drugset / Trial / NCT01193478
A Multiple Ascending Dose Study of GS 5885 in Previously Untreated Subjects With Genotype 1 Chronic Hepatitis C
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |