in Thursday’s pre-market session.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/LLY">LLY stock</a> rose from ‘extremely bearish’ to ‘bearish’ territory over the past 24 hours, while message volume stayed at ‘low’ levels.Lilly closed the mid-stage trial on June 10, after starting it in May, according to the registry. The study had 50 locations in the U.S. and abroad and was supposed to last about 13 months. Lilly gained access to Bimagrumab through its $1.925 billion acquisition of privately held Versanis Bio, which was completed in August 2023.A parallel study in obese patients without diabetes remains active, Bloomberg noted.Eli Lilly <a href="https://stocktwits.com/news-articles/markets/equity/eli-lilly-s-newest-obesity-drug-candidate-stirs-wall-street-buzz-but-not-everyone-s-sold/chmJdk1RR3q">said</a> in June that patients who took the highest dose of Bimagrumab alongside rival Novo Nordisk’s Semaglutide lost more fat mass than those on Semaglutide alone in a trial.LLY stock is down 4% this year and approximately 20% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/evaxion-stock-makes-whopping-jump-pre-market-after-outlicensing-vaccine-candidate/chDl7l1R34i">Evaxion Stock Jumps A Whopping 43% Pre-Market – Here’s What Happened</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

Eli Lilly Terminates A Study Of Bimagrumab In Obesity

A U.S. registry of clinical trials shows that the study has been terminated for strategic business reasons.

Eli Lilly and Company (LLY) announced on Tuesday that it plans to construct a new $ 6.5 billion manufacturing facility in Texas as part of its efforts to expand domestic medicine production.The new facility, located at Generation Park in Houston, marks the second of four new U.S. sites that Lilly intends to announce this year.The company <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://www.prnewswire.com/news-releases/lilly-plans-to-build-a-new-6-5-billion-facility-to-manufacture-active-pharmaceutical-ingredients-in-texas-302563621.html">stated</a> that the Houston facility will be operational within five years and will focus on manufacturing the company's pipeline of small molecule medicines across various therapeutic areas, including cardiometabolic health, oncology, immunology, and neuroscience. The company also said that the site will be among those that manufacture its much-awaited oral obesity drug Orforglipron. Lilly expects to make regulatory submissions for Orforglipron in the treatment of obesity by the end of this year."Our new Houston site will enhance Lilly's ability to manufacture Orforglipron at scale and, if approved, help fulfill the medicine's potential as a metabolic health treatment for tens of millions of people worldwide who prefer the ease of a pill that can be taken without food and water restrictions," said CEO David A Ricks.According to Lilly, the new facility will bring 615 new high-wage jobs to the Greater Houston area, including engineers, scientists, and lab technicians, in addition to 4,000 construction jobs. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/LLY">LLY stock</a> stayed within ‘bearish’ territory while message volume fell from ‘normal’ to ‘low’ levels.In February, Lilly announced its plans to bolster its domestic medicine production by building four new pharmaceutical manufacturing sites in the U.S., bringing the company’s total U.S. capital expansion commitments to more than $50 billion since 2020.While three of the facilities will focus on manufacturing active pharmaceutical ingredients, reshoring critical capabilities of small molecule chemical synthesis, and further strengthening Lilly's supply chain, the fourth will extend the company's global parenteral manufacturing network for future injectable therapies, the company had said.Last week, the company also <a href="https://stocktwits.com/news-articles/markets/equity/eli-lilly-to-set-up-5-billion-facility-in-virginia/chwymFcRdzj">announced</a> plans for a $5 billion manufacturing facility in Virginia.LLY stock is down 3% this year and approximately 19% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/ionis-pharma-stock-rises-after-multiple-price-target-hikes/chDLGmZR35v">Ionis Pharma Stock Rises After Multiple Price Target Hikes On Heels Of Positive Study Results In Alexander Disease</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

Eli Lilly Announces Plan To Construct New $6.5B Facility In Texas

The new facility, located at Generation Park in Houston, marks the second of four new U.S. sites that Lilly intends to announce this year.

