Efficacy, safety and tolerability of switching from GLP-1RA to maridebart cafraglutide in adults with obesity or overweight.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
300
Maridebart cafraglutide will be administered via subcutaneous (SC) injection.
Percent Change from Baseline in Body Weight at Week 68
Time frame: Week 68
Percent Change in Body Weight Prior to the Start of Weekly GLP-1RA at Week 68
Time frame: Week 68
Percentage of Participants Maintaining ≥ 80% of the Body Weight Reduction Achieved with Prior Weekly GLP-1RA Treatment at Week 68
Time frame: Week 68
Percent Maintenance of the Body Weight Reduction Achieved with Prior Weekly GLP-1RA Treatment at Week 68
Time frame: Week 68
Plasma Concentration of Maridebart Cafraglutide at Week 68
Time frame: Week 68
Number of Participants with Treatment-emergent Adverse Events and Serious Adverse Events
Time frame: Up to 84 weeks
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