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BOSTON, Nov. 11, 2014 /PRNewswire/ (NYSE: ABBV) today announced is a result of studies in chronic hepatitis C patients with hiv type 1 (HIV 1) co infection (TURQUOISE I) and liver transplant recipients (CORAL I) on the Liver Meeting New, detailed originates from the beginning with the Phase 2 portion of AbbVie's Phase 2/3 open label study, TURQUOISE I, showed patients co who have contracted genotype 1 (GT1) hepatitis C virus (HCV) and HIV 1 receiving AbbVie's investigational treatment and ribavirin (RBV) for 3 months or 24 weeks achieved sustained virologic response rates 12 weeks post treatment (SVR12) of 93.5 percent (n=29/31) and 90.6 % (n=29/32), respectively. "TURQUOISE I is just about the few dedicated studies looking specifically as of this population, that happen to be seen in everyday clinical practice..

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