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  • sanofi

Tag: sanofi

You Searched For "sanofi"
USFDA grants priority review to Sanofi-Regeneron Dupixent for bullous pemphigoid

CDSCO Panel grants Sanofi's Protocol Amendment Proposal for Quadrivalent Meningococcal Conjugate Vaccine

Dr. Divya Colin19 March 2023 5:45 PM IST
New Delhi: The Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has approved Sanofi Healthcare's...
Itepekimab met primary endpoint in one of two COPD phase 3 studies: Sanofi, Regeneron

Sanofi cuts US list price of Lantus, its most-prescribed insulin by 78 percent

Ruchika Sharma17 March 2023 12:15 PM IST
Paris: Sanofi has announced that it will cut the list price of Lantus (insulin glargine injection) 100 Units/mL, its most widely prescribed insulin in...
Sanofi to acquire Provention Bio for USD 2.9 billion

Sanofi to acquire Provention Bio for USD 2.9 billion

Ruchika Sharma13 March 2023 3:30 PM IST
Paris: Sanofi and Provention Bio, Inc have entered into an agreement under which Sanofi has agreed to acquire Provention Bio, Inc., for $25.00 per...
Sarclisa EU approval

Sanofi Dupixent application for treatment of chronic spontaneous urticaria in adults, adolescents accepted for USFDA review

Ruchika Sharma7 March 2023 3:30 PM IST
Dupixent is a fully human monoclonal antibody that inhibits the signaling of the IL-4 and IL-13 pathways and is not an immunosuppressant.
Caplin Steriles gets USFDA nod for Procainamide Hydrochloride Injection for treating abnormal heart rhythm

Sanofi, Regeneron Pharma bag USFDA nod for Kevzara to treat polymyalgia rheumatica

Ruchika Sharma2 March 2023 1:15 PM IST
Polymyalgia rheumatica often initially presents with pain and stiffness around the neck, shoulder and hip area and symptoms include fatigue, low-grade...
Itepekimab met primary endpoint in one of two COPD phase 3 studies: Sanofi, Regeneron

Glooko, Sanofi collaborate for SoloStar Pen Connectivity with New Device SoloSmart

Ruchika Sharma26 Feb 2023 1:00 PM IST
Palo Alto: Glooko Inc. has announced that they have entered into a partnering agreement with Sanofi to increase their support of people living...
Itepekimab met primary endpoint in one of two COPD phase 3 studies: Sanofi, Regeneron

Sanofi gets USFDA nod for hemophilia A treatment ALTUVIIIO

Ruchika Sharma24 Feb 2023 12:19 PM IST
Hemophilia A is a rare, lifelong condition in which the ability of a person's blood to clot properly is impaired, leading to excessive bleeds and...
Johnson & Johnson names Ex-Sanofi Chief Dr John Reed as Executive Vice President, Pharmaceuticals, RnD

Johnson & Johnson names Ex-Sanofi Chief Dr John Reed as Executive Vice President, Pharmaceuticals, RnD

Ruchika Sharma14 Feb 2023 12:15 PM IST
Dr Reed previously served as Executive Vice President, Global Head of Research and Development for Sanofi and brings more than 35 years of biomedical...
Sanofi to buy Autoimmune Disease treatment from Dren Bio for up to USD 1.9 billion

Drugmaker Sanofi to let go of staff at vaccine plants in India as part of review

Ruchika Sharma31 Jan 2023 1:30 PM IST
About 800 employees could be affected by the decision, two sources familiar with the matter said.
USFDA grants priority review to Sanofi-Regeneron Dupixent for bullous pemphigoid

Sanofi Gets CDSCO panel nod to market Olipudase alfa for rare disease

Dr. Divya Colin30 Jan 2023 6:00 PM IST
New Delhi: Granting the local Phase III and phase IV clinical trial waiver in the country, the Subject Expert Committee (SEC) functional under the...
Itepekimab met primary endpoint in one of two COPD phase 3 studies: Sanofi, Regeneron

Sanofi Dupixent gets European Commission okay to treat eosinophilic esophagitis

Ruchika Sharma30 Jan 2023 4:30 PM IST
Dupixent is an injection administered under the skin (subcutaneous injection) at different injection sites.
USFDA grants priority review to Sanofi-Regeneron Dupixent for bullous pemphigoid

Sanofi Gets CDSCO Panel Nod To Market Avalglucosidase Alfa Powder for Pompe Disease

Dr. Divya Colin28 Jan 2023 6:00 PM IST
New Delhi: Granting a local Phase III and Phase IV clinical trial waiver, the Subject Expert Committee (SEC) functional under the Central Drug...
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