drugset / Trial / NCT07832799

Comparing the Extent to Which Two Maridebart Cafraglutide Drug Products Are Made Available in the Body After a Single Subcutaneous Dose

NCT07832799 ↗

Phase 1 Not yet recruiting 340 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this trial is to evaluate the pharmacokinetics (PK) of two maridebart cafraglutide drug products in participants living with overweight or obesity.

Timeline

Start
2026-10-12
Primary completion
2027-03-23
Completion
2027-03-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Maridebart Cafraglutide Unknown — Subcutaneous

Indications