Focus: Regeneron is a large-cap publicly traded biotechnology company with $13.1B in FY2025 revenue, headquartered in Tarrytown, NY, specializing in small molecules and biologics across ophthalmology, oncology, immunology, dermatology, and rare diseases.
Profile data last refreshed 22h ago · AI intelligence enriched 1w ago
Hot — 376 jobs added in 30d
Net +28 (376 new, 348 removed). Aggressive expansion phase.
Regeneron offers financial stability and research depth in a proven franchise, but career longevity depends on successful EYLEA HD transition and Phase 3 pipeline conversion amid high single-product revenue risk.
Flagship revenue engine representing 85% of company revenue; dominates wet AMD market but faces biosimilar and competitive pressure.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Generated by Claude from Regeneron's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
Specialized rare disease biologic with modest current uptake; represents portfolio diversification beyond ophthalmology.
Early immuno-oncology asset in skin cancer; limited scale but establishes oncology footprint.
Higher-concentration EYLEA formulation that outpaced legacy EYLEA in Q2 2026; critical indicator of franchise renewal and durability.
Recently approved complement therapy in rare hematologic disease; early-stage growth asset with orphan market protection.
Established cardiovascular agent with Phase 3 expansion into Type 2 Diabetes and coronary vessel disease.
Blockbuster immunology platform with Phase 3 trials ongoing in asthma and Phase 2/3 in bullous pemphigoid; most versatile asset in portfolio.
Rare public health asset approved for EVD; limited commercial scale but strong ESG and government contracting value.
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Source: USCIS H-1B Employer Data Hub
Recent peer-reviewed publications with author affiliations at this company
Dupilumab subgroup responder analysis: a post hoc analysis from LIBERTY PRIME and PRIME2 in prurigo nodularis.
Dupilumab treatment improves signs, symptoms, and quality of life in children aged 6 months to 11 years with moderate-to-severe atopic dermatitis: a plain language summary.
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Showing 5 of 10 publications
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