LivingGLP1
Study S001192

A Randomised, Double-blind, Placebo-controlled Trial to Assess Safety, Tolerability and Pharmacokinetics of IBI362 in Chinese Obese Adolescent Subjects

Registration

Registration
NCT06536023
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
36
Start
2024-08-30
Primary completion
2025-07-22
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Adolescents With Obesity
Interventions
DRUG:IBI362; DRUG:IBI362 placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Incidence of adverse events and serious adverse events [up to week 20]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R00547801133-OR: Safety, Tolerability, and Pharmacokinetics of Once-Weekly Mazdutide in Chinese Adolescents with Obesity: A Phase 1b Trial
CHUNXIU GONG, Diabetes
2026Randomized trialDOIcites ClinicalTrials.gov:NCT06536023