LivingGLP1
Study S000503

Efficacy and Safety of Cagrilintide s.c. in Combination With Semaglutide s.c.(CagriSema s.c. 1.0 mg/1.0 mg and 1.7 mg/1.7 mg) Once-weekly in Participants With Overweight or Obesity

Registration

Registration
NCT06388187
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
300
Start
2024-06-24
Primary completion
2026-04-22
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:Cagrilintide; DRUG:Semaglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1298-3451; OTHER:2023-509273-24; NIH:2023

Registered primary outcomes

  • Relative change in body weight [From baseline (week 0) to end of treatment (week 68)]
  • Achievement of ≥5% weight reduction [From baseline (week 0) to end of treatment (week 68)]

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