Entecavir: A review of its use in chronic hepatitis B

被引:26
作者
Robinson, Dean M. [1 ]
Scott, Lesley J. [1 ]
Plosker, Greg L. [1 ]
机构
[1] Adis Int Ltd, Auckland 1311, New Zealand
关键词
entecavir; hepatitis B; pharmacodynamics; pharmacokinetics; therapeutic use; tolerability;
D O I
10.2165/00003495-200666120-00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Entecavir (Baraclude (TM)) 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.
引用
收藏
页码:1605 / 1622
页数:18
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