LivingGLP1
Study S000302

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase II Study to Evaluate the Efficacy and Safety of HRS9531 Injection in Obese Subjects With Obstructive Sleep Apnea (OSA)

Registration

Registration
NCT06565871
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
UNKNOWN
Enrollment
108
Start
2024-08
Primary completion
2025-12
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Weight Management
Interventions
DRUG:HRS9531 Injection; DRUG:Placebo Injection
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Percentage change from baseline in body weight [Baseline,32week]

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