Valaciclovir

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Valaciclovir
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Clinical data
Trade namesValtrex, Zelitrex, others
Other namesTemplate:Infobox drug/localINNvariants
AHFS/Drugs.comMonograph
MedlinePlusa695010
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Pregnancy
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  • AU: B3
Routes of
administration		By mouth
Drug classAntiviral
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Legal status
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Pharmacokinetic data
Bioavailability55%
Protein binding13–18%
MetabolismLiver (to aciclovir)
Elimination half-life<30 minutes (valaciclovir);
2.5–3.6 hours (aciclovir)
ExcretionKidney 40–50% (aciclovir),
faecal 47% (aciclovir)
Identifiers
  • 2-[(2-Amino-6-oxo-1H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate
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Chemical and physical data
FormulaC13H20N6O4
Molar mass324.341 g·mol−1
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Data page
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Valaciclovir, also spelled valacyclovir, is an antiviral medication used to treat outbreaks of herpes simplex or herpes zoster (shingles).[2] It is also used to prevent cytomegalovirus following a kidney transplant in high risk cases.[2] It is taken by mouth.[2]

Common side effects include headache and vomiting.[2] Severe side effects may include kidney problems.[2] Use in pregnancy appears to be safe.[2] It is a prodrug, which works after being converted to aciclovir in a person's body.[2]

Valaciclovir was patented in 1987 and came into medical use in 1995.[3][4] Valaciclovir is a therapeutic alternative on the World Health Organization's List of Essential Medicines.[5] It is available as a generic medication.[6] In 2023, it was the 98th most commonly prescribed medication in the United States, with more than 7 million prescriptions.[7][8]

Medical uses

File:Valtrex pill.jpg
Valtrex brand valaciclovir 500mg tablets

Valaciclovir is used for the treatment of HSV and VZV infections, including:[9]

  • Oral and genital herpes simplex (treatment and prevention)
  • Reduction of HSV transmission from people with recurrent infection to uninfected individuals
  • Herpes zoster (shingles): the typical dosage for treatment of herpes is 1,000 mg orally three times a day for seven consecutive days.[10]
  • Prevention of cytomegalovirus following organ transplantation
  • Prevention of herpesviruses in immunocompromised people (such as those undergoing cancer chemotherapy)[11]
  • Chickenpox in children (ages 2–18)[1]

It has shown promise as a treatment for infectious mononucleosis[12][13][14] and is preventively administered in suspected cases of herpes B virus exposure.[15]

Bell's palsy does not seem to benefit from using valaciclovir as its only treatment.[16][17]

Adverse effects

Common adverse drug reactions (≥1% of people) associated with valaciclovir are the same as for aciclovir, its active metabolite. They include: nausea, vomiting, diarrhea and headache. Infrequent adverse effects (0.1–1% of patients) include: agitation, vertigo, confusion, dizziness, edema, arthralgia, sore throat, constipation, abdominal pain, rash, weakness and/or renal impairment. Rare adverse effects (<0.1% of patients) include: coma, seizures, neutropenia, leukopenia, tremor, ataxia, encephalopathy, psychotic symptoms, crystalluria, anorexia, fatigue, hepatitis, Stevens–Johnson syndrome, toxic epidermal necrolysis and/or anaphylaxis.[9]

Pharmacology

Valaciclovir is a prodrug, an esterified version of aciclovir that has greater oral bioavailability (about 55%) than aciclovir.[1] It is converted by esterases to the active drug, aciclovir, and the amino acid valine via hepatic first-pass metabolism. Aciclovir is selectively converted into a monophosphate form by viral thymidine kinase, which is more effective (3000 times) in phosphorylation of aciclovir than cellular thymidine kinase. Subsequently, the monophosphate form is further phosphorylated into a disphosphate by cellular guanylate kinase and then into the active triphosphate form, aciclo-GTP, by cellular kinases.[1]

Mechanism of action

Aciclo-GTP, the active triphosphate metabolite of aciclovir, is a very potent inhibitor of viral DNA replication. Aciclo-GTP competitively inhibits and inactivates the viral DNA polymerase.[1] Its monophosphate form also incorporates into the viral DNA, resulting in chain termination. It has also been shown that the viral enzymes cannot remove aciclo-GMP from the chain, which results in inhibition of further activity of DNA polymerase. Aciclo-GTP is fairly rapidly metabolized within the cell, possibly by cellular phosphatases.[18]

Aciclovir is active against most species in the herpesvirus family. In descending order of activity:[19]

