Cumulative Irritation Test

Status Completed

Clinical Trial Summary

The purpose of this study is to determine the cumulative irritation potential of the products listed by the Sponsor.

Clinical Trial Description

Healthy, adult volunteers of either sex will be patched on his/her back with AN2690 Solution 2.5%, AN2690 Solution 5%, AN2690 Solution 7.5%, AN2690 Solution Vehicle and Sodium Laurel Sulfate 0.5% over the course of 21 consecutive days. After 24 hours, the patches are to be removed and the site evaluated using a five-point scale for irritation. ;

Study Design

Related Conditions & MeSH terms

Onychomycosis

Clinical Trial Details

NCT number	NCT00680095
Study type	Interventional
Source	Pfizer
Contact
Status	Completed
Phase	Phase 1
Start date	January 22, 2007
Completion date	February 19, 2007

View Details

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