LivingGLP1
Study S002125

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 Chinese Participants With Overweight or Obesity

Registration

Registration
NCT05996848
Acronym
REDEFINE 6
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
300
Start
2023-08-15
Primary completion
2025-01-06
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity or Overweight
Interventions
DRUG:Cagrilintide; DRUG:Semaglutide; DRUG:Placebo Semaglutide; DRUG:Placebo Cagrilintide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1267-4364

Registered primary outcomes

  • CagriSema 2.4 mg/2.4 mg versus placebo: Relative change in body weight [From baseline (week 0) to end of treatment (week 44)]
  • CagriSema 2.4 mg/2.4 mg versus placebo: Number of participants who achieve (yes/no): Body weight reduction greater than or equal to 5% [From baseline (week 0) to end of treatment (week 44)]

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