drugset / Trial / NCT07690826

A Study to Evaluate the Efficacy and Safety of HRS-4729 Injection in Obesity

NCT07690826

Phase 2 Not yet recruiting 252 enrolled Fujian Shengdi Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled Phase II study to evaluate the efficacy and safety of once-weekly HRS-4729 injection in adults with obesity without diabetes. Approximately 252 participants will be enrolled. The primary endpoint is percent change in body weight from baseline at Week 32 versus placebo.

Timeline

Start
2026-07
Primary completion
2027-03
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS-4729 Unknown Other

Indications