Trial intelligence / Profile preview

HRS-5817 in obesity

NCT06934408Phase 1Recruiting

Sponsor
Fujian Shengdi Pharmaceuticals
Start
May 2025
Primary completion
Apr 2027
Modality
Nucleic Acid Therapeutics, Small Molecules
Countries
1
01

Overview

Phase 1, randomised trial in obesity comparing HRS-5817 Injection Group with Placebo Group (2 arms). Primary endpoint: Adverse Events at 253 days. Started May 2025; status: recruiting.

02

Drugs

HRS-5817
03

Conditions

obesity

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