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Regeneron Pharmaceuticals, Inc.

REGN· NASDAQ
$759.24-0.44%
2026-08-03

Financials

Valuation Metrics

Regeneron Pharmaceuticals, Inc.'s Market Cap is $79.60B. At end of 2025 it was $79.33B. Ranked #217 of 3,112 in US market (top 7%), #67 of 1,445 on NASDAQ (top 5%), #15 of 269 in Pharmaceuticals, Biotechnology & Life Sciences (top 6%) by Market Cap.

Investment Metrics(as of 2026-08-03)

MetricValue
Size
Market Cap$79.60B
Revenue$15.53B
Net Income$4.33B
Total Assets$41730.60
Net Assets$31.26B
Employees15,410
Value
P/E18.39x
P/B2.55x
P/S5.12x
EV/EBITDA15.74x
FCF Yield4.42%
Profitability
ROE13.85%
Op. Margin24.74%
Revenue Growth16.73%
Earnings Growth-6.81%
Financial Health
Debt Ratio0.00%
Total Debt$1986.60
FCF$3.52B
Cash$2455.80
Current Ratio3.34x
Net Debt/EBITDA0.00x
Dividend
Div. Yield0.48%
Performance
1Y Return36.39%
1M Return16.04%
From 52W High-7.42%
1Y MDD-25.96%
Trading
Volume655,906 shares
Trading Value$500M
Per Share
EPS$43.78
BPS$303.76

Company Info

CEO Dr. Leonard S. Schleifer M.D., Ph.D.
Employees 15,410
HQ Tarrytown, United States

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 the 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 was incorporated in 1988 and is based in Tarrytown, New York.