drugset / Trial / NCT06839664

A Study of HS-20094 in Chinese Adults With Overweight or Obesity

NCT06839664 ↗

Phase 3 Completed 604 enrolled Jiangsu Hansoh Pharmaceutical Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to assess the Efficacy and safety of HS-20094 in overweight and obese patients. The study will last up to approximately 52 weeks.

Timeline

Start
2024-11-16
Primary completion
2026-01-04
Completion
2026-01-30

Outcome

Met primary endpoint

release “In March 2026, the first Phase Ⅲ clinical study (HS-20094-301) of Olatorepatide in Chinese adults with obesity or overweight met its primary endpoint:” hspharm.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject HS-20094 Unknown 5 mg Subcutaneous
Subject HS-20094 Unknown 10 mg Subcutaneous
Subject HS-20094 Unknown 15 mg Subcutaneous

Indications