LivingGLP1
Study S002138

A Phase 3 Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Adult Participants With Obstructive Sleep Apnea on Positive Airway Pressure Therapy and Living With Overweight or Obesity

Registration

Registration
NCT07225686
Acronym
MARITIME-OSA-1
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
250
Start
2025-12-19
Primary completion
2027-08-20
Lead sponsor
Amgen
Conditions
Obesity; Obstructive Sleep Apnea
Interventions
DRUG:Maridebart cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Change in Apnea-Hypopnea Index (AHI) from baseline at week 52 [At week 52]

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