drugset / Trial / NCT01193478

A Multiple Ascending Dose Study of GS 5885 in Previously Untreated Subjects With Genotype 1 Chronic Hepatitis C

NCT01193478

Phase 1 Completed 71 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and activity of escalating, multiple, oral doses of GS-5885 in subjects with chronic genotype 1 Hepatitis C Virus (HCV) infection. Each participant in the study will be sequestered in the clinic for the initial 5 days of the study.

Timeline

Start
2010-08
Primary completion
2011-01
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ledipasvir Small molecule 3 mg Oral
Comparator Ledipasvir Small molecule 10 mg Oral
Comparator Ledipasvir Small molecule 30 mg Oral
Comparator Ledipasvir Small molecule 90 mg Oral