drugset / Trial / NCT07313761

A Trial to Compare the Extent to Which Maridebart Cafraglutide (AMG 133) is Made Available in the Body When Administered Using Two Subcutaneous Presentations

NCT07313761

Phase 1 Completed 349 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The main objective of this trial is to evaluate the pharmacokinetics (PK) of maridebart cafraglutide administered as a single dose using two different SC presentations in participants living with overweight or obesity.

Timeline

Start
2025-12-15
Primary completion
2026-06-26
Completion
2026-06-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Maridebart Cafraglutide Unknown Subcutaneous

Indications

No indication recorded.