Shares of Scholar Rock (SRRK) rose about 2% on Tuesday morning after falling 12% in the pre-market session after the U.S. Food and Drug Administration refused to approve its Apitegromab drug for the treatment of patients with spinal muscular atrophy (SMA).The company <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://investors.scholarrock.com/news-releases/news-release-details/fda-issues-complete-response-letter-crl-apitegromab-treatment">stated</a> that the FDA raised concerns identified during a routine general site inspection of Catalent Indiana LLC, a third-party fill-finish facility. The agency did not make any observations specific to its drug or cite any other approvability concerns, including any pertaining to Apitegromab’s efficacy and safety data, the company said.Catalent Indiana was acquired by Danish drugmaker Novo Nordisk (NVO) in December. The facility submitted a response in early August 2025 to address the observations noted by the FDA and has continued to take corrective actions, the company said.Scholar Rock said it will resubmit its application for Apitegromab once Catalent Indiana’s issues with the FDA are resolved. The company stated that it believes the FDA will be able to act expeditiously on the application once the manufacturing issues have been resolved. “We are continuing to work closely with Catalent Indiana on the FDA’s manufacturing observations so that we can resubmit the apitegromab BLA (application) as soon as possible,” said CEO David L Hallal.Scholar Rock has also submitted Apitegromab for approval by the European Medicines Agency, and a decision is anticipated near mid-2026, the company said. It expects a European launch for the drug in the second half of 2026, starting with Germany.Scholar Rock believes Apitegromab may lead to a clinically meaningful improvement in motor function in patients with Spinal Muscular Atrophy (SMA), a rare, severe, genetic neuromuscular disease characterized by motor function decline.On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/SRRK">SRRK stock</a> jumped from ‘bullish’ to ‘extremely bullish’ territory over the past 24 hours, while message volume stayed at ‘extremely high’ levels.<figure class="image"><img style="aspect-ratio:576/60;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_23_at_9_42_28_AM_png_308ee0f990.webp" alt="SRRK's Sentiment Meter and Message Volume as of 9:42 a.m. ET on Sept. 23, 2025 | Source: Stocktwits" width="576" height="60"><figcaption>SRRK's Sentiment Meter and Message Volume as of 9:42 a.m. ET on Sept. 23, 2025 | Source: Stocktwits</figcaption></figure>Scholar Rock is not the only company whose submissions have been delayed or denied following the FDA’s site inspection at Catalent's Indiana facility. Last month, Regeneron (REGN) <a href="https://stocktwits.com/news-articles/markets/equity/regeneron-says-fda-will-take-more-time-to-review-its-two-eylea-hd-submissions/chsitx3Rdht">announced</a> that the FDA had extended the date by which it is expected to rule on two of its EYLEA HD Injection regulatory submissions due to issues identified at the facility. &nbsp;SRRK stock is down 23% this year but up approximately 282% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/amneal-pharma-stock-rises-on-fda-approval-for-generic-version-of-abbvie-eyedrops/chDhHHIR35Q">Amneal Pharma Stock Rises On FDA Approval For Generic Version Of AbbVie’s Eyedrops</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

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

Scholar Rock In Spotlight After FDA Refuses To Approve Muscular Atrophy Treatment Over Third-Party Manufacturing Facility Issues

The company stated that the FDA did not make any observations specific to the drug or cite any other approvability concerns, including any pertaining to Apitegromab’s efficacy and safety data. 

