drugset / Trial / NCT00998985

A Study of Grazoprevir (MK-5172) in Hepatitis C-Infected Male Participants (MK-5172-004)

NCT00998985

Phase 1 Completed 91 enrolled Merck Sharp & Dohme LLC
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

EvaluationDrugModalityDoseRoute
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