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drug-drug interactions. Because ART may slow the progression of HCV-related liver disease, ART should be
considered for most HIV/HCV-coinfected patients, regardless of CD4 count. If treatment with PegIFN/RBV
alone or in combination with one of the HCV NS3/4A PIs (telaprevir or boceprevir) is initiated, the ART
regimen may need to be modified to reduce the potential for drug-drug interactions and/or drug toxicities that
may develop during the period of concurrent HIV and HCV treatment. The science of HCV drug
development is evolving rapidly. As new clinical trial data on the management of HIV/HCV-coinfected
patients with newer HCV drugs become available, the Panel will modify its recommendations accordingly.
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