drugset / Trial / NCT01737684

A Single-Dose Study of the Pharmacokinetics of Vibegron (MK-4618) in Adults With Hepatic Insufficiency (MK-4618-013)

NCT01737684

Phase 1 Completed 16 enrolled Merck Sharp & Dohme LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will investigate the pharmacokinetics of a single oral dose of vibegron (MK-4618) administered to participants with moderate hepatic insufficiency and healthy participants matched for age, gender, and body mass index (BMI). Participants may be enrolled with mild hepatic insufficiency.

Timeline

Start
2013-01-15
Primary completion
2013-06-14
Completion
2013-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Vibegron Unknown 100 mg Oral

Indications