The FDA is set to give its decision on SNY and REGN's sBLA for Dupixent for chronic spontaneous urticaria on April 18, 2025.
Aging is undoubtedly a natural part of life, and while some embrace what time does to their skin, others might look for a ...
Paris: Sanofi and Regeneron has announced that the US Food and Drug Administration (FDA) has accepted for review the ...
Zai Lab and argenx have announced receipt of approval from the National Medical Products Administration (NMPA) of China for ...
French drug major Sanofi (SNY) and Regeneron Pharmaceuticals, Inc. (REGN) announced Friday that the U.S. Food and Drug Administration ...
SBLA’s Liquid Facelift Wand Line Relaxing Complex eliminates fine lines, deep lines, and wrinkles while visibly plumping skin, and contouring the face. After years of research and formulation ...
The resubmitted sBLA will include results from Study C, which evaluated biologic-naive patients with uncontrolled CSU on antihistamines.
US FDA accepts for review the resubmission of sBLA for Dupixent to treat chronic spontaneous urticaria: Paris Monday, November 18, 2024, 11:00 Hrs [IST] The US Food and Drug Admin ...