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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

18 states

Healthy volunteers

No

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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

Gainesville · Hialeah · Margate · Miami …

Georgia

Johns Creek · Union City · Woodstock

Idaho

Meridian

Illinois

Skokie

Louisiana

Baton Rouge

Mississippi

Ridgeland

Montana

Missoula

Nevada

Las Vegas

Source: ClinicalTrials.gov · NCT07575399 · last updated 2026-08-27

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