Nucleoside/nucleotide analogue polymerase inhibitors in development

Clin Liver Dis. 2013 Feb;17(1):105-10. doi: 10.1016/j.cld.2012.09.007.

Abstract

Nucleoside/nucleotide analogue polymerase inhibitors (NPIs) are analogues of natural substrates that bind the active site of NS5B and terminate viral RNA chain generation and generally provide a high genetic barrier to resistance and are effective in all genotypes. NPIs such as sofosbuvir (GS-7977) show high antiviral activities that, together with their high genetic barrier to resistance, suggest that they are optimal backbone candidates for all-oral combination therapies. Several trials are ongoing to further define the potential of all-oral regimens with sofosbuvir (GS-7977). Recent interim analyses indicate that many patients treated with only 2 direct-acting antiviral agents experience viral breakthrough, which can be significantly reduced by the addition of ribavirin without pegylated interferon α.

Publication types

  • Review

MeSH terms

  • Cytidine / analogs & derivatives
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / therapeutic use
  • Drugs, Investigational / therapeutic use
  • Enzyme Inhibitors / therapeutic use*
  • Hepacivirus / enzymology*
  • Hepatitis C / drug therapy*
  • Humans
  • Protein Conformation
  • RNA-Dependent RNA Polymerase / antagonists & inhibitors*
  • Sofosbuvir
  • Uridine Monophosphate / analogs & derivatives
  • Uridine Monophosphate / therapeutic use
  • Viral Nonstructural Proteins

Substances

  • 2'-fluoro-2'-methyl-3',5'-diisobutyryldeoxycytidine
  • Drugs, Investigational
  • Enzyme Inhibitors
  • Viral Nonstructural Proteins
  • Deoxycytidine
  • Cytidine
  • Uridine Monophosphate
  • NS-5 protein, hepatitis C virus
  • RNA-Dependent RNA Polymerase
  • Sofosbuvir