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Sanofi

Sanofi logo
🇫🇷France
Ownership
Public
Employees
87.9K
Market Cap
$141.3B
Website
http://www.sanofi.com
Introduction

Sanofi engages in the research, production, and distribution of pharmaceutical products. It operates through the following business segments: Pharmaceuticals, Consumer Healthcare, and Vaccines. The Pharmaceuticals segment comprises the commercial operations of the following global franchises: specialty care, diabetes and cardiovascular, established prescription products and generics, and research, development, and production activities. The Consumer Healthcare segment includes the commercial operations for its Consumer Healthcare products. The Vaccines segment consists commercial operations of Sanofi Pasteur. The company was founded in 1973 and is headquartered in Paris, France.

Clinical Trials

1.5k

Active:82
Completed:1158

Trial Phases

5 Phases

Phase 1:265
Phase 2:307
Phase 3:537
+2 more phases

Drug Approvals

70

EMC:70

Drug Approvals

Epilim 100mg Crushable Tablets

Approval Date
Jul 7, 2025
EMC

Sabril 500 mg granules for oral solution

Approval Date
Jul 7, 2025
EMC

Renvela 2.4 g powder for oral suspension

Approval Date
Jul 7, 2025
EMC

Renagel 800 mg film-coated tablets

Approval Date
Jul 7, 2025
EMC

Sabril 500 mg film-coated tablets

Approval Date
Jul 7, 2025
EMC

Tritace 5mg Tablets

Approval Date
Jul 7, 2025
EMC

MenQuadfi solution for injection

Approval Date
Jul 7, 2025
EMC

Renvela 0.8 g powder for oral suspension

Approval Date
Jul 7, 2025
EMC
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Clinical Trials

Distribution across different clinical trial phases (1415 trials with phase data)• Click on a phase to view related trials

Phase 3
537 (38.0%)
Phase 2
307 (21.7%)
Phase 4
276 (19.5%)
Phase 1
265 (18.7%)
Not Applicable
30 (2.1%)

Rilzabrutinib for the Adult Participants With Chronic ITP Who Have Completed Phase 3 Study in Japan

Not Applicable
Not yet recruiting
Conditions
Immune Thrombocytopenia
Interventions
First Posted Date
2025-10-14
Last Posted Date
2025-10-14
Lead Sponsor
Sanofi
Target Recruit Count
4
Registration Number
NCT07216079

A Safety and Efficacy Study of a One-time Intravitreal Injection of SAR446597 in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration

Not Applicable
Recruiting
Conditions
Geographic Atrophy
Interventions
Drug: SAR446597
Drug: Sham Comparator
First Posted Date
2025-10-10
Last Posted Date
2025-10-20
Lead Sponsor
Sanofi
Target Recruit Count
104
Registration Number
NCT07215234
Locations
🇺🇸

Associated Retina Consultants - Peoria - DocTrials - PPDS- Site Number : 8400011, Peoria, Arizona, United States

🇺🇸

Vitreo Retinal Associates, P.A.- Site Number : 8400004, Gainesville, Florida, United States

A Post-marketing Surveillance Study of Beyfortus (Nirsevimab) in Republic of Korea

Not yet recruiting
Conditions
Respiratory Syncytial Virus
Interventions
First Posted Date
2025-10-01
Last Posted Date
2025-10-01
Lead Sponsor
Sanofi
Target Recruit Count
3000
Registration Number
NCT07200206

Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic Phenotype

Not Applicable
Recruiting
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Placebo
First Posted Date
2025-09-24
Last Posted Date
2025-10-14
Lead Sponsor
Sanofi
Target Recruit Count
942
Registration Number
NCT07190209
Locations
🇺🇸

Newport Native MD- Site Number : 8400003, Newport Beach, California, United States

🇺🇸

Helix Biomedics, LLC- Site Number : 8400065, Boynton Beach, Florida, United States

