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New data suggests interferon-free therapy around the corner for HCV patients
Date:4/19/2012

A, et al 'ALISPORIVIR (ALV) plus PEG-INTERFERON/RIBAVIRIN (PR) in HCV G1 treatment-experienced patients achieves primary endpoint with superior efficacy at treatment week 12 compared to retreatment with PR'.
  • In Pawlotsky J-M, et al, 88% of treatment-nave HCV GT2 or 3 patients achieved SVR 12 after treatment with Alisporivir and RBV. In Alberti A, et al, 70% of null non-responders achieved cEVR when treated with Alisporivir, IFN and RBV.

    AI444040

    • Sulkowski M, et al 'Potent viral suppression with all-oral combination of DACLATASVIR (ns5a inhibitor) and GS-7977 (ns5b inhibitor), +/-RIBAVIRIN, in treatment-nave patients with chronic HCV GT1, 2, or 3'
    • Treatment-nave HCV GT1, 2, and 3 patients given an IFN- and RBV-free once-daily combination of DACLATASVIR and GS-7977 for 24 weeks achieved high rates of early virologic response (HCV RNA detectable at week 4 but undetectable at week 12 EVR) by mITT analysis: 97% EVR in GT1, 90% in GT2 and 3.

    The combination of PegIFN-α and ribavirin (RBV) is the current standard of care for chronic HCV(7), but is associated with a number of side effects including flu-like symptoms, psychiatric manifestations, autoimmune reactions, and hematologic toxicities.(8,9) Between 20-40% of patients require a dose reduction or temporary interruption in their PegIFN-α and ribavirin (RBV) treatment(10) and in 10-14% of patients, side effects are so severe that treatment must be discontinued.(8,9)

    However, studies have shown that achieving a virologic response in chronic HCV is much more dependent on the dose of IFN-α(11)/PegIFN-α(12,13,14) than RBV(15,16,17,11,18). As such, PegIFN-α free therapy is highly anticipated by healthcare professionals and patients alike.

    EASL's Secretary General Professor Mark Thursz commented on the exciting new data being showcased at the congress: "In the future, patients can look forward to all oral treatment regime
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  • Contact: Travis Taylor
    easlpressoffice@cohnwolfe.com
    44-789-438-6428
    European Association for the Study of the Liver
    Source:Eurekalert

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