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The purpose of this study is to determine the cumulative irritation potential of the products listed by the Sponsor.
Condition |
Intervention |
Phase |
Onychomycosis |
Drug: AN2690
Other: AN2690 Solution, Vehicle
Other: Sodium Lauryl Sulfate, 0.5% |
Phase 1 |
Study Type: |
Interventional |
Study Design: |
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label |
Official Title: |
21-Day Cumulative Irritation Test |
Date of article/Start date of trial: 8 May 2008
Trial Phase: Phase 1
clinical Trials Gov ID: NCT00680095
Trial status: Completed