🇺🇸

MCR Research- Site Number : 8400004, Miami, Florida, United States

and more 8 locations

Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD), Characterized by an Eosinophilic Phenotype

Not Applicable
Recruiting
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Placebo
First Posted Date
2025-09-24
Last Posted Date
2025-10-14
Lead Sponsor
Sanofi
Target Recruit Count
942
Registration Number
NCT07190222
Locations
🇺🇸

Tucson Clinical Research Institute- Site Number : 8400006, Tucson, Arizona, United States

🇺🇸

Critical Care, Pulmonary and Sleep Associates- Site Number : 8400081, Lakewood, Colorado, United States

🇺🇸

Finlay Medical Research- Site Number : 8400107, Greenacres City, Florida, United States

and more 10 locations
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News

Electra Therapeutics' ELA026 Receives FDA Breakthrough Therapy and EMA Priority Designations for Rare Inflammatory Disease

Electra Therapeutics' ELA026 becomes the first investigational therapy to receive both FDA Breakthrough Therapy designation and EMA Priority Medicines designation for secondary hemophagocytic lymphohistiocytosis (sHLH).

Sanofi's Efdoralprin Alfa Achieves Primary Endpoints in Phase 2 Alpha-1 Antitrypsin Deficiency Study

Sanofi's efdoralprin alfa demonstrated statistically significant superiority over standard plasma-derived therapy in the ElevAATe phase 2 study, meeting all primary and key secondary endpoints for alpha-1 antitrypsin deficiency emphysema treatment.

Merck KGaA's Precem-TcT ADC Shows 31% Response Rate in Colorectal Cancer, Advances to Phase III

Merck KGaA's antibody-drug conjugate precemtabart tocentecan (Precem-TcT) demonstrated a 31% objective response rate in heavily pre-treated colorectal cancer patients at 2.8mg/kg dose during Phase I trials.

California Launches First State-Branded Insulin Program, Offering $55 Five-Pack to Combat High Drug Costs

California becomes the first state to sell its own brand of generic insulin through the CalRx program, with five-pack insulin pens available for $55 starting January 1, 2025.

CD40-Targeted Therapies Advance Toward First Approval by 2027 with Over 35 Candidates in Clinical Development

Over 35 CD40-targeted therapies are currently in clinical trials, with the first approval expected by 2027 according to new market research.

Cincinnati Children's Develops Human Liver Organoid Platform to Predict Immune-Mediated Drug Toxicity

Researchers at Cincinnati Children's Hospital Medical Center, in collaboration with Roche, have developed a next-generation human liver organoid microarray platform that integrates patient-specific genetics and immune responses to predict idiosyncratic drug-induced liver injury.

Dupilumab Reduces Severe COPD Exacerbations Regardless of Cardiovascular and Metabolic Comorbidities

Post hoc analysis of pooled BOREAS and NOTUS phase 3 trials demonstrates dupilumab's consistent efficacy in reducing COPD exacerbations by 31-33% regardless of cardiovascular or metabolic disease history.

Activist Investor Shah Capital Calls for Novavax Sale Amid COVID Vaccine Market Share Struggles

Shah Capital, Novavax's second-largest shareholder with a 7.2% stake, has urged the company's board to pursue a sale, citing three consecutive years of poor COVID-19 vaccine performance.

Ona Therapeutics Appoints ADC Development Veteran Dr. Antoine Yver as Board Chair to Advance Breast Cancer Pipeline

Ona Therapeutics has appointed Dr. Antoine Yver, a veteran with over 35 years of oncology drug development experience, as Chair of its Board of Directors to guide the company's transition to clinical-stage operations.

Innate Pharma Advances Lacutamab Toward Accelerated Approval for Rare T-Cell Lymphomas

Innate Pharma will host an investor event on October 28, 2025, to discuss lacutamab's path to potential accelerated approval in Sézary syndrome based on Phase 2 TELLOMAK trial data.

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