LivingGLP1
Study S000643

A Randomized, Double-Blind, Placebo-Controlled Phase III Clinical Study to Assess the Efficacy and Safety of IBI362 in Chinese Subjects With Moderate-to-Severe Obstructive Sleep Apnea and BMI≥28 kg/m2 (GLORY-OSA)

Registration

Registration
NCT06931028
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
TRIPLE
Status
RECRUITING
Enrollment
260
Start
2025-06-12
Primary completion
2027-05-07
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Sleep Apnea; Obstructive; Obesity
Interventions
OTHER:placebo; DRUG:IBI362
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Change from Baseline in Apnea-Hypopnea Index (AHI) [Week 48]

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