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RECRUITING
NCT07908316
PHASE1

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

View on ClinicalTrials.gov

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

Interventions

DRUG

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