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Clinical Trial Summary

The primary objective of this study is to evaluate the safety and efficacy of a Response Guided Therapy of boceprevir 800 mg dosed three times a day (TID) orally (PO) in combination with Peginterferon (either alpha 2b or alpha 2a) and Ribavirin in HIV/HCV genotype 1 infected patients that failed to previous HCV therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01718301
Study type Interventional
Source Fundacion Clinic per a la Recerca Biomédica
Contact
Status Completed
Phase Phase 3
Start date March 2013
Completion date June 2015

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