A study to evaluate the effects of the combination of 4 oral antiviral agents for the treatment of patients infected with the Hepatitis C Virus (HCV)

Mise à jour : Il y a 4 ans
Référence : EUCTR2011-000944-43

Femme et Homme

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Extrait

To evaluate the antiviral efficacy as measured by sustained virologic response (SVR, defined as HCV RNA < LLoQ 24 weeks post-treatment) of 30 mg or 90 mg GS-5885 when given with GS-9451, tegobuvir and RBV for 12 or 24 weeks To evaluate the safety and tolerability of 30 mg or 90 mg GS-5885 when given with GS-9451, tegobuvir and RBV for 12 or 24 weeks


Critère d'inclusion

  • Genotype 1 Hepatitis C Virus Infection

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