TMC647055, a potent nonnucleoside hepatitis C virus NS5B polymerase inhibitor with cross-genotypic coverage.

نویسندگان

  • Benoit Devogelaere
  • Jan Martin Berke
  • Leen Vijgen
  • Pascale Dehertogh
  • Els Fransen
  • Erna Cleiren
  • Liesbet van der Helm
  • Origène Nyanguile
  • Abdellah Tahri
  • Katie Amssoms
  • Oliver Lenz
  • Maxwell D Cummings
  • Reginald F Clayton
  • Sandrine Vendeville
  • Pierre Raboisson
  • Kenneth A Simmen
  • Gregory C Fanning
  • Tse-I Lin
چکیده

Hepatitis C virus (HCV) infection is a major global health burden and is associated with an increased risk of liver cirrhosis and hepatocellular carcinoma. There remains an unmet medical need for efficacious and safe direct antivirals with complementary modes of action for combination in treatment regimens to deliver a high cure rate with a short duration of treatment for HCV patients. Here we report the in vitro inhibitory activity, mode of action, binding kinetics, and resistance profile of TMC647055, a novel and potent nonnucleoside inhibitor of the HCV NS5B RNA-dependent RNA polymerase. In vitro combination studies with an HCV NS3/4A protease inhibitor demonstrated potent suppression of HCV RNA replication, confirming the potential for combination of these two classes in the treatment of chronic HCV infection. TMC647055 is a potent nonnucleoside NS5B polymerase inhibitor of HCV replication with a promising in vitro biochemical, kinetic, and virological profile that is currently undergoing clinical evaluation.

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عنوان ژورنال:
  • Antimicrobial agents and chemotherapy

دوره 56 9  شماره 

صفحات  -

تاریخ انتشار 2012