LivingGLP1
Study S001828

Efficacy and Safety of HRS9531 in Overweight or Obese Participants: A Multicenter, Randomized, Double-blind, Placebo-controlled Trial

Registration

Registration
NCT06396429
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
567
Start
2024-05-13
Primary completion
2025-07-07
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Overweight or Obesity
Interventions
DRUG:HRS9531 injection; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Percentage change from baseline in weight after 48 weeks of treatment [Baseline, Week 48]
  • Proportion of subjects with weight loss of≥5% from baseline after 48 weeks of treatment [Week 48]

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