CSPC Pharmaceutical Group Limited (CSPC Pharma) has officially initiated the Phase I clinical trial of its investigational SYH2092 injection at the first study centre in China. The trial targets adult participants with overweight or obesity and follows the Notice of Approval for Clinical Trial of Drug issued by the National Medical Products Administration in August 2026.
SYH2092 is an amylin receptor agonist engineered for enhanced target activation and extended in-vivo half-life through fatty-acid modification. Preclinical studies indicated superior receptor agonistic activity, strong weight-reduction efficacy, and prolonged maintenance of weight loss compared with other amylin analogues currently in development.
The Phase I study will assess safety, tolerability, pharmacokinetics, and pharmacodynamics after a single dose in healthy volunteers. Participant recruitment and screening are in progress.
Beyond weight management, SYH2092 is also positioned to address glycaemic control in adults with type 2 diabetes mellitus, aligning with CSPC Pharma’s strategic focus on metabolic disorders.