Hansoh Pharmaceutical Group Company Limited has obtained two Clinical Trial Approvals from China’s National Medical Products Administration (NMPA) for its Class 1 self-developed innovative drug, HS-20136-2 injection.
The approvals authorise separate clinical studies targeting:
1. Treatment of type 2 diabetes mellitus.
2. Weight management applications.
The Board, chaired by Ms. Zhong Huijuan, disclosed the regulatory milestone on 2 July 2026. These clearances enable Hansoh Pharmaceutical to advance HS-20136-2 through formal clinical evaluation in mainland China, marking a new phase in the Group’s R&D pipeline.
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