Tolerance and Pharmacokinetic/Pharmacokinetic Study of IBI362 15mg in Patients With Moderate to Severe Obesity
NCT07000955 · Active, not recruiting
Last updated 2026-05-28This clinical trial is testing the safety and how the body processes a 15mg dose of the drug IBI362 in adults with moderate to severe obesity.
Status Active, not recruiting Ongoing, but no longer enrolling new participants.
Phase Phase1, Phase2
Type Interventional (clinical trial)
Design Randomized, triple-blind treatment study
Participants 98 people
Who can join Ages 18–55 · all sexes
Timeline Started 2025-06 · est. completion 2027-05
Where 1 site · China
What this study is testing ClinicalTrials.gov NCT07000955 ↗
Description as written by the study sponsor.
This study is a multicenter, randomized, partially double-blind (double-blind in both the IBI362 group and the placebo group, with the tirbopeptide group open), placebo and active drug controlled design study
Treatments tested
- Tirzepatide Drug
Tirzepatide administered subcutaneously (SC) once a week.
- Placebo Drug
Placebo administered subcutaneously (SC) once a week.
- IBI362 Drug
IBI362 administered subcutaneously (SC) once a week.
| Main thing measured | The Incidence of adverse events and serious adverse events during the treatment period |
|---|---|
| Sponsor | Innovent Biologics (Suzhou) Co. Ltd. |
| Conditions studied | Obesity |
| GLP-1 drugs | — |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT07000955 ↗