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- $81.4BMarket Cap
- 40.00%1-Year Change
- BiotechnologyIndustry
Regeneron Pharma (REGN)
Key Performance
More- Earnings Score: 52
- Momentum Score: 30
- True Yield: N/A
- Financial Health Score: 0
Latest Research & News
Regeneron Pharmaceuticals has extended its agreement with BARDA to supply additional doses of Inmazeb, its FDA-approved Ebola treatment, through 2031 for approximately $270 million. The company is also advancing maftivimab, a component of Inmazeb, as a potential monotherapy treatment for Bundibugyo virus disease in the current outbreak in the Democratic Republic of the Congo.
10/26/2026, 7:00 AM • GlobeNewswire
Regeneron announced longer-term data (44-month follow-up) from the Phase 3 C-POST trial showing Libtayo (cemiplimab) as adjuvant treatment for high-risk cutaneous squamous cell carcinoma demonstrated a 37% reduction in risk of death compared to placebo, with sustained disease-free survival benefits. The drug was approved by the FDA in October 2025 and European Commission in November 2025 as the first immunotherapy for this indication.
10/25/2026, 5:15 AM • GlobeNewswire
A Motley Fool podcast discusses how historical S-1 risk factors from Amazon, Alphabet, and Meta didn't materialize into existential threats, offering perspective on Anthropic's alarming AI risks. The hosts identify stocks hitting new lows amid market fear—including Brookfield Corporation, Shopify, and Realty Income—while explaining how rising bond yields create both challenges for growth stocks and opportunities for cash-rich businesses and financial institutions.
10/23/2026, 10:29 AM • The Motley Fool
Forget Eli Lilly and Novo: This Biotech Could Be a Surprising Winner in the Weight Loss Market
Regeneron Pharmaceuticals is emerging as a competitive player in the rapidly growing weight loss market with two differentiated candidates: olatorepatide, which shows better gastrointestinal tolerability than competitors with 19% mean weight loss, and trevogrumab, designed to preserve lean muscle mass alongside anti-obesity drugs. Beyond weight loss, Regeneron's strong pipeline including Dupixent and newer Eylea HD formulation positions it for medium-term growth.
10/19/2026, 10:24 AM • The Motley Fool
Forget Eylea: Regeneron's Real Value May Be Hiding in Its Dupixent Profit Share
Despite declining Eylea sales, Regeneron's strong performance is driven by Dupixent, a blockbuster drug developed with Sanofi that generated $6 billion in global sales with 38% year-over-year growth. The company's Q2 revenue grew 17% to $4.3 billion, with Dupixent collaboration revenue jumping 51%. While Dupixent faces biosimilar competition in the early 2030s, Regeneron plans to defend its market position through improved formulations, pipeline replacements, and promising candidates like olatorepatide in the weight-loss market.
10/17/2026, 3:24 PM • The Motley Fool
The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a positive opinion recommending approval of an alternative dosing schedule for Libtayo (cemiplimab) across all approved cancer indications. The new regimen allows for extended dosing of 700 mg every six weeks after an initial 12-week treatment with 350 mg every three weeks, and optional reduction of infusion time to 15-30 minutes. The European Commission is expected to make a final decision in the coming months.
10/16/2026, 7:00 AM • GlobeNewswire
Pomerantz LLP is investigating securities fraud claims against EyePoint, Inc. following the company's announcement that its Phase 3 clinical trial for DURAVYU failed to meet its primary endpoint against Regeneron's Eylea. The stock plummeted 66.98% to $4.87 per share on August 17, 2026.
10/06/2026, 5:36 PM • GlobeNewswire
Regeneron announced presentations of new clinical research at ESMO Congress 2026, highlighting late-breaking Phase 3 data for Libtayo (cemiplimab) in cutaneous squamous cell carcinoma, Phase 2 neoadjuvant treatment data, and new research on Factor XI antibodies for cancer-associated thrombosis. The company is presenting 10 abstracts covering trials in CSCC, NSCLC, ovarian cancer, melanoma, and cancer-associated thrombosis.
10/06/2026, 7:00 AM • GlobeNewswire
Communiqué de presse : Mise en ligne du document «Q3 2026 aide-mémoire »
Sanofi announced the publication of its Q3 2026 aide-mémoire on October 6, 2026, with full quarterly results to follow on October 30, 2026. The company also announced expansions of strategic alliances with Regeneron for next-generation immunology antibodies and with Cheplapharm for mature medicines partnerships.
10/06/2026, 1:30 AM • GlobeNewswire
Press Release : Availability of the aide-mémoire for Q3 2026 results
Sanofi announced the availability of its Q3 2026 results aide-mémoire on October 6, 2026, with full results to be published on October 30, 2026. The company also announced expansions of strategic partnerships with Regeneron for next-generation immunology antibodies and with Cheplapharm for mature medicines.
