drugset / Trial / NCT02392494

Evaluation of MK-1075 in Participants With Hepatitis C Virus (HCV) Infection (MK-1075-002)

NCT02392494 ↗

Phase 1 Completed 9 enrolled Merck Sharp & Dohme LLC
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and pharmacokinetics of MK-1075, and to determine the ability of MK-1075 to reduce HCV viral load, following administration of a single dose in HCV-infected participants.

Timeline

Start
2015-04-28
Primary completion
2015-08-10
Completion
2015-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-1075 Unknown 100 mg Oral
Subject MK-1075 Unknown 200 mg Oral
Subject MK-1075 Unknown 400 mg Oral
Subject MK-1075 Unknown 800 mg Oral