Paris, France · Est. 2004 · 91,000 employees
Global healthcare company focused on therapeutic solutions.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 4 drugs with upcoming expirations
Pipeline
By Phase
65 drugs in development
By Therapeutic Area
top 6
R&D Momentum
94/100
Pipeline Velocity
72/100
Trial Completion Rate
87/100
Pipeline Concentration
14/100
Pipeline Freshness
70/100
Strategic Signals
Activity
Last 14 days
A Multinational, Multicenter, Double-blind, Placebo-controlled Phase 2 Study to Evaluate Efficacy and Safety of SAR444656 in Adult Participants With Moderate to Severe Atopic Dermatitis
Atopic Dermatitis Disease Registry of Adult and Adolescent Patients Initiating or Switching Systemic Treatments
A Phase 2b, Multi-national, Multi-center, Randomized, Double-blind, Placebo-controlled, Dose-ranging Study Followed by a Long-term Extension to Evaluate the Efficacy and Safety of Brivekimig in Adult Participants With Moderate to Severe Ulcerative Colitis
A Randomized, Double-blind, Placebo-controlled, Multi-center Phase 2b Study With a Blinded Extension and an Optional Open-label Extension-Assessing the Safety and Efficacy of Frexalimab, a CD40L-antagonist Monoclonal Antibody, for the Preservation of Pancreatic β-cell Function in Adults and Adolescents With Newly Diagnosed Type 1 Diabetes on Insulin Therapy
A Phase 1, Randomized, Placebo-controlled, Multi-arm, Study to Evaluate the Safety of a Chlamydia Trachomatis mRNA Vaccine Candidate in Adults
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-ranging Study to Evaluate the Efficacy and Safety of Brivekimig in Adults With Moderate to Severe Crohn's Disease
Major Adverse Cardiovascular Events in Patients With Atherosclerotic Cardiovascular Disease Without Prior Ischemic Events: Rates, Risk Factors, and Patient Characteristics From Routine Clinical Practice Data Sources
Major Adverse Cardiovascular Events in Patients With Atherosclerotic Cardiovascular Disease Without Prior Ischemic Events: Rates, Risk Factors, and Patient Characteristics From Routine Clinical Practice Data Sources
Major Adverse Cardiovascular Events in Patients With Atherosclerotic Cardiovascular Disease Without Prior Ischemic Events: Rates, Risk Factors, and Patient Characteristics From Routine Clinical Practice Data Sources
Phase 1, Single Center, Open-label, Randomized, Parallel-group Study to Evaluate Pharmacokinetics and Tolerability of a Single Subcutaneous Dose of Dupilumab Coformulated With Berahyaluronidase Alfa and Dupilumab Without Berahyaluronidase Alfa in Healthy Participants
A Single-arm Extension Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Lunsekimig in Adult Participants With Inadequately Controlled Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) Who Completed a Previous Lunsekimig CRSwNP Clinical Study
Details
Company Overview
$140.0B
Mkt Cap
$43.1B
Revenue
$11.2B
Cash
Therapeutic Focus
Pipeline
Regulatory
Rifadin — RIFADIN
Application NDA050627
Avalglucosidase alfa — NEXVIAZYME
Application BLA761194
Plavix — PLAVIX
Application NDA020839
Isoproterenol Hydrochloride — ISOPROTERENOL HYDROCHLORIDE
Application ANDA210322
Rifadin — RIFADIN
Application NDA050627
Rifadin — RIFADIN
Application NDA050627
Isoproterenol Hydrochloride — ISOPROTERENOL HYDROCHLORIDE
Application ANDA217648
Isoproterenol Hydrochloride — ISOPROTERENOL HYDROCHLORIDE
Application ANDA210576
glutamine — L-GLUTAMINE
Application ANDA215647
Jevtana — CABAZITAXEL
Application NDA207970 (NDA)
Sutimlimab — ENJAYMO
Application BLA761164
Rifadin — RIFADIN
Application NDA050627
Rifadin — RIFADIN
Application NDA050627
Avapro — AVAPRO
Application NDA020757
glutamine — ENDARI
Application NDA208587
Isoproterenol Hydrochloride — ISOPROTERENOL HYDROCHLORIDE
Application ANDA211864
glutamine — L-GLUTAMINE
Application ANDA215647
Avapro — AVAPRO
Application NDA020757
glutamine — L-GLUTAMINE
Application ANDA219722
glutamine — L-GLUTAMINE
Application ANDA219750
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)