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Clinical Trial Summary

The purpose of this study is to evaluate the effect of food on pharmacokinetics, safety and tolerability of an experimental Hepatitis C Virus (HCV) protease inhibitor with ritonavir in healthy volunteers.


Clinical Trial Description

This is an open-label, randomized, 2 cross-over period fasting and non-fasting study. ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00909311
Study type Interventional
Source Abbott
Contact
Status Completed
Phase Phase 1
Start date May 2009

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