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)
Part of paid clinical trials in Pelham, Alabama.
- Sponsor
- Amgen
- Study ID
- NCT07575399
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Obesity or Overweight
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Not accepted
Interventions
- Maridebart Cafraglutide — DRUGMaridebart cafraglutide will be administered via subcutaneous (SC) injection.
Study Details
Efficacy, safety and tolerability of switching from GLP-1RA to maridebart cafraglutide in adults with obesity or overweight.
Key Dates
- Start date
- May 11, 2026
- Status verified
- Jun 2026
- Primary completion
- Jan 3, 2028
- Completion
- Feb 28, 2028
Study Design
- Enrollment
- 300 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: MariTide Arm 1Participants will receive maridebart cafraglutide dosing schedule 1 during the treatment period.
- Experimental: MariTide Arm 2Participants will receive maridebart cafraglutide dosing schedule 2 during the treatment period.
Primary Outcome Measure
Percent Change from Baseline in Body Weight at Week 68 [ Time Frame: Week 68 ]
Central Contacts
- Amgen Call Center866-572-6436
Locations (39)
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