LivingGLP1
Study S002150

Efficacy and Safety of Semaglutide 2.4 mg Once-weekly in Asians With Obesity Diagnosed as BMI ≥ 25 kg/m2 According to Local Guidelines

Registration

Registration
NCT04998136
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
150
Start
2022-08-15
Primary completion
2023-10-16
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:Semaglutide 2.4 mg; DRUG:Placebo (semaglutide 2.4 mg)
Results posted
TRUE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1265-5285

Registered primary outcomes

  • Change in Body Weight (%) : In-trial Observation Period [Baseline (week 0), end of treatment (week 44)]
  • Change in Body Weight (%) : On-treatment Observation Period [Baseline (week 0), end of treatment (week 44)]
  • Number of Participants Achieved More Than or Equal to (≥) 5 Percent (%) Body Weight Reduction (Yes/no) : In-trial Observation Period [At week 44]
  • Number of Participants Achieved More Than or Equal to (≥) 5 Percent (%) Body Weight Reduction (Yes/no) : On-treatment Observation Period [At week 44]

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
R0016602Once-weekly semaglutide 2·4 mg in an Asian population with obesity, defined as BMI ≥25 kg/m2, in South Korea and Thailand (STEP 11): a randomised, double-blind, placebo-controlled, phase 3 trial.
Lim S, The lancet. Diabetes & endocrinology
2025Randomized trialPMID 40825340DOIcites ClinicalTrials.gov:NCT04998136; registry reference DERIVED:40825340