drugset / Trial / NCT00663208

A Multiple Ascending Dose Study of Daclatasvir (BMS-790052) in Hepatitis C Virus Genotype 1 Infected Subjects

NCT00663208

Phase 2 Completed 167 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to assess the change in Hepatitis C Virus RNA during dosing with daclatasvir and during the follow-up period in subjects with chronic hepatitis C infection

Timeline

Start
2008-05
Primary completion
2009-06
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Daclatasvir Small molecule 1 mg Oral
Comparator Daclatasvir Small molecule 10 mg Oral
Comparator Daclatasvir Small molecule 30 mg Oral
Comparator Daclatasvir Small molecule 60 mg Oral
Comparator Daclatasvir Small molecule 100 mg Oral