Tarrytown, New York, United States · Est. 1988 · 13,000 employees
Regeneron is a biotechnology company that discovers, develops, and commercializes medicines for serious medical conditions using proprietary technologies and platforms.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Pipeline
By Phase
40 drugs in development
By Therapeutic Area
top 6
R&D Momentum
89/100
Pipeline Velocity
69/100
Trial Completion Rate
78/100
Pipeline Concentration
15/100
Pipeline Freshness
75/100
Strategic Signals
Activity
Last 14 days
A Phase 3b Single-Arm Study of Aflibercept 8 mg in Participants With Neovascular Age-Related Macular Degeneration (nAMD) or Diabetic Macular Edema (DME)
A Multicenter, Randomized, Double-Masked, Placebo-Controlled Phase 3 Study of the Efficacy, Safety, and Tolerability of Subcutaneously Administered Pozelimab in Combination With Cemdisiran or Cemdisiran Alone in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration
An Open-Label Extension Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of Pozelimab and Cemdisiran Combination Therapy in Patients With Paroxysmal Nocturnal Hemoglobinuria
A Master Protocol for a Phase 3, Randomized, Multicenter, Double-blind Study to Assess Stroke and Systemic Embolism Prevention With REGN7508 and REGN9933, Monoclonal Antibodies Against Factor XI, Versus Placebo in Participants With Atrial Fibrillation for Whom Oral Anticoagulation is Unsuitable (ROXI-INCLINE)
A Phase 3 Randomized Study of Intralesional Cemiplimab Versus Primary Surgery in Participants With Early Stage Cutaneous Squamous Cell Carcinoma (CSCC)
A Phase 3, Randomized, Multicenter, Double-blind Study to Assess Stroke and Systemic Embolism Prevention With REGN7508, a Monoclonal Antibody Against Factor XI, Versus Apixaban in Participants With Atrial Fibrillation (ROXI-EVEREST)
A Phase 1/2 Study of REGN5093 in Patients With MET-Altered Advanced Non-Small Cell Lung Cancer
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess Efficacy and Safety of REGN7508, a Monoclonal Antibody Against FXI, for Primary Prophylaxis of Cancer-Associated Thrombosis for Participants With Solid Tumors Undergoing Cancer Treatment (ROXI-CAT-I)
A Phase 2, Randomized, Multicenter, Open-label, Blinded-endpoint Study to Evaluate the Safety of REGN7508 and REGN9933, Monoclonal Antibodies Against FXI, Versus Apixaban in Participants With Atrial Fibrillation (ROXI-ATLAS)
A Phase 3, Randomized, Open-Label Study of Linvoseltamab Versus Daratumumab in Participants With Smoldering Multiple Myeloma at High Risk of Developing Multiple Myeloma
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamic Effects of REGN13335, an Anti-PDGF-B Monoclonal Antibody, in Adults With Pulmonary Arterial Hypertension
A Phase 3, Multicenter, Randomized, Open-Label, Study to Evaluate REGN7508, A Factor XI Monoclonal Antibody, Versus Apixaban and Enoxaparin for Prophylaxis of Venous Thromboembolism After Elective Total Knee Arthroplasty (ROXI-APEX)
Details
Company Overview
$115.0B
Mkt Cap
$13.5B
Revenue
$6.8B
Cash
Therapeutic Focus
Pipeline
Regulatory
Praluent — PRALUENT
Application BLA125559
Praluent — PRALUENT
Application BLA125559
Libtayo — LIBTAYO
Application BLA761097
Libtayo — LIBTAYO
Application BLA761097
Fabhalta — FABHALTA
Application NDA218276
Eylea — EYLEA HD
Application BLA761355 (BLA)
VEOPOZ — VEOPOZ
Application BLA761339 (BLA)
Libtayo — LIBTAYO
Application BLA761097
Libtayo — LIBTAYO
Application BLA761097
Fabhalta — FABHALTA
Application NDA218276
Libtayo — LIBTAYO
Application BLA761097
Fabhalta — FABHALTA
Application NDA218276
Praluent — PRALUENT
Application BLA125559
Libtayo — LIBTAYO
Application BLA761097
Libtayo — LIBTAYO
Application BLA761097
Praluent — PRALUENT
Application BLA125559
Libtayo — LIBTAYO
Application BLA761097
Fabhalta — FABHALTA
Application NDA218276
Libtayo — LIBTAYO
Application BLA761097
Fabhalta — FABHALTA
Application NDA218276
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)