drugset / Trial / NCT00895102

Bioavailability of ABT-333 Tablet Versus First in Human (FIH) Capsule Formulation and Safety, Tolerability and PK Study of Single Doses of ABT-333 in Healthy Volunteers

NCT00895102

Phase 1 Completed 34 enrolled Abbott
RandomizedCrossoverQuadruple-blind

Summary

The purpose of this study is to determine the bioavailability, pharmacokinetic and safety profiles of an experimental Hepatitis C virus (HCV) polymerase inhibitor in healthy volunteers.

Timeline

Start
2009-04
Primary completion
2009-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator dasabuvir Small molecule 400 mg
Comparator dasabuvir Small molecule 1200 mg
Comparator dasabuvir Small molecule 1600 mg
Comparator dasabuvir Small molecule 2400 mg