drugset / Trial / NCT07156539

A Phase 3 Study of HS-20094 in Patients With T2DM

NCT07156539

Phase 3 Not yet recruiting 546 enrolled Jiangsu Hansoh Pharmaceutical Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is being conducted to evaluate the efficacy and safety of HS-20094 once weekly (QW) in subjects with type 2 diabetes mellitus not adequately controlled with metformin monotherapy or in combination with SGLT2 inhibitors compared to Dulaglutide QW for 44 weeks and 52 weeks.

Timeline

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

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dulaglutide Peptide Subcutaneous
Subject Olatorepatide Protein / enzyme biologic Subcutaneous