InnoCare Pharma Ltd. has announced that it has received approval from the Center for Drug Evaluation $(CDE)$ of the China National Medical Products Administration (NMPA) to conduct a Phase II/III clinical trial of its novel TYK2 inhibitor, soficitinib (ICP-332), for the treatment of chronic spontaneous urticaria (CSU) in China. This regulatory approval allows InnoCare to advance clinical development of soficitinib, a selective TYK2 inhibitor targeting major dermatological autoimmune diseases. No other organizations are mentioned as recipients of this approval.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. InnoCare Pharma Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9604208-en) on December 18, 2025, and is solely responsible for the information contained therein.
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