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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:79
Completed:1151

Trial Phases

5 Phases

Phase 1:266
Phase 2:307
Phase 3:537
+2 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (1395 trials with phase data)• Click on a phase to view related trials

Phase 3
537 (38.5%)
Phase 2
307 (22.0%)
Phase 4
276 (19.8%)
Phase 1
266 (19.1%)
Not Applicable
9 (0.6%)

A Study to Investigate Airway Inflammation With Dupilumab Subcutaneously in Participants Aged ≥40 to ≤85 Years With Chronic Obstructive Pulmonary Disease.

Not Applicable
Not yet recruiting
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Placebo
First Posted Date
2025-07-08
Last Posted Date
2025-07-08
Lead Sponsor
Sanofi
Target Recruit Count
218
Registration Number
NCT07053423

Study to Evaluate Long-term Effectiveness and Safety, Patient Characteristics and Subjective Patient-reported Outcomes of Dupilumab in Patients With Chronic Obstructive Pulmonary Disease (COPD) Under Real-world Conditions

Not yet recruiting
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
First Posted Date
2025-07-04
Last Posted Date
2025-07-04
Lead Sponsor
Sanofi
Target Recruit Count
350
Registration Number
NCT07052396

Early Detection of Type 1 Diabetes in First Degree Relatives of Type 1 Diabetes Patients (DETECT T1D GULF)

Not Applicable
Not yet recruiting
Conditions
Type 1 Diabetes
First Posted Date
2025-06-26
Last Posted Date
2025-06-26
Lead Sponsor
Sanofi
Target Recruit Count
3500
Registration Number
NCT07038473

Study to Evaluate the Efficacy and Safety of Oral Rilzabrutinib in Adults With Immune Thrombocytopenia (ITP) Who Failed First-line Treatment

Phase 3
Not yet recruiting
Conditions
Immune Thrombocytopenia
Interventions
First Posted Date
2025-06-06
Last Posted Date
2025-06-06
Lead Sponsor
Sanofi
Target Recruit Count
60
Registration Number
NCT07007962

Phase 3 Randomized, Modified Double-blind, Active-controlled Safety Study on vYF in Adults

Phase 3
Recruiting
Conditions
Yellow Fever Immunization
Interventions
Biological: Yellow fever vaccine (live)
Biological: YF vaccine (live)
First Posted Date
2025-06-03
Last Posted Date
2025-06-19
Lead Sponsor
Sanofi
Target Recruit Count
640
Registration Number
NCT07002060
Locations
🇺🇸

Velocity Clinical Research-New Orleans- Site Number : 8400004, New Orleans, Louisiana, United States

🇺🇸

Rochester Clinical Research- Site Number : 8400005, Rochester, New York, United States

🇺🇸

Velocity Clinical Research - Providence- Site Number : 8400003, East Greenwich, Rhode Island, United States

and more 1 locations
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News

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Renasant Bio secured $54.5 million in seed funding from investors including 5AM Ventures, Atlas Venture, OrbiMed and Qiming Venture Partners USA to develop treatments for autosomal dominant polycystic kidney disease (ADPKD).

Sanofi Launches Long-term Safety Study for TZIELD in Stage 2 Type 1 Diabetes Patients

Sanofi has initiated an observational study to evaluate the long-term safety and efficacy of TZIELD (teplizumab-mzwv) in patients with Stage 2 Type 1 Diabetes.

EPO and UPC Reach Opposite Conclusions on Amgen's PCSK9 Antibody Patent Validity

The European Patent Office (EPO) Opposition Division upheld Amgen's PCSK9 antibody patent EP 3666797, finding it inventive, while the Unified Patent Court (UPC) Central Division revoked the same patent for lacking inventive step.

bluebird bio Strengthens Leadership Team with Three Key Executive Appointments

bluebird bio, a pioneer in gene therapies for severe genetic diseases, has appointed three new executives to strengthen its leadership team as the company focuses on commercial execution.

ESTEVE Acquires Caprelsa Rights from Sanofi to Expand Rare Cancer Treatment Portfolio

ESTEVE has entered into an agreement with Sanofi to acquire Caprelsa® (vandetanib) rights in more than 50 countries for treating aggressive and symptomatic medullary thyroid cancer in adults and children above 5 years of age.

Alzheimer's Drug Market Sees 780% Investment Surge Following Leqembi and Kisunla Approvals

Total M&A deal value in Alzheimer's disease jumped from $2 billion in 2022 to $18 billion in 2024, representing a 780% increase following the approval of disease-modifying treatments.

Vor Bio Secures Global Rights to Telitacicept in $4+ Billion Deal with RemeGen

Vor Bio acquired exclusive global rights (excluding Greater China) to develop and commercialize telitacicept, a dual-target fusion protein approved in China for multiple autoimmune diseases including generalized myasthenia gravis.

CDC's Reconstituted Vaccine Advisory Panel Votes to Eliminate Thimerosal from All Flu Vaccines

The newly appointed Advisory Committee on Immunization Practices (ACIP) voted 5-1 to recommend thimerosal-free influenza vaccines for all age groups, despite the preservative being present in only 6% of U.S. flu vaccines.

MIRA Pharmaceuticals Unveils Preclinical Data for SKNY-1, Targeting Obesity and Smoking Cessation Without CNS Side Effects

MIRA Pharmaceuticals announced new in vitro preclinical data from Eurofins demonstrating SKNY-1's potential as a first-in-class oral therapy for obesity and nicotine addiction without central nervous system side effects.

Sanofi Advances Kymera's Next-Generation IRAK4 Degrader KT-485 to Clinical Testing

Sanofi has selected Kymera's KT-485, a next-generation oral IRAK4 degrader, to advance into Phase 1 clinical testing next year for immuno-inflammatory diseases.

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