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A Study of IBI362 Evaluating Weight Loss in Obese and Overweight Chinese Subjects

NCT04904913 · Completed

Last updated 2026-05-28

This clinical trial is testing the weight-loss effects of the drug IBI362 in Chinese adults who are overweight or obese.

Status Completed The study has finished.
Phase Phase 2 Tests whether it works and watches safety in a moderate group.
Type Interventional (clinical trial)
Design Randomized, double-blind treatment study
Participants 328 people
Who can join Ages 18–75 · all sexes
Timeline Started 2021-06 · est. completion 2023-12
Where 1 site · China

What this study is testing ClinicalTrials.gov NCT04904913 ↗

Description as written by the study sponsor.

This is a multicenter, double-blind, randomized, placebo-controlled study conducted in overweight or obese subjects. This study is divided into the first stage and the second stage. The participant enrollment and data analysis in the two stage are independent and do not influence each other. In the first stage of this study, about 240 subjects will be enrolled. Qualified subjects will receive placebo in a 2-week introduction period, after that, they will be randomized to IBI362 low dose, IBI362 moderate dose, IBI362 high dose groups, in every group, subjects will be randomized to IBI362 and placebo groups at a ratio of 3:1. Random stratification is performed based on BMI \< 28.0 kg/㎡ and BMI≥28.0 kg/㎡. The subjects received drug administration once weekly. The entire trial covers a 3-week screening period, a 2-week placebo introduction period, a-24 week double-blind treatment period, and a 12-week drug discontinuation follow-up period. During the entire research period, the subjects shall maintain diet and exercise control. The second stage is IBI362 extra high dose study, about 80 subjects will be enrolled. Qualified participants will receive placebo in a 2-week introduction period, after that, they will be randomized to IBI362 extra high dose and placebo groups at a ratio of 3:1. The subjects received drug administration once weekly. The entire trial covers a 3-week screening period, a 2-week placebo introduction period, a 24-week double-blind treatment period, a 24-week extended treatment period, and a 12-week drug discontinuation follow-up period. The 24-week extended treatment period is optional. During the entire research period, the subjects shall maintain diet and exercise control.

Treatments tested

Main thing measuredPercent Change from Baseline in Body Weight
SponsorInnovent Biologics (Suzhou) Co. Ltd.
Conditions studiedOverweight/ Obesity
GLP-1 drugs

Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT04904913 ↗