The purpose of this study is to evaluate the safety and efficacy of topical application of IDP-108 versus vehicle in treating patients with onychomycosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
780
Percentage of patients who achieve clinical cure
Time frame: 52 weeks
Percentage of patients who achieve clinical efficacy
Time frame: 52 weeks
Percentage of patients who achieve mycologic cure
Time frame: 52 weeks
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