drugset / Trial / NCT07156500

A Phase 3 Study of HS-20094 in Patients With T2DM Inadequately Controlled With Diet and Exercise Alone

NCT07156500

Phase 3 Not yet recruiting 204 enrolled Jiangsu Hansoh Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical study to evaluate the efficacy and safety of HS-20094 injection in subjects with type 2 diabetes who have inadequate glycemic control with diet and exercise alone. The primary objective of this study is to evaluate the effectiveness of HS-20094 compared to placebo in controlling blood glucose levels after 44 weeks and 52 weeks treatment.

Timeline

Start
2025-09-30
Primary completion
2027-03-30
Completion
2027-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Olatorepatide Protein / enzyme biologic Subcutaneous