CSPC Pharmaceutical’s SYH9017 Receives NMPA Clearance for Weight Management Clinical Trial

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China-based CSPC Pharmaceutical Group Co., Ltd. (HKG: 1093) has announced clinical clearance from the National Medical Products Administration (NMPA) for its SYH9017, a biosimilar version of Denmark-based Novo Nordisk’s (NYSE: NVO) weight loss drug semaglutide (Ozempic/Wegovy). The clearance allows SYH9017 to proceed to clinical trials focused on weight management for adult overweight or obese patients, aiming to reduce calorie intake and increase physical activity.

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Semaglutide’s Therapeutic Potential and SYH9017’s Development
A glucagon-like peptide-1 (GLP-1) agonist, semaglutide was approved in China to treat type 2 diabetes in 2021 and for weight reduction in 2024. SYH9017 is the first homegrown, once-monthly semaglutide copycat to enter clinical trials in China. Pre-clinical studies have demonstrated that SYH9017 has a comparable weight loss effect to the listed semaglutide and exhibits good safety. The drug also features a significantly prolonged half-life, which supports the development of a monthly dosage form for clinical use. In addition to weight management, SYH9017 has the potential to treat type 2 diabetes and reduce the risk of cardiovascular disease.-Fineline Info & Tech

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