The drug is predominantly active against HSV and, to a lesser extent, VZV. It is only of limited efficacy against EBV and CMV. However, valaciclovir has been shown to lower or eliminate the presence of the Epstein–Barr virus in subjects afflicted with acute mononucleosis, leading to a significant decrease in the severity of symptoms.[12][13][14] Valaciclovir and acyclovir act by inhibiting viral DNA replication, but as of 2016 there was little evidence that they are effective against Epstein–Barr virus.[20] Acyclovir therapy does prevent viral latency, but has not proven effective at eradicating latent viruses in nerve ganglia.[19]

As of 2005, resistance to valaciclovir has not been significant. Mechanisms of resistance in HSV include deficient viral thymidine kinase and mutations to viral thymidine kinase and/or DNA polymerase that alter substrate sensitivity.[21]

It also is used for herpes B virus postexposure prophylaxis.[15][22]

Chemistry

Details of the synthesis of valaciclovir were first published by scientists from the Wellcome Foundation.

File:Valaciclovir sythesis.svg

Aciclovir was esterified with a carboxybenzyl protected valine, using dicyclohexylcarbodiimide as the dehydrating agent. In the final step, the protecting group was removed by hydrogenation using a palladium on alumina catalyst.[23][24]

History

Valaciclovir was patented in 1987 and came into medical use in 1995.[3][4] It is available as a generic medication.[6] In 2022, it was the 113th most commonly prescribed medication in the United States, with more than 5 million prescriptions.[25][8]

Society and culture

Brand names

It is marketed by GlaxoSmithKline under the brand names Valtrex[1] and Zelitrex. Valaciclovir has been available as a generic drug in the US since November 2009.[26]

