MK-5172 in Combination with MK-8742 in Treatment-Naïve Subjects

Update Il y a 4 ans
Reference: EUCTR2014-000137-22

Woman and Man

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Extract

•To evaluate the efficacy of MK-5172 in combination with MK-8742 as assessed by the proportion of subjects in the immediate treatment arm 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. •To evaluate the safety and tolerability of MK-5172 in combination with MK-8742.


Inclusion criteria

  • Hepatitis C