CSPC Pharmaceutical Group Wins FDA Nod for GLP-1/GIP Dual Agonist Clinical Trial

Reuters12-05 18:53

CSPC Pharmaceutical Group Wins FDA Nod for GLP-1/GIP Dual Agonist Clinical Trial

CSPC Pharmaceutical Group Ltd. has received approval from the U.S. Food and Drug Administration (FDA) to conduct clinical trials for its GLP-1/GIP receptor dual-biased agonist polypeptide injection, SYH2069. The clinical trial will focus on weight management for individuals with obesity or overweight and at least one weight-related comorbidity, with additional potential to improve glycemic control in adults with type 2 diabetes mellitus. The product, which has shown promising results in preclinical studies, represents a potential new-generation therapeutic agent for metabolic diseases. No other organizations were mentioned as obtaining this approval.

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. CSPC Pharmaceutical Group 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-20251205-11946576), on December 05, 2025, and is solely responsible for the information contained therein.

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