Efinaconazole: first global approval.

Article Details

Citation

Patel T, Dhillon S

Efinaconazole: first global approval.

Drugs. 2013 Nov;73(17):1977-83. doi: 10.1007/s40265-013-0152-x.

PubMed ID
24249649 [ View in PubMed
]
Abstract

A non-lacquer 10% topical solution of efinaconazole, developed by Valeant Pharmaceuticals International, received its first global approval in Canada in October 2013 for the treatment of onychomycosis. The product is under regulatory review in the US and Japan. The mechanism of anti-fungal activity of efinaconazole, a small-molecule triazole compound, appears to be similar to that of other anti-fungal triazoles, namely ergosterol synthesis inhibition. In particular, it appears to inhibit 14alpha demethylase, an enzyme involved in the conversion of lanosterol to ergosterol, resulting in secondary degenerative changes. This article summarizes the milestones in the development of efinaconazole leading to this first approval for onychomycosis.

DrugBank Data that Cites this Article

Drugs
Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
EfinaconazoleLanosterol 14-alpha demethylaseProtein
Yes
Inhibitor
Details