LivingGLP1
Study S003338

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of VCT220 Tablets in Overweight or Obese Participants

Registration

Registration
NCT06939296
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
840
Start
2024-12-24
Primary completion
2025-11-25
Lead sponsor
Vincentage Pharma Co., Ltd
Conditions
Obesity; Overweight
Interventions
DRUG:VCT220; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Percentage change from baseline in body weight [From baseline to week 34]
  • The proportion of subjects with a body weight reduction ≥5% from baseline [From baseline to week 34]

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