China NMPA approves SinoMab SM17 IND for inflammatory bowel disease

Reuters

Feb 24

China NMPA approves SinoMab SM17 IND for inflammatory bowel disease

SinoMab BioScience Ltd. said China’s National Medical Products Administration has approved its Investigational New Drug $(IND)$ application for SM17 to treat inflammatory bowel disease, including Crohn’s disease and ulcerative colitis. The company said it has completed follow-up visits for a Phase I bridging study in healthy volunteers evaluating subcutaneous administration of SM17 and plans to use the data to support further clinical development, including preparation for Phase II studies.

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. SinoMab BioScience 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-20260224-12028968), on February 24, 2026, and is solely responsible for the information contained therein.

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The company said it has completed follow-up visits for a Phase I bridging study in healthy volunteers evaluating subcutaneous administration of SM17 and plans to use the data to support further clinical development, including preparation for Phase II studies.Disclaimer: This news brief was created by Public Technologies  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. 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The company said it has completed follow-up visits for a Phase I bridging study in healthy volunteers evaluating subcutaneous administration of SM17 and plans to use the data to support further clinical development, including preparation for Phase II studies.\n      \n\n\nDisclaimer: 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. SinoMab BioScience 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. 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