Femme et Homme
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Extrait
The primary objectives of this study are to compare the safety of the combination of ABT-450/r/ABT-267 and ABT-333 administered with and without RBV for 12 weeks of treatment with ABT-450/r/ABT-267 and ABT-333 administered with and without RBV compared to the historical SVR rate of telaprevir plus pegIFN and RBV therapy in treatment-naive HCV genotype (GT) 1a-infected adults without cirrhosis.
Critère d'inclusion
- Chronic Hepatitis C Infection