Entecavir: a review of its use in chronic hepatitis B

Drugs. 2006;66(12):1605-22; discussion 1623-4. doi: 10.2165/00003495-200666120-00009.

Abstract

Entecavir (Baraclude) is a novel nucleoside analogue of 2'-deoxyguanosine whose intracellular triphosphate form inhibits replication of the hepatitis B virus (HBV). In large, randomised, double-blind, phase III clinical trials in patients with chronic HBV infection, oral entecavir 0.5 or 1.0mg once daily for up to 96 weeks was superior to lamivudine 100 mg/day in improving hepatic histology, normalising aminotransferase levels and suppressing viraemia to levels undetectable by polymerase chain reaction (PCR) assay in nucleoside-naive hepatitis B e antigen (HBeAg)-negative (precore or core promoter mutants) and/or HBeAg-positive patients, and in lamivudine-refractory (persistent viraemia during lamivudine therapy) HBeAg-positive patients. In addition, the tolerability profile of entecavir was generally similar to that of lamivudine. Thus, entecavir is a primary option in the treatment of chronic HBV infection in both nucleoside-naive and lamivudine-refractory patients.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Area Under Curve
  • Child
  • Guanine / analogs & derivatives*
  • Guanine / metabolism
  • Guanine / pharmacokinetics
  • Guanine / therapeutic use
  • Half-Life
  • Hepatitis B, Chronic / drug therapy*
  • Hepatitis B, Chronic / metabolism
  • Hepatitis B, Chronic / mortality
  • Humans
  • Intestinal Absorption
  • Metabolic Clearance Rate
  • Randomized Controlled Trials as Topic
  • Tissue Distribution
  • Treatment Outcome

Substances

  • entecavir
  • Guanine