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 daily on his/her back with multiple strengths of AN2718 in 2 different topical dosage forms and an active comparator over the course of 21 consecutive days. Twenty-four hours after each application, the patches will be removed and the site evaluated using a five-point scale for irritation. ;

Study Design

Related Conditions & MeSH terms

Tinea Pedis

Clinical Trial Details

NCT number	NCT00781664
Study type	Interventional
Source	Pfizer
Contact
Status	Completed
Phase	Phase 1
Start date	October 2008
Completion date	November 2008

View Details

See also
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