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Topical n-docosanol for management of recurrent herpes labialis.

AbstractIMPORTANCE OF THE FIELD:
Recurrent herpes labialis (RHL) is a significant disorder with social and health consequences that affects upwards of 20 - 40% of the adult population. Docosanol is the only FDA-approved topical agent that is available over the counter for management of RHL. Its mechanism of action is unique compared with other available antiviral agents.
AREAS COVERED IN THIS REVIEW:
The authors conducted a comprehensive search of the published preclinical and clinical literature on topical docosanol for RHL. All of the published literature relating to docosanol and its use for the management of recurrent herpes labialis was reviewed, from the first report of docosanol to 31 January 2010.
WHAT THE READER WILL GAIN:
The objective of this review was to summarize and critically evaluate the available literature with respect to topical docosanol's mechanism, safety and efficacy in the management of RHL.
TAKE HOME MESSAGE:
Ten percent docosanol cream is a safe and effective topical treatment for the management of RHL in immunocompetent adults, with essentially equivalent efficacy compared with other available prescription topical antiviral agents. Owing to its unique mechanism of action, there is little to no risk of developing resistance.
AuthorsNathaniel S Treister, Sook-Bin Woo
JournalExpert opinion on pharmacotherapy (Expert Opin Pharmacother) Vol. 11 Issue 5 Pg. 853-60 (Apr 2010) ISSN: 1744-7666 [Electronic] England
PMID20210688 (Publication Type: Journal Article, Review)
Chemical References
  • Antiviral Agents
  • Fatty Alcohols
  • Nonprescription Drugs
  • docosanol
Topics
  • Administration, Topical
  • Adult
  • Animals
  • Antiviral Agents (administration & dosage, pharmacology, therapeutic use)
  • Drug Approval
  • Fatty Alcohols (administration & dosage, pharmacology, therapeutic use)
  • Herpes Labialis (drug therapy, virology)
  • Humans
  • Nonprescription Drugs
  • Recurrence
  • United States
  • United States Food and Drug Administration

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