LivingGLP1
Study S002553

A Multi-center, Randomized, Double-blind, Placebo-controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of VCT220 Tablets in Overweight/Obese Subjects

Registration

Registration
NCT06569355
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
250
Start
2023-12-27
Primary completion
2024-07-13
Lead sponsor
Vincentage Pharma Co., Ltd
Conditions
Obesity; Overweight
Interventions
DRUG:VCT220; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Percentage change in body weight [From baseline (week 1) to week 16]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0001121Oral nonpeptide GLP-1 receptor agonist VCT220 for obesity treatment: a randomized, double-blind, phase II trial.
Ji L, Signal transduction and targeted therapy
2026Randomized trialPMID 42595749DOIcites ClinicalTrials.gov:NCT06569355; registry reference DERIVED:42595749