References

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  1. ^ a b c d e f Page Module:Citation/CS1/styles.css has no content."Valtrex- valacyclovir hydrochloride tablet, film coated". DailyMed. 14 June 2021. Retrieved 22 May 2022.
  2. ^ a b c d e f g Page Module:Citation/CS1/styles.css has no content."Valacyclovir Hydrochloride Monograph for Professionals". Drugs.com. American Society of Health-System Pharmacists. Retrieved 17 March 2019.
  3. ^ a b Page Module:Citation/CS1/styles.css has no content.Long SS, Pickering LK, Prober CG (2012). Principles and Practice of Pediatric Infectious Disease. Elsevier Health Sciences. p. 1502. ISBN 978-1-4377-2702-9.
  4. ^ a b Page Module:Citation/CS1/styles.css has no content.Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 504. ISBN 978-3-527-60749-5.
  5. ^ Page Module:Citation/CS1/styles.css has no content.World Health Organization (2025). The selection and use of essential medicines, 2025: WHO Model List of Essential Medicines, 24th list. Geneva: World Health Organization. hdl:10665/382243.
  6. ^ a b Page Module:Citation/CS1/styles.css has no content.British national formulary: BNF 76 (76 ed.). Pharmaceutical Press. 2018. pp. 625–626. ISBN 978-0-85711-338-2.
  7. ^ Page Module:Citation/CS1/styles.css has no content."Top 300 of 2023". ClinCalc. Archived from the original on 12 August 2025. Retrieved 12 August 2025.
  8. ^ a b Page Module:Citation/CS1/styles.css has no content."Valacyclovir Drug Usage Statistics, United States, 2014 - 2023". ClinCalc. Retrieved 18 August 2025.
  9. ^ a b Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006. Template:ISBN[page needed]
  10. ^ Page Module:Citation/CS1/styles.css has no content.Lille HM, Wassilew SW (2006). "Antiviral therapies of shingles in dermatology". In Gross G, Doerr H (eds.). Herpes zoroster: recent aspects of diagnosis and control. Monographs in virology. Vol. 26. Basel (Switzerland): Karger Publishers. p. 124. ISBN 978-3-8055-7982-7. Retrieved 1 January 2012.
  11. ^ Page Module:Citation/CS1/styles.css has no content.Elad S, Zadik Y, Hewson I, Hovan A, Correa ME, Logan R, et al. (August 2010). "A systematic review of viral infections associated with oral involvement in cancer patients: a spotlight on Herpesviridea". Support Care Cancer. 18 (8): 993–1006. doi:10.1007/s00520-010-0900-3. PMID 20544224. S2CID 2969472.
  12. ^ a b Page Module:Citation/CS1/styles.css has no content.Balfour HH, Hokanson KM, Schacherer RM (December 2005). A controlled trial of valacyclovir in infectious mononucleosis. 45th Interscience Conference on Antimicrobial Agents and Chemotherapy. Washington, DC. pp. 16–19. Abstract V1392.
  13. ^ a b Page Module:Citation/CS1/styles.css has no content.Simon MW, Deeter RG, Shahan B (March 2003). "The Effect of Valacyclovir and Prednisolone in Reducing Symptoms of EBV Illness In Children: A Double-Blind, Placebo-Controlled Study". International Pediatrics. 18 (3): 164–169 – via ResearchGate.
  14. ^ a b Page Module:Citation/CS1/styles.css has no content.Balfour HH, Hokanson KM, Schacherer RM, Fietzer CM, Schmeling DO, Holman CJ, et al. (May 2007). "A virologic pilot study of valacyclovir in infectious mononucleosis". Journal of Clinical Virology. 39 (1): 16–21. doi:10.1016/j.jcv.2007.02.002. PMID 17369082.
  15. ^ a b Page Module:Citation/CS1/styles.css has no content."Herpes B Virus: Information For Healthcare Providers". U.S. Centers for Disease Control and Prevention (CDC). 31 January 2019. Retrieved 22 May 2022.
  16. ^ Page Module:Citation/CS1/styles.css has no content.Baugh RF, Basura GJ, Ishii LE, Schwartz SR, Drumheller CM, Burkholder R, et al. (November 2013). "Clinical practice guideline: Bell's palsy". Otolaryngology–Head and Neck Surgery. 149 (3_suppl): S1–S27. doi:10.1177/0194599813505967. PMID 24189771. S2CID 36915347.
  17. ^ Page Module:Citation/CS1/styles.css has no content.Gagyor I, Madhok VB, Daly F, Sullivan F (September 2019). "Antiviral treatment for Bell's palsy (idiopathic facial paralysis)". Cochrane Database Syst Rev. 2019 (9) CD001869. doi:10.1002/14651858.CD001869.pub9. PMC 6726970. PMID 31486071.
  18. ^ Page Module:Citation/CS1/styles.css has no content."Valaciclovir (VCV) - USCN LIFE SCIENCE INC". www.uscnk.us.{{cite web}}: CS1 maint: deprecated archival service (link)
  19. ^ a b Page Module:Citation/CS1/styles.css has no content.O'Brien JJ, Campoli-Richards DM (March 1989). "Acyclovir. An updated review of its antiviral activity, pharmacokinetic properties and therapeutic efficacy". Drugs. 37 (3): 233–309. doi:10.2165/00003495-198937030-00002. PMID 2653790. S2CID 240858022.
  20. ^ Page Module:Citation/CS1/styles.css has no content.De Paor M, O'Brien K, Smith SM (2016). "Antiviral agents for infectious mononucleosis (glandular fever)". The Cochrane Database of Systematic Reviews. 2016 (12) CD011487. doi:10.1002/14651858.CD011487.pub2. PMC 6463965. PMID 27933614.
  21. ^ Page Module:Citation/CS1/styles.css has no content.Sweetman SC, ed. (2005). Martindale: the complete drug reference (34th ed.). London: Pharmaceutical Press. ISBN 0-85369-550-4. OCLC 56903116.[page needed]
  22. ^ Page Module:Citation/CS1/styles.css has no content.Cohen JI, Davenport DS, Stewart JA, Deitchman S, Hilliard JK, Chapman LE (November 2002). "Recommendations for prevention of and therapy for exposure to B virus (cercopithecine herpesvirus 1)". Clin Infect Dis. 35 (10): 1191–203. doi:10.1086/344754. PMID 12410479. S2CID 4652818.
  23. ^ Page Template:Citation/styles.css has no content.EP patent 308065, Krenitsky, Thomas Anthony & Beauchamp, Lilia Marie, "Therapeutic nucleosides", published Script error: No such module "auto date formatter"., assigned to Wellcome Foundation 
  24. ^ Page Module:Citation/CS1/styles.css has no content.Vardanyan R, Hruby V (2016). "34: Antiviral Drugs". Synthesis of Best-Seller Drugs. p. 709. doi:10.1016/B978-0-12-411492-0.00034-1. ISBN 978-0-12-411492-0. S2CID 75449475.
  25. ^ Page Module:Citation/CS1/styles.css has no content."The Top 300 of 2022". ClinCalc. Archived from the original on 30 August 2024. Retrieved 30 August 2024.
  26. ^ Page Module:Citation/CS1/styles.css has no content.Ahmed R (27 November 2009). "Ranbaxy Launches Generic Valtrex in U.S." The Wall Street Journal. Retrieved 16 January 2010.

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