- Hansoh said China’s drug regulator granted clinical trial clearance for its HS-20152 injection in paroxysmal nocturnal hemoglobinuria.
- The approval enables the company to advance an internally developed new drug candidate into clinical-stage development.
- Progress in this rare-disease indication could broaden Hansoh’s pipeline positioning in specialized therapies.
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. Hansoh Pharmaceutical Group Co. 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-20260323-12062066), on March 22, 2026, and is solely responsible for the information contained therein.