Comparing the Extent to Which Maridebart Cafraglutide is Made Available in the Body of Participants Living With Overweight or Obesity After Switching From Glucagon-like Peptide-1 Receptor Agonists (GLP-1RA)

Recruiting Phase 1 Interventional Study
Obesity Overweight
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Basic Science
Participants needed
180 (estimated)
Sponsor
Amgen · Industry
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About This Trial

The primary purpose of the study is to assess the pharmacokinetics of maridebart cafraglutode after switching from weekly GLP-1RA in participants living with overweight or obesity.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 18 to 70 years of age. * Body Mass Index (BMI) ≥ 25 at screening. * BMI ≥ 23 for Asian participants at screening. * Stable body weight (approximately 5% or less gain or loss) during the 4-week run-in period, unless the study doctor determines otherwise. * Stable dose of weekly…
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