LivingGLP1
Study S000525

A Multicenter, Randomized, Double-blind, Placebo- Parallel Controlled, Phase II Study to Evaluate the Efficacy and Safety of HRS9531 Injection in Obese Subjects Without Diabetes

Registration

Registration
NCT05881837
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
249
Start
2023-06-13
Primary completion
2024-10-13
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Overweight or Obesity
Interventions
DRUG:HRS9531 injection; DRUG:HRS9531 injection Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Percentage change in body weight [Week 0, Week 24]

Linked records (0)

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