drugset / Trial / NCT02392494
Evaluation of MK-1075 in Participants With Hepatitis C Virus (HCV) Infection (MK-1075-002)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |