drugset / Trial / NCT01523990

A Study to Evaluate the Safety, Tolerability, and PK in Healthy Volunteers and HCV Genotype 1 Infected Patients

NCT01523990

Phase 1 Completed 135 enrolled TaiGen Biotechnology Co., Ltd.
RandomizedSingle-groupQuadruple-blindTreatment

Summary

A Safety Study to Evaluate the Safety, Tolerability, and Pharmacokinetics in HCV Genotype 1 Infected Patients

Timeline

Start
2011-10
Primary completion
2012-04
Completion
2013-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Furaprevir Small molecule 50 mg Oral
Subject Furaprevir Small molecule 100 mg Oral
Subject Furaprevir Small molecule 200 mg Oral
Subject Furaprevir Small molecule 400 mg Oral
Subject Furaprevir Small molecule 600 mg Oral
Subject Furaprevir Small molecule 800 mg Oral