The Sponsor has evaluated PK for the entire proposed duration of dosing (two weeks for
tinea pedis and one week for tinea cruris and tinea corporis). The mean ± SD values of AUC(0-t)
and Cmax on Day 15 for the parent drug were 18.74 ± 27.05 ng*h/mL and 0.93 ± 1.23 ng/mL
respectively, in subjects with tinea pedis, and 106.93 ± 57.57 ng*h/mL and 5.63 ± 2.31 ng/mL
respectively, on Day 8 in subjects with tinea cruris.