Recent Clinical Experience with Famciclovir — A ‘Third Generation’ Nucleoside Prodrug

Author:

Chakrabarty Arun12,Tyring Stephen K3,Beutner Karl1,Rauser Michael2

Affiliation:

1. Solano Research, Davis, Calif., USA

2. Department of Opthamology, Loma Linda University School of Medicine, Loma Linda, Calif., USA

3. Center for Clinical Studies, Houston, Tex., USA

Abstract

The herpesviruses continue to produce considerable morbidity in man. Once infected with herpes simplex (HSV), the virus remains dormant within the nervous system and may reactivate if provoked by stress, trauma and/or other factors. To date, there is no cure, but antiviral medication can reduce duration and severity of symptoms and prophylaxis can suppress recurrent episodes of disease. The second-generation guanosine nucleosides, acyclovir and penciclovir, are effective inhibitors with low toxicity; both, however, have relatively low oral bioavailability. Subsequently, the orally bioavailable prodrugs valaciclovir and famciclovir have been introduced. These compounds offer high oral bioavailabilty and deliver acyclovir and penciclovir, respectively, to the target cells by means of more convenient dosing schedules. This short review points to recent experience with famciclovir in the management of HSV and varicella-zoster virus.

Publisher

SAGE Publications

Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Varicella‐zoster virus‐related neurological complications: From infection to immunomodulatory therapies;Reviews in Medical Virology;2024-06-11

2. Antiviral Treatment and Prophylaxis in Immunocompromised Hosts;Management of Infections in the Immunocompromised Host;2018

3. Antiviral Drug Discovery;Drug Discovery;2013-04-09

4. Guanine-Based Nucleoside Analogs as Antiviral Agents;Bioactive Heterocyclic Compound Classes;2013-03-22

5. Glycoprotein targeted therapeutics: a new era of anti-herpes simplex virus-1 therapeutics;Reviews in Medical Virology;2013-02-26

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