drugset / Trial / NCT06482112

Alternate Dosing Study of MK-6024 in Adults With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) (MK-6024-016)

NCT06482112

Phase 2 Completed 124 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the effect of efinopegdutide administration once every 2 weeks (Q2W) versus once weekly (Q1W) on mean relative reduction from baseline in liver fat content (LFC) after 28 weeks, as well as the safety and tolerability of the different regimens of efinopegdutide.

Timeline

Start
2024-07-29
Primary completion
2025-06-27
Completion
2025-06-27

Drugs

EvaluationDrugModalityDoseRoute
Subject JNJ-64565111 Unknown 10 mg Subcutaneous
Subject JNJ-64565111 Unknown 15 mg Subcutaneous

Indications