10/06/2026, 1:30 AM • GlobeNewswire
Royalty Pharma Owns a Piece of 16 Blockbuster Drugs -- Is the Stock a Buy?
Royalty Pharma (RPRX) offers investors diversified exposure to blockbuster drugs through a unique royalty-based investment model. With strong returns on invested capital (14.9% average ROIC), ownership in 16 blockbuster drugs, and analyst forecasts suggesting significant multiple expansion potential, the stock appears undervalued despite a 50% year-to-date surge. However, risks include share dilution and increasing competition in the pharma royalty space.
10/01/2026, 12:30 PM • The Motley Fool
The HoFH market is expected to expand through 2036, driven by improved genetic screening, earlier diagnosis, and adoption of targeted lipid-lowering therapies. With approximately 1,840 diagnosed prevalent cases in the 7MM in 2025, the market is shifting toward long-acting, receptor-independent therapies including RNA interference agents and ANGPTL3 inhibitors. Key unmet needs include limited treatment efficacy for patients with minimal LDL receptor function, delayed diagnosis, and high treatment burden.
09/30/2026, 4:59 AM • GlobeNewswire
Should You Buy Regeneron Pharmaceuticals Stock Before Oct. 30?
Regeneron Pharmaceuticals stock has underperformed this year, down around 1%, but the company demonstrated strong fundamentals in its last earnings report with 17% revenue growth and impressive drug sales. With a modest valuation (19x trailing earnings vs. S&P 500's 23x), a robust pipeline of 50 product candidates, and upcoming Q3 earnings on Oct. 30, analysts suggest the stock could be poised for a rally and represents a solid value buy for long-term investors.
09/28/2026, 1:05 PM • The Motley Fool
Is Regeneron Stock a Bargain Below $800?
Regeneron Pharmaceuticals' stock has declined from over $1,000 to below $800 over the past two years, primarily due to challenges with its Eylea product facing biosimilar competition. However, the company shows strong fundamentals with 17% revenue growth driven by Dupixent, successful mitigation of Eylea losses through its HD formulation, and promising pipeline candidates including the weight-loss drug olatorepatide. The analyst views the stock as attractive at current levels given its long-term growth prospects and shareholder return programs.
09/22/2026, 3:15 PM • The Motley Fool
A comprehensive market research report analyzing co-development deals in pharmaceuticals and biotechnology from 2016-2026 has been released. The report covers deal structures, financial terms, the top 25 most active dealmakers, and provides access to actual SEC-filed contract documents. Co-development partnerships are highlighted as a strategic approach for companies to share R&D costs, risks, and commercial opportunities while accelerating product development timelines.
09/22/2026, 10:59 AM • GlobeNewswire
Peers
Statistics
MoreInformation as of 10/23/2026
Company Profile
Regeneron Pharmaceuticals, Inc. discovers, invents, develops, manufactures, and commercializes medicines to treat various diseases worldwide. The company develops product candidates to treat eye, allergic and inflammatory, cardiovascular, metabolic, neurological, infectious, and rare diseases; and cancer, hematologic conditions. It also offers EYLEA injections for wet age-related macular degeneration and diabetic macular edema; myopic choroidal neovascularization; diabetic retinopathy; neovascular glaucoma; retinopathy of prematurity; Dupixent injection to treat atopic dermatitis and asthma; Libtayo injection for metastatic or locally advanced cutaneous squamous cell carcinoma; Praluent injection to treat heterozygous familial hypercholesterolemia (HoFH); and Kevzara solution for rheumatoid arthritis. It has license and collaboration agreement with Bayer for the development and commercialization of EYLEA 8 mg and EYLEA; Alnylam Pharmaceuticals, Inc. to discover, develop, and commercialize RNAi therapeutics for diseases by addressing therapeutic disease targets expressed in eye and central nervous system; Intellia Therapeutics, Inc. to advance CRISPR/Cas9 gene-editing technology for in vivo therapeutic development for therapies focused on neurological and muscular diseases; Hansoh Pharmaceuticals Group Company Limited to acquire development and commercial rights for HS-20094, a dual GLP-1/GIP receptor; and Tessera Therapeutics, Inc. develops and commercializes TSRA-196, an investigational gene editing therapy for Alpha-1 antitrypsin deficiency. The company has a strategic collaboration with Telix Pharmaceuticals Limited to develop and commercialize radiopharmaceutical therapies. It also has a strategic collaboration with CytomX Therapeutics, Inc. to create conditionally-activated bispecific cancer therapies. It has a strategic alliance with Sanofi to develop long-acting immunology antibodies. The company was incorporated in 1988 and is based in Tarrytown, New York.
Key Executives
- Leonard S. Schleifer
- George D. Yancopoulos
- Joseph J. LaRosa
- Daniel Van Plew
- Andrew J. Murphy
Current Ownership Distribution
- Mutual Funds2.4B (57.89%)
- Institutions1.7B (41.69%)
- Insiders17.7M (0.42%)
- Other0 (0.00%)