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MK-5172 in Combination with MK-8742 with and without Ribavirin (RBV) in HCV patients who failed Prior pegylated interferon (peg-IFN) and RBV treatment

Mise à jour : Il y a 4 ans
Référence : EUCTR2014-000824-12

Femme et Homme

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Extrait

1. To evaluate the efficacy of MK-5172 in combination with MK-8742 as assessed by the proportion of subjects achieving SVR12 (Sustained Virologic Response 12 weeks after the end of all study therapy), defined as HCV RNA <LLOQ (either TD[u] or TND) 12 weeks after the end of all study therapy. 2. To evaluate the safety and tolerability of MK-5172 in combination with MK-8742.

Critère d'inclusion

  • Hepatitis C

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