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Pharmacokinetics, Safety, and Tolerability of Oxfendazole in Healthy Volunteers: a Randomized, Placebo-Controlled First-in-Human Single-Dose Escalation Study
Author(s) -
Guohua An,
Daryl J. Murry,
Kiran Gajurel,
Thanh Bach,
Greg A. Deye,
Larissa V. Stebounova,
Ellen E. Codd,
John Horton,
Armando E. González,
Héctor H. Garcı́a,
Dilek İnce,
Denice HodgsonZingman,
Effie Nomicos,
Thomas Conrad,
Jessie K. Kennedy,
W. Jones,
Robert H. Gilman,
Patricia Winokur
Publication year - 2019
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02255-18
Subject(s) - oxfendazole , neurocysticercosis , anthelmintic , cysticercosis , tolerability , taenia solium , medicine , pharmacokinetics , pharmacology , placebo , taeniasis , adverse effect , cestode infections , veterinary medicine , immunology , pathology , helminths , fenbendazole , alternative medicine
Cysticercosis is a parasitic disease that frequently involves the human central nervous system (CNS), and current treatment options are limited. Oxfendazole, a veterinary medicine belonging to the benzimidazole family of anthelmintic drugs, has demonstrated substantial activity against the tissue stages ofTaenia solium and has potential to be developed as an effective therapy for neurocysticercosis.

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