TTrialPathMatch Me to Trials
← Back to trials
RecruitingObesity or Overweight

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)

Eligible age

18–99 yrs

Accepts

All genders

Locations

16 states

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

Efficacy, safety and tolerability of switching from GLP-1RA to maridebart cafraglutide in adults with obesity or overweight.

Sponsor: Amgen

You may qualify if…

  • 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.

You may not qualify if…

  • 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.

Where it's recruiting

Alabama

Pelham

Arizona

Chandler · Sun City

California

Palm Springs · Rialto · Rolling Hills Estates · San Diego

Florida

Hialeah · Margate · Miami · Orlando

Georgia

Johns Creek · Union City · Woodstock

Idaho

Meridian

Illinois

Skokie

Mississippi

Ridgeland

Nevada

Las Vegas

New York

Rochester

North Carolina

Morehead City · Raleigh · Wilmington

Source: ClinicalTrials.gov · NCT07575399 · last updated 2026-06-11

Efficacy, Safety and Tolerability of Switching From Glucagon-like Pept · TrialPath