LivingGLP1
Study S000295

A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Adult Participants in Japan Who Have Obesity Disease (MARITIME 3-J)

Registration

Registration
NCT06987695
Acronym
MARITIME-3-J
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
279
Start
2025-06-13
Primary completion
2027-04-27
Lead sponsor
Amgen
Conditions
Obesity Disease
Interventions
DRUG:Maridebart cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Percent Change From Baseline in Body Weight at Week 72 [Baseline and Week 72]
  • Participants Achieving ≥ 5% Reduction in Body Weight From Baseline at Week 72 [Baseline and Week 72]

Linked records (0)

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