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Efficacy, Safety and Tolerability of Switching From Glucagon-like Peptide-1 Receptor Agonists (GLP-1RA) to Maridebart Cafraglutide in Adults With Obesity or Overweight (MARITIME-SWITCH)
RecruitingPhase 3
A Phase 3, Open-label Trial to Evaluate the Efficacy, Safety and Tolerability of Switching From the Glucagon-like Peptide-1 Receptor Agonists to Maridebart Cafraglutide in Adult Participants With Obesity or Overweight
Who can join
Ages 18 to 99 · All sexes
Full eligibility criteria
Inclusion Criteria:
* Body Mass Index (BMI) ≥ 25 at screening.
* Weight loss of ≥ 10% on weekly GLP-1 RA.
* Stable body weight.
* Stable dose of GLP-1RA.
* Stable gastrointestinal (GI) tolerability.
* Contraception for females.
* Willingness to follow trial procedures for the duration of the trial.
Exclusion Criteria:
* Obesity induced by other endocrine disorders (ex: Cushing's syndrome).
* Previous or planned surgical, endoscopic or device-based treatment for obesity.
* History of malignancy.
* Type 1/Type 2 diabetes mellitus (DM).
* Family or personal history of medullary thyroid cancer.
* Previous participation in a Maridebart Cafraglutide trial.
About the study
Efficacy, safety and tolerability of switching from GLP-1RA to maridebart cafraglutide in adults with obesity or overweight.
What is being tested
- Maridebart Cafraglutide (drug)
Sponsor: Amgen · Participants: 300 · Started: May 11, 2026
Contact the study team
Official record on ClinicalTrials.gov — NCT07575399
Locations in the U.S.
| Alabama | Cahaba Research, Inc., Pelham |
| Arizona | Arizona Clinical Trials, Chandler Epic Medical Research - Sun City, Sun City |
| California | Desert Oasis Healthcare Medical Group, Palm Springs Inland Empire Liver Foundation, Rialto Peninsula Research Associates, Rolling Hills Estates Apex Clinical Research, San Diego Southern California Clinical Research, Santa Ana |
| Florida | University of Florida Department of Medicine, Gainesville Aga Clinical Trials, Hialeah South Florida Clinical Research, Margate New Horizon Research Center, Miami Research Institute of South Florida, Miami Clinical Neuroscience Solutions, Orlando Florida Institute for Clinical Research, Orlando Progressive Medical Research, Port Orange Charter Research - The Villages, The Villages |
| Georgia | Nsc Research, Johns Creek Rophe Adult and Pediatric Medicine/Sky Clinical Research Network Group, Union City North Georgia Clinical Research, Woodstock |
| Idaho | Solaris Clinical Research, Meridian |
| Illinois | Endeavor Health, Skokie |
| Louisiana | Pennington Biomedical Research Center, Baton Rouge |
| Michigan | Arcturus Healthcare, Public Limited Company, Troy Internal Medicine Research Division, Troy |
| Mississippi | Sky Integrative Medical Center, Ridgeland |
| Montana | Montana Medical Research, Missoula |
| Nevada | Excel Clinical Research, Las Vegas |
| New York | Icahn School of Medicine at Mount Sinai, New York Rochester Clinical Research, Rochester |
| North Carolina | Centricity Research Morehead City Specialty, Morehead City Accellacare of Raleigh, Raleigh Accellacare Research of Wilmington, Wilmington |
| Oklahoma | Epic Medical Research - Oklahoma, Chickasha Lynn Health Science Institute, Oklahoma City |
| Pennsylvania | Altoona Center for Clinical Research, Duncansville |
| Texas | Epic Medical Research - DeSoto, DeSoto South Texas Research Institute, Edinburg Biopharma Informatic, LLC, Houston Research Physicians Network, LLC, Houston Texas Institute of Cardiology, McKinney North Hills Medical Research, North Richland Hills VIP Trials, San Antonio Northwest Houston Heart Center, Tomball |
| Washington | Eastside Research Associates Health Research, Redmond |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.