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NOT YET RECRUITING
NCT07575399
PHASE3

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)

Sponsor: Amgen

View on ClinicalTrials.gov

Summary

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

Official title: 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

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2026-05-25

Completion Date

2028-02-28

Last Updated

2026-05-08

Healthy Volunteers

No

Interventions

DRUG

Maridebart Cafraglutide

Maridebart cafraglutide will be administered via subcutaneous (SC) injection.