Zanamivir: from drug design to the clinic

Philos Trans R Soc Lond B Biol Sci. 2001 Dec 29;356(1416):1885-93. doi: 10.1098/rstb.2001.1021.

Abstract

The development of the neuraminidase inhibitors has revolutionized the management options for influenza. Zanamivir was the first such inhibitor to be approved for the treatment of influenza in humans. It is delivered by inhalation to the respiratory tract, which is the site of viral replication, in order to ensure immediate antiviral activity. Early treatment with zanamivir in clinical trials rapidly reduced the severity and duration of influenza symptoms and associated complications. Furthermore, chemoprophylaxis with zanamivir was shown to be effective in the prevention of influenza illness. To date, there is no evidence for the emergence of clinically significant zanamivir-resistant isolates. In conclusion, zanamivir offers a useful complementary strategy to vaccination in the effective management of influenza.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / pharmacokinetics
  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use*
  • Chemoprevention / methods
  • Clinical Trials as Topic
  • Drug Design
  • Drug Interactions
  • Drug Resistance, Multiple, Viral
  • Enzyme Inhibitors / pharmacokinetics
  • Enzyme Inhibitors / pharmacology
  • Enzyme Inhibitors / therapeutic use
  • Guanidines
  • Humans
  • Influenza A virus / drug effects
  • Influenza B virus / drug effects
  • Influenza, Human / drug therapy
  • Influenza, Human / prevention & control
  • Neuraminidase / antagonists & inhibitors
  • Pyrans
  • Sialic Acids / pharmacokinetics
  • Sialic Acids / pharmacology*
  • Sialic Acids / therapeutic use*
  • Zanamivir

Substances

  • Antiviral Agents
  • Enzyme Inhibitors
  • Guanidines
  • Pyrans
  • Sialic Acids
  • Neuraminidase
  • Zanamivir