drugset / Trial / NCT07226778

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

NCT07226778

Phase 1 Completed 348 enrolled Amgen
RandomizedParallel-groupOpen-labelBasic science

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
2025-10-10
Primary completion
2026-05-28
Completion
2026-05-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Maridebart Cafraglutide Unknown Subcutaneous

Indications