LivingGLP1
Study S001441

A Multicenter, Randomized, Double-blind, Placebo- Parallel Controlled, Phase II Study to Evaluate the Efficacy and Safety of HRS9531 Tablet in Obese Subjects

Registration

Registration
NCT06841445
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
166
Start
2025-04-07
Primary completion
2026-01-08
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 26 weeks of treatment [after 26 weeks of treatment]

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