Terbinafine and
itraconazole are the most commonly used oral antifungals to treat
onychomycosis and superficial
dermatomycoses. Recently, poor response to oral
terbinafine has been reported. We have summarized the most appropriate dosing regimens of
posaconazole, fosravuconazole,
voriconazole, and oteseconazole (VT-1161) to treat
onychomycosis and superficial
fungal infections. A structured search on PubMed and Google Scholar was conducted. Additionally, the bibliographies of selected articles were searched to identify relevant records. The number of records identified from the searches was 463, with 50 articles meeting the inclusion criteria for review. None of the new
azoles are US FDA approved for
onychomycosis treatment; however, an increasing number of studies have evaluated these agents. The efficacies (complete cure and mycologic cure) of the
antifungal agents for dermatophyte great toenail
onychomycosis treatment are
terbinafine 250 mg/day × 12 weeks (Phase III trial) (38%, 70%),
itraconazole 200 mg/day × 12 weeks (Phase III trial) (14%, 54%),
posaconazole 200 mg/day × 24 weeks (Phase IIB) (54.1%, 70.3%), fosravuconazole 100 mg/day
ravuconazole equivalent × 12 weeks (Phase III) (59.4%, 82.0%), and oteseconazole 300 mg/day loading dose × 2 weeks (Phase II), followed by 300 mg/week × 10 weeks (maintenance dose) (45%, 70%). Guidelines for monitoring are also presented.