LivingGLP1
Study S000582

Efficacy and Safety of Oral Semaglutide 50 mg Once Daily in East Asian Participants With Overweight or Obesity

Registration

Registration
NCT05132088
Acronym
OASIS 2
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
201
Start
2021-11-16
Primary completion
2023-07-11
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight and Obesity
Interventions
DRUG:semaglutide 50 mg; DRUG:placebo (semaglutide)
Results posted
TRUE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1258-7561

Registered primary outcomes

  • Percent Change From Baseline in Body Weight [Baseline (week 0), week 68]
  • Number of Participants Who Achieved Body Weight Reduction Greater Than or Equal (>=) to 5% (Yes/No) [At week 68]

Linked records (2)

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
R0034356Perspectives and Insights on Glucagon-Like Peptide-1 Receptor Agonists: From Development to Submission of a Clinical Trial Application in Canada
Mihirkumar Patel, Zenodo (CERN European Organization for Nuclear Research)
2026Randomized trialDOIcites ClinicalTrials.gov:NCT05132088
R0006183Oral Semaglutide in an East Asian Population With Overweight or Obesity, With or Without Type 2 Diabetes: The OASIS 2 Randomized Clinical Trial.
Kadowaki T, JAMA internal medicine
2025Randomized trialPMID 40758358DOIcites ClinicalTrials.gov:NCT05132088; registry reference DERIVED:40758358