LivingGLP1
Study S002805

A Randomized, Double-blind, Placebo-controlled Phase Ⅲ Clinical Study to Evaluate the Efficacy and Safety of HS-20094 in Overweight and Obese Subjects

Registration

Registration
NCT06839664
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
604
Start
2024-11-16
Primary completion
2026-01-04
Lead sponsor
Jiangsu Hansoh Pharmaceutical Co., Ltd.
Conditions
Overweight; Obesity
Interventions
DRUG:HS-20094 injection; DRUG:Placebo injection
Results posted
FALSE

Registered primary outcomes

  • Percent Change from Baseline in Body Weight [Baseline, week 48]
  • Percentage of Participants Who Achieve weight loss≥ 5% from Baseline [Baseline, week 48]

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