drugset / Trial / NCT01329913
Safety, Pharmacokinetics, and Pharmacodynamics of MK-6325 in Hepatitis C Virus (HCV) Infections (MK-6325-003)
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a 2 part study of the safety, pharmacokinetics and pharmacodynamics of MK-6325 in HCV-infected participants. Part I of the study will be for Genotype (GT) 1 HCV-infected participants who will be randomized to receive either MK-6325 or placebo. If the drug is shown to be safe and efficacious in Part I, Part II will enroll GT 3 HCV-infected participants who will be randomized to receive either MK-6325 or placebo.
Timeline
- Start
- 2011-05
- Primary completion
- 2012-04
- Completion
- 2012-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MK-6325 | Small molecule | 200 mg | Oral |
| Subject | MK-6325 | Small molecule | 400 mg | Oral |
| Subject | MK-6325 | Small molecule | 800 mg | Oral |