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 Not on Positive Airway Pressure Therapy and Living With Overweight or Obesity (MARITIME-OSA-2)
Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY
This Phase 3 clinical trial is designed to evaluate the efficacy and safety of maridebart cafraglutide compared to placebo over a 52-week period in adults with obstructive sleep apnea (OSA) who are not on PAP therapy and are living with overweight or obesity.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:
• Participants must have an AHI of 15 or higher on polysomnography (PSG) at Day 1 before randomization.
• Body Mass Index (BMI) of 27 kg/m\^2 or more at the time of screening.
• History of at least one unsuccessful attempt at weight loss through diet and exercise.
• Participants must not have used PAP therapy for at least 4 weeks before screening, are unwilling/unable to use PAP, and do not plan to use PAP therapy during the study.
Locations
United States
Florida
Teradan Clinical Trials
RECRUITING
Brandon
Clinical Research Center Of Florida
RECRUITING
Pompano Beach
Ohio
CTI Clinical Research Center
RECRUITING
Cincinnati
Texas
FutureSearch Trials of Neurology
RECRUITING
Austin
Epic Medical Research - DeSoto
RECRUITING
Desoto
Washington
Northwest Clinical Research Center
RECRUITING
Bellevue
Other Locations
Canada
Aggarwal and Associates Ltd
RECRUITING
Brampton
Wharton Medical Clinic
RECRUITING
Hamilton
Contact Information
Primary
Amgen Call Center
medinfo@amgen.com
866-572-6436
Time Frame
Start Date: 2025-11-25
Estimated Completion Date: 2028-09-13
Participants
Target number of participants: 250
Treatments
Experimental: Maridebart Cafraglutide
Participants will receive maridebart cafraglutide subcutaneously (SC).
Placebo_comparator: Placebo
Participants will receive placebo SC.
Related Therapeutic Areas
Sponsors
Leads: Amgen