LivingGLP1
Study S001210

Efficacy and Safety of Oral Semaglutide 50 mg Once Daily in Chinese Adults With Overweight or Obesity (OASIS 3)

Registration

Registration
NCT05890976
Acronym
OASIS 3
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
200
Start
2023-05-30
Primary completion
2025-01-16
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:Semaglutide; DRUG:Semaglutide Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1266-2400

Registered primary outcomes

  • Relative Change in Body Weight [From baseline (week 0) to end of treatment (week 44)]
  • Number of Participants Who Achieve (Yes/No): Body Weight Reduction Greater Than or Equal to 5 Percent [At end of treatment (week 44)]

Linked records (0)

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.

No records link to this registration yet.