CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 610 enrolled
Drug / intervention
Placebo +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05607680
NCT05607680Phase 3Completed

A Randomized, Double-blind, Placebo-controlled Phase III Study Evaluating the Efficacy and Safety of IBI362 in Chinese Participants With Obesity or Overweight (GLORY-1)

Innovent Biologics (Suzhou) Co. Ltd.·interventional·Posted Nov 7, 2022·Updated Nov 12, 2024

In Brief

A Phase 3 clinical trial evaluating Placebo and IBI362 for Obesity Or Overweight. Completed, enrolled 610 participants across 23 sites.

Detailed Summary

This is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical study evaluating the efficacy and safety of IBI362 in overweight or obese subjects. Subjects will be randomly assigned to IBI362 low-dose, high-dose and placebo groups. The entire trial cycle includes a 2-week screening period, a 48-week double-blind treatment period, and a 12-week drug withdrawal follow-up period after the end of treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3CompletedFinished
2023202420252026
First PostedNov 7, 2022
Enrollment StartNov 14, 2022
Primary CompletionAug 21, 2023
Study CompletionApr 16, 2024
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 3.7 years ago

Interventions

Placebodrug

Placebo administered subcutaneously (SC) once a week.

IBI362drug

IBI362 administered subcutaneously (SC) once a week.