Femme et Homme
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Extrait
The primary objectives of this study are to assess the efficacy by evaluating the percentage of subjects achieving a 12-week post-treatment sustained virologic failure response (SVR12) in each treatment arm and safety of ABT-493/ABT-530 plus SOF and RBV in adults with chronic HCV GT1-6 infection who previously failed HCV treatment in an AbbVie HCV clinical study, designated as an AbbVie HCV parent study.
Critère d'inclusion
- Chronic Hepatitis C Infection