LivingGLP1
Study S000786

Efficacy and Safety of Oral Semaglutide 25 mg Once Daily in Adults With Overweight or Obesity

Registration

Registration
NCT05564117
Acronym
OASIS 4
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
307
Start
2022-10-11
Primary completion
2024-04-18
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:Semaglutide; DRUG:Placebo semaglutide
Results posted
TRUE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1271-9056; EUDRACT_NUMBER:2021-006534-40

Registered primary outcomes

  • Percentage Change in Body Weight [Baseline (week 0), end of treatment (week 64)]
  • Number of Participants Who Achieved Body Weight Reduction Greater Than or Equal to (≥) 5% (Yes/No) [At end of treatment (week 64)]

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
R0016015Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity.
Wharton S, The New England journal of medicine
2025Randomized trialPMID 40934115DOIcites ClinicalTrials.gov:NCT05564117; registry reference DERIVED:40934115