LivingGLP1
Study S001531

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Phase III Clinical Study to Evaluate the Efficacy and Safety of HRS9531 Tablets in Overweight or Obese Subjects

Registration

Registration
NCT07670884
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
RECRUITING
Enrollment
675
Start
2026-07-24
Primary completion
2027-10-31
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Chronic Management of Body Weight
Interventions
DRUG:HRS9531 Tablet; DRUG:HRS9531 Tablet Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Percentage change from baseline in body weight after 52 weeks of treatment [After 52 weeks of treatment.]
  • Proportion of subjects with weight loss of ≥ 5% from baseline in body weight after 52 weeks of treatment [After 52 weeks of treatment.]

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