LivingGLP1
Study S001089

Efficacy and Safety of Cagrilintide S.C. 2.4 mg in Combination With Semaglutide S.C. 2.4 mg (CagriSema S.C. 2.4 mg/2.4 mg) Once-Weekly in East Asian Participants With Overweight or Obesity

Registration

Registration
NCT05813925
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
331
Start
2023-04-03
Primary completion
2025-01-17
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity or Overweight
Interventions
DRUG:Cagrilintide; DRUG:Semaglutide; DRUG:Placebo Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1277-3764; REGISTRY:jRCT2031220734

Registered primary outcomes

  • Relative Change in Body Weight [From baseline (week 0) to end of treatment (week 68)]

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
R0007530Efficacy and safety of co-administered cagrilintide and semaglutide versus semaglutide alone in adults with overweight or obesity with or without type 2 diabetes in Japan and Taiwan (REDEFINE 5): a multicentre, randomised, active-controlled, phase 3a trial.
Yamauchi T, The lancet. Diabetes & endocrinology
2026Randomized trialPMID 42009015DOIcites ClinicalTrials.gov:NCT05813925; registry reference DERIVED:42009015