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Keep this study
Lead
NanoBio Corporation
The purpose of the study is to determine whether NB002, 0.25%, and 0.5% are safe and effective in the treatment of distal subungual onychomycosis of the toenail.
Age
18–75
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
are healthy males or females between the ages of 18 and 75 years of age;
have a clinical diagnosis of mild to moderate DSO in the nail of at least one great toe, involving 25%-67% of the nail, without lunular or proximal involvement;
positive mycology results (ie, KOH test and culture of a dermatophyte) from the target great toenail;
refrain from using any lotions, creams, liquids, or polish on treated toenails or on the skin immediately adjacent to the toenails during the treatment period unless directed to do so by the investigator;
are willing to refrain from using topical steroids or topical antifungals on toenails or the skin immediately adjacent to the toenails; or systemic antifungals for the duration of the study;
You may not be if
females who are pregnant, plan to become pregnant during the study, or are nursing a child;
are hypersensitive to topical creams, ointments, medications, or surfactants;
have received systemic antifungal therapy for any reason within 3 months, or topical antifungal therapy on the toenails or skin immediately adjacent to the toenails within 3 weeks prior to the start of the study; or
have taken any investigational drug within 4 weeks prior to the start of the study.
Clareo Health | Treatment of Mild to Moderate Distal Subungual Onychomycosis of the Toenail
