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Clinical Trial Summary

This study will explore the relationship of different DEB025 doses in combination with RBV to pharmacokinetic, pharmacodynamic (i.e. viral load reduction) and safety profiles in chronic hepatitis C GT 2 and 3 patients who have previously failed interferon therapy or are intolerant or unable to take interferon


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02094443
Study type Interventional
Source Debiopharm International SA
Contact
Status Completed
Phase Phase 2
Start date March 2014
Completion date April 2015