Everest Medicines Limited announced that the National Medical Products Administration (NMPA) of China has approved the New Drug Application (NDA) for VELSIPITY® (etrasimod arginine tablets) for the treatment of moderately to severely active ulcerative colitis in adults. The approval covers patients who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent. This regulatory approval marks a significant step in the company's strategy to expand its autoimmune portfolio and commercial product offerings in China.
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. Everest Medicines Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260206-12017455), on February 06, 2026, and is solely responsible for the information contained therein.
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