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Forecast
The analysts' average price target is €764.61 (-8.05%). The median is €763.01 (-8.24%).
| Buy |
35 |
| Hold |
14 |
| Sell |
0 |
News Go to news feed
Regeneron exceeds Q3 expectations significantly and hits 52-week high
Regeneron reports Q3 revenue up 36% to $5.1 billion and adjusted earnings per share of $20.07 versus $16.24 expected. Collaboration revenue with Sanofi, mainly from Dupixent, rose 68% to $2.72 billion. Strong contributions also came from Libtayo and the higher-dose Eylea, which boosted revenues by $550 million and $699 million respectively; the stock rises about 8% in premarket trading. » More on deraktionaer.de
Regeneron highlights EYLEA HD momentum, Dupixent growth and upcoming pipeline catalysts
Regeneron reported double-digit revenue and earnings growth with EYLEA HD comprising ~60% of EYLEA franchise sales and expected low- to mid-teens sequential demand growth in Q3 and Q4 despite biosimilar pressure. Dupixent is annualizing at about $24 billion and Libtayo grew over 30% year-over-year, strengthening position in U.S. lung cancer. Management flagged near-term catalysts including an FDA decision for cemdisiran in generalized myasthenia gravis in November, PNH data in Q4, Phase III and Phase II readouts in Factor XI and MASH programs, and melanoma data later this year. The company repurchased roughly $2 billion of stock in H1 and continues to prioritize pipeline funding, business development, dividends and buybacks. » More on finance.yahoo.com
Regeneron continues to rely on Dupixent for growth and advances pipeline and production expansion
Regeneron sees Dupixent as its main growth driver and expects about USD 22 billion for its US business in 2026, assuming a market penetration of roughly 15–20% in atopic dermatitis. EYLEA HD is gaining market share in the anti‑VEGF segment, while biosimilars are likely to intensify competition in 2026/2027. Key pipeline milestones include cemdisiran with an FDA decision for generalized myasthenia gravis in November 2026 and PNH and GA data at the end of 2026; several DUPIXENT follow‑on programs are planned. Regeneron is expanding production capacity in northern New York and is prioritizing capital allocation for internal research, selective acquisitions and share buybacks. » More on de.investing.com
Historical dividends Dividends
All dividend metrics All metricsFinancials
| (EUR) | June 2026 | YoY |
|---|---|---|
| Revenue | 3.76B | 20.56% |
| Gross profit | 3.25B | 21.95% |
| Net profit | 1.14B | 3.75% |
| EBITDA | 1.46B | 3.59% |
Fundamentals
| Metric | Value |
|---|---|
Market capitalization | €74.82B |
Number of shares | 102.95M |
52-week high/low | €766.88 - €527.87 |
Dividend yield | 0.38% |
Dividends TTM | €3.18 |
Beta | 0.24 |
P/E ratio | 19.44 |
PEG ratio | 62.44 |
P/B ratio | 2.66 |
P/S ratio | 5.40 |
Company profile
Regeneron Pharmaceuticals, Inc. discovers, invents, develops, manufactures, and commercializes medicines for treating various diseases worldwide. The company's products include EYLEA injection to treat wet age-related macular degeneration and diabetic macular edema; myopic choroidal neovascularization; and diabetic retinopathy, as well as macular edema following retinal vein occlusion, including macular edema following central retinal vein occlusion and macular edema following branch retinal vein occlusion. It also provides Dupixent injection to treat atopic dermatitis and asthma in adults and pediatrics; Libtayo injection to treat metastatic or locally advanced cutaneous squamous cell carcinoma;Praluent injection for heterozygous familial hypercholesterolemia or clinical atherosclerotic cardiovascular disease in adults; REGEN-COV for covid-19; and Kevzara solution for treating rheumatoid arthritis in adults. In addition, the company offers Inmazeb injection for infection caused by Zaire ebolavirus; ARCALYST injection for cryopyrin-associated periodic syndromes, including familial cold auto-inflammatory syndrome and muckle-wells syndrome; and ZALTRAP injection for intravenous infusion to treat metastatic colorectal cancer; and develops product candidates for treating patients with eye, allergic and inflammatory, cardiovascular and metabolic, infectious, and rare diseases; and cancer, pain, and hematologic conditions. It has collaboration and license agreements with Sanofi; Bayer; Teva Pharmaceutical Industries Ltd.; Mitsubishi Tanabe Pharma Corporation; Alnylam Pharmaceuticals, Inc.; Roche Pharmaceuticals; and Kiniksa Pharmaceuticals, Ltd., as well as has an agreement with the U.S. Department of Health and Human Services, as well as with Zai Lab Limited; Intellia Therapeutics, Inc.; Biomedical Advanced Research Development Authority; and AstraZeneca PLC. The company was incorporated in 1988 and is headquartered in Tarrytown, New York.
| Name | Regeneron Pharmaceuticals |
| CEO | Leonard S. Schleifer |
| Headquarters | Tarrytown,
ny USA |
| Website | |
| Sector | Health Care |
| Industry | Biotechnology |
| IPO | 09/12/2017 |
| Employees | 15,410 |
Ticker symbols
| Exchange | Symbol |
|---|---|
NASDAQ | REGN |
London Stock Exchange | 0R2M.L |
Frankfurt | RGO.F |
Düsseldorf | RGO.DU |
Hamburg | RGO.HM |
Milan | 1REGN.MI |
London | 0R2M.L |
SIX | RGO.SW |
München | RGO.MU |
Wien | REGN.VI |
XETRA | RGO.DE |
