- SinoMab reported clinical topline results for SM17 in moderate-to-severe atopic dermatitis, positioning the program for a potential phase 2 start as early as mid-2026.
- The company said the results support differentiation in itch relief and skin recovery versus IL-4/IL-13 biologics, while also citing a safety profile that may broaden patient eligibility compared with JAK inhibitors.
- An IND for SM17 in inflammatory bowel disease was accepted by China’s drug review center and later approved, expanding the asset’s commercial scope beyond dermatology.
- Funding raised via share subscriptions totaled HKD 493.7 million, which the company said supports continued clinical development and commercialization preparations.
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-20260323-12063745), on March 23, 2026, and is solely responsible for the information contained therein.