KalVista Pharmaceuticals (KALV) announced on Friday that the European Commission (EC) and the Swiss Agency for Therapeutic Products, Swissmedic, have approved its Ekterly for the symptomatic treatment of acute attacks of hereditary angioedema (HAE).Ekterly was approved by both agencies for the treatment of adults and adolescents aged 12 years and older with HAE. It is the first and only oral on-demand treatment for HAE in the two regions, the company <a class="st-link-external" target="_blank" rel="noopener noreferrer nofollow" href="https://ir.kalvista.com/news-releases/news-release-details/kalvista-pharmaceuticals-announces-european-commission-and">said</a>.Shares of the company traded lower by 2% at the time of writing. On Stocktwits, retail sentiment around <a href="https://stocktwits.com/symbol/KALV">KalVista</a> stayed within ‘bullish’ territory over the past 24 hours, while message volume stayed within ‘normal’ levels.<figure class="image"><img style="aspect-ratio:573/62;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_19_at_12_33_07_PM_png_055493ce17.webp" alt="KALV's Sentiment Meter and Message Volume as of 12:33 p.m. ET on Sept. 19, 2025 | Source: Stocktwits" width="573" height="62"><figcaption>KALV's Sentiment Meter and Message Volume as of 12:33 p.m. ET on Sept. 19, 2025 | Source: Stocktwits</figcaption></figure>A Stocktwits user sees the stock rallying to $22 in 12 months.<stembedurl>https://stocktwits.com/PokerMunkee/message/629305223</stembedurl>Another opined that the stock has a lot of “potential and great setup.”<stembedurl>https://stocktwits.com/Shakattack31/message/629258146</stembedurl>“With our U.S. launch progressing well and approvals now secured in the U.K., EU, and Switzerland, we look forward to bringing this innovation to more people living with HAE, beginning with our first European launch in Germany,” CEO Ben Palleiko said. The company expects to launch Ekterly in Germany in the fourth quarter and in Switzerland in the second half of 2026.The recent approvals are based on the results of a late-stage trial where Ekterly achieved significantly faster symptom relief, reduction in attack severity, and attack resolution than placebo. The results also showed that the drug was well-tolerated, with a safety profile similar to that of the placebo.The EC approval applies to all 27 EU member states as well as Iceland, Liechtenstein, and Norway. In August, the European Medicines Agency also granted Ekterly 10 years of market exclusivity.Hereditary angioedema (HAE) is a rare genetic disease caused by a deficiency or dysfunction of a protein called the C1 esterase inhibitor, where patients experience painful and debilitating attacks of tissue swelling in various locations of the body that can be life-threatening depending on the area affected. Ekterly <a href="https://stocktwits.com/news-articles/markets/equity/kalvista-gets-fda-approval-for-drug-in-treating-swelling-disorder/chFtmFCR57B">received</a> approval from the U.S. Food and Drug Administration for the treatment of HAE in July.KALV stock is up by about 61% this year and by about 24% over the past 12 months.Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/emergent-biosolutions-stock-rises-after-receiving-fresh-international-purchase-orders/chD3729R3Tf">Emergent BioSolutions Stock Rises After Receiving Fresh International Purchase Orders: Retail Says Stock Is ‘Significantly Undervalued’</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

Global stock market chart and trading board - stock photo

KalVista Pharmaceuticals’ Hereditary Angioedema Drug Approved In EU, Switzerland: Retail Sees Stock Rallying To $22 In A Year

Ekterly is now the first and only oral on-demand treatment for hereditary angioedema in the two regions, the company said. 

