LivingGLP1
Study S002380

A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Adult Participants Without Type 2 Diabetes Mellitus Who Have Obesity or Are Overweight

Registration

Registration
NCT06858839
Acronym
MARITIME-1
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
3853
Start
2025-03-12
Primary completion
2027-01-21
Lead sponsor
Amgen
Conditions
Obesity
Interventions
DRUG:Maridebart Cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
EUDRACT_NUMBER:2024-515524-36

Registered primary outcomes

  • Percent Change From Baseline in Body Weight at Week 72 [Baseline and Week 72]

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.