A Study Comparing the Efficacy and Safety of HRS9531 Injection With Semaglutide Injection in Subjects With Obesity
NCT07285902 · Active, not recruiting
Last updated 2026-05-28This clinical trial compares the effects and safety of HRS9531 injection to semaglutide injection in adults with obesity over a 52-week period.
Status Active, not recruiting Ongoing, but no longer enrolling new participants.
Phase Phase 3 Confirms effectiveness in a large group before approval.
Type Interventional (clinical trial)
Design Randomized, open-label (no blinding) treatment study
Participants 572 people
Who can join Ages 18+ · all sexes
Timeline Started 2025-12 · est. completion 2027-03
Where 2 sites · China
What this study is testing ClinicalTrials.gov NCT07285902 ↗
Description as written by the study sponsor.
This study is a multicenter, randomized, open-label, parallel-controlled, phase III study to compare the efficacy, safety, and tolerability of HRS9531 versus semaglutide once weekly (QW) in adult subjects with obesity
Treatments tested
- HRS9531 injection Drug
HRS9531 injection
- Semaglutide Injection Drug
Semaglutide Injection
| Main thing measured | Percentage change from baseline in body weight after 52 weeks of treatment |
|---|---|
| Sponsor | Fujian Shengdi Pharmaceutical Co., Ltd. |
| Conditions studied | Obesity |
| GLP-1 drugs | semaglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07285902 ↗