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Trials / Completed

CompletedNCT01431898

Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-9669 in Subjects With Chronic Hepatitis C Virus Infection

A Phase 1b, Randomized, Single-Blind, Multiple-Dose Ranging Study Evaluating the Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-9669 in Subjects With Chronic Hepatitis C Virus Infection

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
82 (actual)
Sponsor
Gilead Sciences · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This is a research study to evaluate the safety, tolerability and anti-viral activity of GS-9669 in patients with Hepatitis C infection.

Conditions

Interventions

TypeNameDescription
DRUGGS-9669 tablets
DRUGPlacebo to Match GS-9669 tablet

Timeline

Start date
2011-09-01
Primary completion
2011-12-01
Completion
2012-05-01
First posted
2011-09-12
Last updated
2012-07-25

Locations

11 sites across 2 countries: United States, Puerto Rico

Source: ClinicalTrials.gov record NCT01431898. Inclusion in this directory is not an endorsement.

Safety, Tolerability, Pharmacokinetics and Antiviral Activity of GS-9669 in Subjects With Chronic Hepatitis C Virus Infe (NCT01431898) · Clinical Trials Directory