Ride-hailing platform Uber Technologies (UBER) announced on Thursday that it has entered into a strategic partnership with drone delivery provider Flytrex Inc.Drone delivery services are expected to begin with Uber Eats pilot markets in the U.S. by the end of the year, the company <a target="_blank" rel="noopener noreferrer nofollow" href="https://investor.uber.com/news-events/news/press-release-details/2025/Uber-Partners-with-Flytrex-to-Launch-Drone-Delivery/default.aspx">said</a>. The partnership is part of the company’s efforts to build a delivery network that extends beyond traditional modes of transport, such as cars and bikes. The company already has sidewalk robots in its network and is seeking to expand its network further with autonomous aerial delivery.<a href="https://stocktwits.com/symbol/UBER">Shares of Uber</a> traded 2% higher at the time of writing. On Stocktwits, retail sentiment around UBER fell from ‘extremely bullish’ to ‘bullish’ territory over the past 24 hours, while message volume rose from ‘high’ to ‘extremely high’ levels.<figure class="image"><img style="aspect-ratio:576/62;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_18_at_10_08_01_AM_png_8398df886d.webp" alt="UBER's Sentiment Meter and Message Volume as of 10:08 a.m. ET on Sept. 18, 2025 | Source: Stocktwits" width="576" height="62"><figcaption>UBER's Sentiment Meter and Message Volume as of 10:08 a.m. ET on Sept. 18, 2025 | Source: Stocktwits</figcaption></figure>A Stocktwits user expressed optimism on the stock, saying it’s “going higher for longer.”<stembedurl>https://stocktwits.com/trading__analysis/message/629113251</stembedurl>Another user believes the partnership is a “great move.”<stembedurl>https://stocktwits.com/RunGal/message/629113752</stembedurl>Uber noted on Thursday that Flytrex is one of only four drone delivery providers authorized by the Federal Aviation Administration (FAA) for beyond visual line of sight operations. The firm highlighted that it is making its first investment in drone technology with Flytrex to accelerate the development and deployment of drone delivery technology.According to Uber, Flytrex has completed over 200,000 deliveries across the U.S. Flytrex currently operates in North Carolina, Texas, and other approved locations. The company typically serves customers within a two- to three-mile radius of its fulfillment centers, and its drones can reach speeds of up to 32 km/h.Uber stock is up 57% this year and approximately 29% over the past 12 months.Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/bollinger-innovations-announces-1-for-250-reverse-stock-split/chDcxioR3b7">Bollinger Innovations Announces 1-For-250 Reverse Stock Split</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

A Uber car is seen on the street in Krakow, Poland, on March 6, 2025. (Photo by Klaudia Radecka/NurPhoto via Getty Images)

Uber Inks Partnership With Flytrex For Drone Delivery In US: Retail Sees Stock ‘Going Higher For Longer’

The company stated that drone delivery services are expected to begin with Uber Eats pilot markets in the U.S. by the end of the year.

Shares of Roivant (ROIV) jumped 9% on Wednesday after the company, along with Priovant Therapeutics, announced positive results from a late-stage trial evaluating Brepocitinib in dermatomyositis.Dermatomyositis is a multi-organ idiopathic inflammatory condition that affects approximately 50,000 adults in the U.S. and is characterized by debilitating muscle weakness and skin lesions. No targeted therapies are approved for the condition, and a majority of patients are treated with high-dose oral steroids.Once-daily oral Brepocitinib 30 mg demonstrated clinically meaningful and statistically significant improvement compared to placebo on the primary endpoint and all key secondary endpoints in the study, including measurements of skin disease, muscle disease, steroid-sparing effect, and rapidity of onset, the company said.On Stocktwits, retail sentiment around ROIV stock stayed within the ‘bullish’ territory over the past 24 hours, while message volume stayed at ‘high’ levels.<figure class="image"><img style="aspect-ratio:619/61;" src="https://news.stocktwits-cdn.com/Screenshot_2025_09_17_at_2_05_09_PM_png_94ffd6f84d.webp" alt="ROIV's Sentiment Meter and Message Volume as of 2:05 p.m. ET on Sept. 17, 2025 | Source: Stocktwits" width="619" height="61"><figcaption>ROIV's Sentiment Meter and Message Volume as of 2:05 p.m. ET on Sept. 17, 2025 | Source: Stocktwits</figcaption></figure>A Stocktwits user expressed optimism that the stock would rally further to $17.<stembedurl>https://stocktwits.com/StockBraker/message/628947861</stembedurl>Another user also cheered the stock’s rally over the past few weeks.<stembedurl>https://stocktwits.com/bbbloo/message/628950392</stembedurl>The company stated that 30mg of Brepocitinib achieved a week 52 mean Total Improvement Score (TIS) of 46.5 compared to 31.2 for placebo. It added that more than two-thirds of patients receiving the Brepocitinib 30 mg dose experienced at least a moderate response, with a TIS equal to or greater than 40, and nearly half experienced a major response, with a TIS equal to or exceeding 60.Furthermore, 42% of Brepocitinib 30 mg patients were able to discontinue steroids altogether, compared to 23% for the placebo, while 62% achieved a steroid dose of 2.5 mg or less per day. The safety profile observed in the study was consistent with that of previous trials, the company stated.The company plans to file for approval of the drug with the U.S. Food and Drug Administration for the treatment of dermatomyositis in the first half of 2026.ROIV stock is up 31% this year and approximately 28% over the past 12 months.&nbsp;Read also:&nbsp;<a href="https://stocktwits.com/news-articles/markets/equity/gm-in-talks-to-renew-jv-with-chinas-saic-report/chDGDTkRd6t">GM In Talks To Renew JV With China’s SAIC: Report</a>For updates and corrections, email newsroom[at]stocktwits[dot]com.

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

Roivant Stock Rises After Drug Achieves Goals In Late-Stage Study: Retail Sees Further Rally To $17

Once-daily oral Brepocitinib 30 mg demonstrated clinically meaningful and statistically significant improvement compared to placebo on the primary endpoint and all key secondary endpoints in the study, the company said. 

Duolingo (DUOL) shares were down nearly 4% in early trading on Wednesday, becoming the top trending ticker on Stocktwits after Citigroup lowered its price target on the stock to $375 from $400.Citigroup maintained a ‘Buy’ rating after attending the company’s annual global event Duocon 2025, according to TheFly. The firm believes that Duolingo's product announcements this year had a lower profile compared to past years.On Tuesday, Duolingo announced two major product updates at Duocon, primarily related to an integration that brings the Duolingo Score to LinkedIn Profiles, and the expansion of its Duolingo Chess course with an Android launch and a new player-versus-player mode on iOS.Retail sentiment on <a href="https://stocktwits.com/symbol/DUOL">Duolingo</a> improved to ‘bullish’ from ‘neutral’ territory a day ago, with message volumes at ‘high’ levels, according to data from Stocktwits.<figure class="image"><img style="aspect-ratio:797/102;" src="https://news.stocktwits-cdn.com/DUOL_sentiment_png_d242d7e2c6.webp" alt="DUOL sentiment.png" width="797" height="102"><figcaption>DUOL sentiment and message volume September 17, 2025, as of 10:15 am ET | Source: Stocktwits</figcaption></figure>A user on Stocktwits noted that they were considering accumulating Duolingo stock.<stembedurl>https://stocktwits.com/ChrisChristopherson/message/628956384</stembedurl>Citigroup stated that the company continues to enhance its platform, which should help drive engagement; however, the firm has reduced its Duolingo user forecasts to reflect trends in third-party apps.In August, Duolingo beat its second-quarter results and raised its annual forecasts, driven by an increase in daily active users on the app.Separately, media reports noted that Hungary’s competition authority was investigating Duolingo regarding misleading claims about the effectiveness of its platform.Another user on Stocktwits noted that the stock was in a “great spot to buy.”&nbsp;Shares of Duolingo have declined over 16% this year but have gained 8% in the last 12 months.For updates and corrections, email newsroom[at]stocktwits[dot]com.Also See: <a href="https://stocktwits.com/news-articles/markets/equity/amazon-rejigs-ai-assistant-for-online-sellers-report/chDGpY8Rd6L">Amazon Rejigs AI Assistant For Online Sellers: Report</a>

A laptop keyboard and Duolingo on App Store displayed on a phone screen are seen in this illustration photo. (Photo by Jakub Porzycki/NurPhoto via Getty Images)

Duolingo Stock Dips After Citigroup Lowers Price Target – Here’s What The Analyst Said About Duocon Event

Citigroup maintained a ‘Buy’ rating and noted that Duolingo's product announcements this year had a lower profile relative to the past.

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