Regeneron Pharmaceuticals
Private Company
Total funding raised: $40M
Overview
Regeneron is a premier biotechnology company with a mission to translate groundbreaking science into life-changing medicines for patients. Its achievements are anchored by its proprietary VelociSuite® technology platforms, which have enabled the development of a robust commercial portfolio and one of the industry's deepest pipelines. The company's strategy combines sustained internal R&D investment with selective, high-value collaborations, all supported by a fully integrated model from discovery to global commercialization.
Technology Platform
Proprietary VelociSuite® platform, including VelocImmune® (humanized mouse for fully human antibodies), VelociGene®, VelociMouse®, and Veloci-Bi® for bispecifics, integrated with the large-scale human genetics research of the Regeneron Genetics Center®.
Pipeline
200| Drug | Indication | Stage | Watch |
|---|---|---|---|
| REGN5713 + REGN5714 + REGN5715 + Placebo | Allergic Rhinitis | Phase 3 | |
| Mibavademab | Monogenic Obesity | Phase 3 | |
| REGN10933 + REGN10987 + Placebo | Healthy Participants | Phase 3 | |
| garetosmab | Fibrodyplasia Ossificans Progressiva (FOP) | Phase 3 | |
| rilonacept 160 mg + Placebo + rilonacept 160 mg | Familial Cold Autoinflammatory Syndrome (FCAS) | Phase 3 |
Funding History
1FDA Approved Drugs
9Opportunities
Risk Factors
Competitive Landscape
Regeneron competes with large pharma and biotech peers across its core areas: vs. Roche/Genentech in ophthalmology, vs. Merck/BMS in oncology, and vs. Amgen/AstraZeneca in immunology. Its integrated platform and genetics capability provide key differentiators.
Company Timeline
Founded in Tarrytown, United States
IPO — $40.0M
FDA Approval: EYLEA HD
FDA Approval: VEOPOZ
FDA Approval: LYNOZYFIC