drugset / Trial / NCT02666352

A Study of the Pharmacokinetics of Uprifosbuvir (MK-3682) and Ruzasvir (MK-8408) in Participants With Moderate and Severe Hepatic Insufficiency (MK-3682-029)

NCT02666352

Phase 1 Completed 24 enrolled Merck Sharp & Dohme LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a non-randomized, open-label, single-dose study to evaluate the pharmacokinetics (PK) of uprifosbuvir (MK-3682), the M5 and M6 metabolites of uprifosbuvir, and ruzasvir (MK-8408), in participants with moderate hepatic insufficiency (HI), participants with severe HI, and age-matched healthy control participants.

Timeline

Start
2016-01-22
Primary completion
2017-01-16
Completion
2017-01-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Ruzasvir Other / unclassified 60 mg Oral
Subject Uprifosbuvir Other / unclassified 450 mg Oral