Financial Performance
5Y price score: 22
The price score is a basic measure of the stock's performance against the S&P 500 Index over a five-year period.
A score of 100 indicates that the stock did as well as the S&P 500 Index.
A score below 100 means the stock underperformed the index, while a score above 100 means it outperformed the S&P 500.
10Y return: 82%
US$ Per
Share
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541.0
52-week range
821.1
Your model inputs
Your fair value & Margin of safety
To calculate fair value based on cost of capital and terminal growth assumptions above, please select free cash flow forecast.
Forecast:
Valuation
Free Cash Flow Yield
5.7 %
Dividend Yield TTM
0.5 %
Market cap $
$ 69,714
Price / Earnings TTM
16.5
Price / Book TTM
2.2
PEG TTM
2
Earnings growth and return
LTM
5YR
10YR
Total return (price & dividends)
23.7 %
16.6 %
82 %
Free cash flow per share growth
18 %
115.9 %
563.2 %
Earnings per share growth
8.2 %
35.9 %
651.4 %
Founded: 1,988
Employees: 15,158
Business Summary:
Latest Earnings Call Takeaways
2026 Q1 (Apr 29, 2026)
1) Financial Performance Highlights
- Regeneron reported a 19% increase in total revenues year-over-year, reaching $3.6 billion in Q1 2026.
- Non-GAAP earnings per share rose 15% to $9.47, with net income of $1 billion.
- Global net sales of DUPIXENT surged 31% to $4.9 billion, driven by strong demand across various indications.
- EYLEA HD U.S. net sales increased 52% to $468 million, while Libtayo sales grew 54% to $438 million.
2) Strategic Developments and Pipeline Progress
- Regeneron announced a $3 billion share repurchase program, reflecting confidence in its financial position.
- The company received FDA approval for Otarmeni, a gene therapy for genetic hearing loss, and committed to providing it for free.
- Positive Phase III data for cemdisiran in generalized myasthenia gravis was presented, with an FDA decision expected in Q4 2026.
- The FDA accepted the biologics license application for garetosmab for fibrodysplasia ossificans progressiva, with a decision anticipated in August 2026.
3) Challenges and Regulatory Updates
- The FDA did not act by the April 2026 PDUFA date for the EYLEA HD prefilled syringe application, which remains pending.
- A temporary interruption in manufacturing at the Limerick, Ireland site impacted GAAP gross margin, which was 76% for Q1.
- EYLEA's U.S. net sales declined 36% year-over-year, attributed to competitive pressures and patient affordability issues.
4) Market Position and Competitive Landscape
- DUPIXENT is positioned as the #1 biologic prescribed across multiple specialties, with annualized global net sales nearing $20 billion.
- EYLEA HD is noted for its broad label and dosing flexibility, contributing significantly to the retina franchise.
- Libtayo continues to gain traction in advanced non-small cell lung cancer and adjuvant CSCC, with strong physician adoption.
- Regeneron is exploring next-generation therapies, including long-acting antibodies and bispecifics targeting IL-4 and IL-13.
5) Guidance and Outlook
- Regeneron expects continued growth in DUPIXENT and EYLEA HD, with anticipated regulatory decisions on multiple pipeline candidates.
- The company remains committed to balancing investments in R&D with shareholder returns through share repurchases and dividends.
- Further details on specific pipeline candidates and their potential impact on future revenue were not fully disclosed during the call.
Bottom line: Regeneron's strong Q1 performance, driven by robust sales of DUPIXENT and EYLEA HD, alongside strategic investments and regulatory advancements, positions the company well for sustained growth and innovation in the biopharmaceutical space, making it an attractive prospect for shareholders.
Annual Reports, Presentations And IR Contacts
Go to the websiteRegeneron Pharmaceuticals — Financial Overview, Stock Price, Market Cap
Regeneron Pharmaceuticals is a company. Founded in 1988. As of July 20, 2026, the company's market capitalization is $69713957180 with a current stock price of $676.69.