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Feld JJ et al. Treatment of HCV with ABT-450/r-ombitasvir and dasabuvir with ribavirin. N Engl J Med. 2014;370(17):1594–603. SAPPHIRE I: In this study a total of 631 previously untreated patients infected with HCV genotype 1 were randomized to receive an active regimen that consisted of ABT-450/r, ombitasvir, dasabuvir and ribavirin for group A and matching placebos for group B. SVR rates were 96.2% in group A and when genotype 1 was subtype GT1b had highest SVR rates of 98%.
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3.All patients on ART were on tenofovir/emtricitabine, 41% were on efavirenz, 27% raltegravir and 21% on rilpivirine. 100% SVR12 rates were observed in the untreated group and 100% SVR4 in the ART group. No adverse events reported thus far.
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Sulkowski M, E.J., Wyles D, Trinh R, Lalezari J, Slim J, Gathe J, Ruane PJ, Wang C, Elion R, Bredeek F, Brennan R, Blick G, Khatri A, Gibbons K, Hu YB, Fredrick L, Pilot-Matias T, Da Silva-Tillmann, McGovern BB, Campbell AL, Podsadecki T. TURQUOISE-I: safety and efficacy of ABT-450/r/ombitasvir, dasabuvir, and ribavirin in patients co-infected with hepatitis C and HIV-1. International AIDS conference, 2014. TURQUOISE-1: This study has evaluated the safety and efficacy of ABT-450 /r/ombitasvir, dasabuvir and ribavirin in HIV/HCV-1 co-infected individuals. A total number 63 individuals, majority males (92.1 %), white race (76.2), GT1a (88.9 %), 19 % had cirrhosis and a few (33.3 %) were previously treated. SVR 4 for the 12 week arm was 96.8 % and EOTR for the 24 week arms was 96.7 %. No adverse events reported thus far. ART regimen used consisted of atazanavir or raltegravir
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Sulkowski M, E.J., Wyles D, Trinh R, Lalezari J, Slim J, Gathe J, Ruane PJ, Wang C, Elion R, Bredeek F, Brennan R, Blick G, Khatri A, Gibbons K, Hu YB, Fredrick L, Pilot-Matias T, Da Silva-Tillmann, McGovern BB, Campbell AL, Podsadecki T. TURQUOISE-I: safety and efficacy of ABT-450/r/ombitasvir, dasabuvir, and ribavirin in patients co-infected with hepatitis C and HIV-1. International AIDS conference, 2014. TURQUOISE-1: This study has evaluated the safety and efficacy of ABT-450 /r/ombitasvir, dasabuvir and ribavirin in HIV/HCV-1 co-infected individuals. A total number 63 individuals, majority males (92.1 %), white race (76.2), GT1a (88.9 %), 19 % had cirrhosis and a few (33.3 %) were previously treated. SVR 4 for the 12 week arm was 96.8 % and EOTR for the 24 week arms was 96.7 %. No adverse events reported thus far. ART regimen used consisted of atazanavir or raltegravir.
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