drugset / Trial / NCT00998985
A Study of Grazoprevir (MK-5172) in Hepatitis C-Infected Male Participants (MK-5172-004)
RandomizedParallel-groupDouble-blindTreatment
Summary
This multiple dose study will assess the safety, tolerability, pharmacokinetics and pharmacodynamics of grazoprevir (MK-5172) in Genotype (GT) 1 and GT3 Hepatitis C virus (HCV)- infected participants. The primary hypothesis is that administration of grazoprevir for 7 days is sufficiently safe and well tolerated in HCV-infected males.
Timeline
- Start
- 2010-02-23
- Primary completion
- 2012-11-08
- Completion
- 2012-11-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 10 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 30 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 50 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 100 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 200 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 400 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 600 mg | Oral |
| Subject | GRAZOPREVIR ANHYDROUS | Small molecule | 800 mg | Oral |