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Oxfendazole: a promising agent for the treatment and control of helminth infections in humans.

AbstractINTRODUCTION:
Oxfendazole (methyl [5-(phenylsulphinyl)-1H benzimidazole-2-yl] carbamate) has a particularly long metabolic half-life in ruminants, and its metabolite fenbendazole also has anthelminthic action. A very limited number of drugs are available for the treatment of some zoonotic helminth infections, such as neurocysticercosis and echinococcosis. More recent work has expanded oxfendazole's nonclinical safety profile and demonstrated its safety and bioavailability in healthy human volunteers, thus advancing the possibility of a new and greatly needed option for antiparasitic treatment of geohelminths and tissue parasites. Areas covered: The present article reviews evidence supporting the safety and efficacy of oxfendazole against both gut and tissue dwelling helminths in animals, as well as more recent safety and pharmacokinetic data supporting its potential for use in human parasitoses. Expert commentary: The pharmacokinetics, safety, and wide spectrum of efficacy of oxfendazole are consistently demonstrated in intestinal helminth infections of animals as well as in tissue dwelling larval cestode and trematode infections in diverse animal species. Now supported by first-in-human safety and pharmacokinetic data, oxfendazole becomes a promising alternative to the limited portfolio of antiparasitic drugs available to treat helminthic diseases of humans.
AuthorsArmando E Gonzalez, Ellen E Codd, John Horton, Hector H Garcia, Robert H Gilman
JournalExpert review of anti-infective therapy (Expert Rev Anti Infect Ther) Vol. 17 Issue 1 Pg. 51-56 (01 2019) ISSN: 1744-8336 [Electronic] England
PMID30501436 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
Chemical References
  • Anthelmintics
  • Benzimidazoles
  • oxfendazole
Topics
  • Animals
  • Anthelmintics (adverse effects, pharmacokinetics, therapeutic use)
  • Benzimidazoles (adverse effects, pharmacokinetics, therapeutic use)
  • Biological Availability
  • Half-Life
  • Helminthiasis (drug therapy, parasitology)
  • Helminthiasis, Animal (drug therapy, parasitology)
  • Humans
  • Zoonoses (drug therapy, parasitology)

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