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Regeneron Pharmaceuticals

Regeneron Pharmaceuticals logo
🇺🇸United States
Ownership
Public
Established
1988-01-01
Employees
13.4K
Market Cap
$132.4B
Website
http://www.regeneron.com
Introduction

Regeneron Pharmaceuticals, Inc. is a biotechnology company, which engages in the discovery, invention, development, manufacture, and commercialization of medicines. Its product portfolio includes the following brands: Dupixent, Evkeeza, Eylea, Inmazeb, and Kevzara. The firm accelerates the traditional drug development process through its proprietary VelociSuite technologies such as VelocImmune, which uses unique genetically humanized mice to produce optimized fully human antibodies and bispecific antibodies. The company was founded by Alferd G. Gilman, Leonard S. Schleifer, George Damis Yancopoulos, and Eric M. Shooter on January 8, 1988, and is headquartered in Tarrytown, NY.

Clinical Trials

745

Active:363
Completed:218

Trial Phases

5 Phases

Phase 1:436
Phase 2:104
Phase 3:99
+2 more phases

Drug Approvals

5

FDA:5

Drug Approvals

Praluent

Approval Date
Mar 8, 2024
FDA

LIBTAYO

Approval Date
Mar 4, 2024
FDA

EYLEA

Approval Date
Dec 14, 2023
FDA

Evkeeza

Approval Date
Mar 30, 2023
FDA

Inmazeb

Approval Date
Dec 20, 2022
FDA

Clinical Trials

Distribution across different clinical trial phases (662 trials with phase data)• Click on a phase to view related trials

Phase 1
436 (65.9%)
Phase 2
104 (15.7%)
Phase 3
99 (15.0%)
Phase 4
10 (1.5%)
Not Applicable
7 (1.1%)
phase_1_2
4 (0.6%)
phase_2_3
2 (0.3%)

A Study to Evaluate How Pozelimab + Cemdisiran Combination Therapy Works in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Whose Current Treatment is Not Working Efficiently

Not Applicable
Not yet recruiting
Conditions
Paroxysmal Nocturnal Hemoglobinuria
Interventions
First Posted Date
2025-09-04
Last Posted Date
2025-09-04
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
35
Registration Number
NCT07154745

A Study to Investigate Ubamatamab With and Without REGN7075 in Adult Participants With Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)

Not Applicable
Not yet recruiting
Conditions
Advanced/Metastatic Non-Small Cell Lung Cancer
Interventions
First Posted Date
2025-09-04
Last Posted Date
2025-09-04
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
300
Registration Number
NCT07154290

A Study to Test the Safety of Pozelimab in Pediatric Participants 1 to 5 Years of Age With a Rare Disease Called CHAPLE (Complement Hyperactivation, Angiopathic Thrombosis, Protein-losing Enteropathy) Disease

Not Applicable
Not yet recruiting
Conditions
CHAPLE Disease
Interventions
First Posted Date
2025-08-26
Last Posted Date
2025-08-26
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
5
Registration Number
NCT07142343

A Study of Dupilumab in Small Children With an Allergic Condition of the Esophagus (Food Pipe): Eosinophilic Esophagitis

Not Applicable
Recruiting
Conditions
Eosinophilic Esophagitis (EoE)
Interventions
First Posted Date
2025-08-08
Last Posted Date
2025-09-04
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
20
Registration Number
NCT07112378
Locations
🇺🇸

GI Care for Kids LLC, Atlanta, Georgia, United States

Incidence of Retinal Vasculitis Among Patients Receiving Aflibercept: A US Real-World Evidence Study

Recruiting
Conditions
Retinal Vasculitis
Interventions
First Posted Date
2025-08-05
Last Posted Date
2025-08-05
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
290000
Registration Number
NCT07105228
Locations
🇺🇸

Regeneron Research Site, Tarrytown, New York, United States

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News

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Dualitas Therapeutics launched from stealth with $65 million Series A funding co-led by Versant Ventures and Qiming Venture Partners USA, with participation from Eli Lilly and Company and other strategic investors.

Regeneron's Libtayo Combination Therapy Demonstrates 19.4% Five-Year Survival Rate in Advanced Lung Cancer

Regeneron's Phase 3 EMPOWER-Lung 3 trial shows Libtayo plus chemotherapy achieved a 19.4% five-year survival rate compared to 8.8% with chemotherapy alone in advanced non-small cell lung cancer patients.

Sandoz Secures Patent Settlement with Regeneron, Clears Path for Aflibercept Biosimilar Launch by End of 2026

Sandoz reached a patent settlement agreement with Regeneron resolving all litigation related to its FDA-approved aflibercept biosimilar Enzeevu, clearing the path for US market entry by the fourth quarter of 2026.

Regeneron's First-in-Class Allergen-Blocking Antibodies Show 52% Reduction in Cat Allergy Symptoms in Phase 3 Trials

Regeneron's investigational allergen-blocking antibodies achieved significant symptom reduction in Phase 3 trials, with cat allergy treatments reducing ocular itch by 52% and birch allergy treatments reducing itch by 51% compared to placebo.

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The FDA issued a Form 483 to Novo Nordisk's Bloomington, Indiana manufacturing facility following an inspection that identified contamination issues including cat and human hair in vial stoppers and pest infestations in classified areas.

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Immuneering Corporation announced a clinical supply agreement with Eli Lilly to evaluate atebimetinib in combination with olomorasib in a planned Phase 2 trial for advanced KRAS G12C-mutant non-small cell lung cancer patients.

FDA Inspection Reveals Contamination Issues at Novo Nordisk's Indiana Manufacturing Plant

FDA inspection found cat hair, pests, bacteria, and equipment failures at a Novo Nordisk manufacturing plant in Bloomington, Indiana, that was acquired from Catalent last year.

Johnson & Johnson Commits $2 Billion to North Carolina Manufacturing Facility in Major US Investment Push

Johnson & Johnson will invest $2 billion over 10 years to build a 160,000+ square foot manufacturing facility at Fujifilm Biotechnologies' new Holly Springs, North Carolina site.

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