CSPC Pharmaceutical Group Limited announced that the National Medical Products Administration (NMPA) of China has accepted its second marketing authorisation application for Semaglutide Injection. This application, developed by CSPC Baike (Shandong) Biopharmaceutical Co., Ltd., a subsidiary of CSPC, is for the indication of long-term weight management in overweight or obese adults, alongside diet and increased physical activity. Previously, the NMPA had accepted an application for the product's use in glycemic control for adults with type 2 diabetes in August 2025. The latest application is supported by Phase III clinical trial results demonstrating significant weight reduction and improvements in metabolic markers, with efficacy and safety comparable to Novo Nordisk's semaglutide.
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