Efficacy, Safety, and Tolerability of HTS-519 Insert in Patients With Toenail Fungus of the Big T… (NCT02798380) | Clinical Trial Compass
CompletedPhase 2
Efficacy, Safety, and Tolerability of HTS-519 Insert in Patients With Toenail Fungus of the Big Toenail
United States30 participantsStarted 2016-07
Plain-language summary
The purpose of this study is to assess the efficacy, safety and tolerability of HTS-519 Inserts in the treatment of mild to moderate toenail fungus disease of the big toenail.
Who can participate
Age range18 Years – 74 Years
SexALL
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Inclusion Criteria:
* Male and females 18 - 74 years of age inclusive
* Fungal toenail infection of one or both of the large (great) toenails
* The nail infection must be due to a dermatophyte, (mixed infections \[dermatophyte and non-dermatophyte\] are not allowed)
* Willingness not to have professional pedicures or application of any nail polish product or nail cosmetics to the toenails after the screening visit
Exclusion Criteria:
* History of any significant chronic fungal disease other than onychomycosis or immunocompromised condition
* Any abnormalities of the nail or previous surgery of the toenail that could prevent a normal appearing nail if clearing of infection is achieved
* Significant confounding conditions as assessed by the study doctor
* Participation in any other trial of an investigational drug or device within 30 days or participation in a research study concurrent with this study
* No administration of systemic antifungal medications within 6 months prior to screening visit
* No application of prescription topical antifungal medications for toenail fungus within 3 months or other commercially available topical medications for toenail fungus applied directly to the toenails within 1 month prior to screening visit
* Tinea pedis (athlete's foot) that would require systemic treatment
Other protocol-defined inclusion/exclusion criteria may apply