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Sanofi-Aventis U.S. Llc

Sanofi-Aventis U.S. Llc logo
🇺🇸United States
Ownership
Subsidiary
Established
2004-08-01
Employees
10K
Market Cap
-
Website
http://www.sanofi-aventis.us

Clinical Trials

6

Active:4
Completed:1

Trial Phases

1 Phases

Phase 3:4

Drug Approvals

36

FDA:33
NMPA:3

Drug Approvals

Teriflunomide Tablets

Product Name
奥巴捷
Approval Number
国药准字HJ20180038
Approval Date
Jun 7, 2023
NMPA

Teriflunomide Tablets

Product Name
奥巴捷
Approval Number
国药准字HJ20180039
Approval Date
Jun 7, 2023
NMPA

Dronedarone Hydrochloride Tablets

Product Name
盐酸决奈达隆片
Approval Number
国药准字HJ20210084
Approval Date
Dec 20, 2021
NMPA

Clinical Trials

Distribution across different clinical trial phases (4 trials with phase data)• Click on a phase to view related trials

Phase 3
4 (100.0%)
No trials found

News

Q32 Bio Names Adrien Sipos as Interim CMO to Lead Alopecia Areata Drug Development

Q32 Bio appointed Adrien Sipos, M.D., Ph.D., as Interim Chief Medical Officer to oversee the ongoing SIGNAL-AA Phase 2a clinical trial of bempikibart for alopecia areata treatment.

Major Insulin Manufacturers Agree to $35 Monthly Price Caps in State Settlements

Sanofi and Novo Nordisk have reached settlements with Maine and Minnesota attorneys general to cap insulin prices at $35 per month through 2029.

Propionic Acid Supplementation Shows Promise in Multiple Sclerosis Treatment

Propionic acid, a short-chain fatty acid produced by gut bacteria, may play a beneficial role in multiple sclerosis (MS) pathology by influencing immune and nervous systems.

Advancements in Clinical Trials for Fabry Disease, C. difficile Infections, and Mydriasis

• Clinical trials are actively progressing for Fabry Disease, with companies like Idorsia and Sanofi Genzyme developing novel therapies. • Emerging treatments like Venglustat and Pegunigalsidase alfa are expected to significantly impact the Fabry Disease market in the coming years. • Research and development efforts are also focused on Clostridium Difficile Infections, with Vedanta Biosciences leading Phase 3 trials for VE303. • Mydriasis treatments are advancing, with companies like Eyenovia exploring solutions like MYDCOMBI for pupil dilation.

EU Approves Sanofi's Cablivi as First Targeted Therapy for Rare Blood Clotting Disorder aTTP

The European Commission has authorized Cablivi (caplacizumab) as the first specific treatment for acquired thrombotic thrombocytopenic purpura (aTTP), a rare and life-threatening blood clotting disorder.

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