A Study of IBI362 in Participants With Type 2 Diabetes
NCT05606913 · Completed
Last updated 2026-05-28This clinical trial is testing the safety and effects of the medication IBI362 in adults with type 2 diabetes to see how it impacts blood sugar levels over 28 weeks.
Status Completed The study has finished.
Phase Phase 3 Confirms effectiveness in a large group before approval.
Type Interventional (clinical trial)
Design Randomized, double-blind treatment study
Participants 731 people
Who can join Ages 18+ · all sexes
Timeline Started 2023-01 · est. completion 2024-04
Where 1 site · China
What this study is testing ClinicalTrials.gov NCT05606913 ↗
Description as written by the study sponsor.
This trial is conducted in China. The aim of the trial is to evaluate efficacy and Safety of IBI362 Versus dulaglutide as add-on to Metformin and/or SGLT2 inhibitor or TZD in Subjects With Type 2 Diabetes.
Treatments tested
- dulaglutide Drug
Dulaglutide administered subcutaneously (SC) once a week.
- IBI362 Drug
IBI362 administered subcutaneously (SC) once a week.
| Main thing measured | HbA1c change from baseline at week 28 |
|---|---|
| Sponsor | Innovent Biologics (Suzhou) Co. Ltd. |
| Conditions studied | Type 2 Diabetes |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT05606913 ↗