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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)
Sponsor: Amgen
Summary
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.
Official title: A Phase 1, Randomized, Double-blind, Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Maridebart Cafraglutide After Switching From Glucagon-like Peptide-1 Receptor Agonists in Participants Living With Overweight or Obesity
Key Details
Gender
All
Age Range
18 Years - 70 Years
Study Type
INTERVENTIONAL
Enrollment
180
Start Date
2026-11-13
Completion Date
2028-02-25
Last Updated
2026-11-02
Healthy Volunteers
No
Conditions
Interventions
Maridebart cafraglutide
Administered subcutaneously.
Locations (9)
Arizona Research Center
Phoenix, Arizona, United States
Catalina Research Institute LLC (CRI) - Montclair
Montclair, California, United States
Fortrea Clinical Research Unit - Daytona Beach
Daytona Beach, Florida, United States
AGA Clinical Trials
Hialeah, Florida, United States
K2 Medical Research Orlando
Maitland, Florida, United States
The Alliance for Multispecialty Research - Lexington
Lexington, Kentucky, United States
Alliance for Multispecialty Research - Knoxville
Knoxville, Tennessee, United States
Fortrea Clinical Research Unit - Dallas
Dallas, Texas, United States
Fortrea Clinical Research Unit Inc. - Madison
Madison, Wisconsin, United States