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)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ruzasvir | Other / unclassified | 60 mg | Oral |
| Subject | Uprifosbuvir | Other / unclassified | 450 mg | Oral |