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AbbVie Demonstrates 96 percent SVR(12) in its Phase III Study of Treatment-Experienced Patients with Genotype 1 Hepatitis C

  • ABT-333
  • 12 weeksPEARL-III

    GT1b, treatment-naive

    (400 a)

  • ABT-450/r +ABT-267
  • ABT-333
  • Ribavirin
  • 12 weeks

  • ABT-450/r +ABT-267
  • ABT-333
  • Placebo
  • 12 weeksPEARL-IV

    GT1a, treatment-naive

    (300 a)

  • ABT-450/r +ABT-267
  • ABT-333
  • Ribavirin
  • 12 weeks

  • ABT-450/r +ABT-267
  • ABT-333
  • Placebo
  • 12 weeksTURQUOISE-II

    GT1, treatment-naive and treatment-experienced (with compensated cirrhosis)

    (380 a)

  • ABT-450/r +ABT-267
  • ABT-333
  • Ribavirin
  • 12 weeks

  • ABT-450/r +ABT-267
  • ABT-333
  • Ribavirin
  • 24 weeksa projected study population

    b ABT-450/ritonavir

    c ABT-267 is co-formulated with ABT-450/r, administered as two pills once daily

    The 3D regimen consists of boosted protease inhibitor ABT-450/ritonavir, NS5A inhibitor ABT-267, and non-nucleoside polymerase inhibitor ABT-333. The combination of three different mechanisms of action interrupts the HCV replication process with the goal of optimizing SVR rates across different patient populations. In May of 2013, AbbVie's investigational 3D regimen with and without ribavirin for HCV GT1 was designated as a Breakthrough Therapy by the U.S. Food and Drug Administration (FDA).

    ABT-450 was discovered during the ongoing collaboration between AbbVie and Enanta Pharmaceuticals (NASDAQ: ENTA) for HCV protease inhibitors and regimens that include protease inhibitors. ABT-450 is being developed by AbbVie for use in combination with AbbVie's other investigational medicines for the treatment of HCV.

    Safety Information for Ribavirin and RitonavirRibavirin and ritonavir are not approved for the investigational use discussed above, and no conclusions can or should be drawn regarding the safety or ef

    SOURCE AbbVie Inc.
    Copyright©2012 PR Newswire.
    All rights reserved

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