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BOCEPREVIR

Pathology : Infectious Diseases
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Study Title

Using Boceprevir (Victrelis ®) for patients who are co-infected with "HCV genotype 1 and HIV-1"

Study Detail

Study Objective

Control of viral replication (multiplication) for HCV genotype 1 for patients co-infected with HIV-1.
Monitor possible side effects of Boceprevir in combination with standard therapy.

 

Participation conditions

Inclusion criteria

• Being co-infected with HIV-1 and HCV genotype 1
• Being stable (viral replication should be controlled: undetectable viral load) for HIV
• Being at least at the second stage of fibrosis (F2) in the context of HCV genotype 1 infection.
• Being an adult (18 years old at least)

Exclusion criteria

• Being  an active addict
• Having one of the following three molecules in the regime against HIV-1: stavudine, zidovudine and didanosine.
• Being pregnant
• Feeding

Centers

Centre Hospitalier de Luxembourg

Contact person

Charlotte Lieunard
charlotte.lieunard@crp-sante.lu
+352 26 970 847

Tags: HCV genotype 1, HIV-1, Boceprevir

Studies overview

This page provides the list of clinical studies currently registered in the LuxCLIN platform in the different therapeutic areas. By clicking on each study title, more information is displayed concerning the study objective and the participation conditions.