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Safety and Efficacy Study of Subjects With Onychomycosis of the Great Toenail

Onychomycosis Clinical Trial

Official title:
An Open-Label, Rising Multiple-Dose, Multi-Center Study to Evaluate the Safety and Efficacy of Topically Applied AN2690 5.0% and 7.5% Solution for the Treatment of Adult Subjects With Onychomycosis of the Great Toenail

Clinical Trial Summary

The purpose of the study is to determine the safety and efficacy of 5.0% and 7.5% AN2690 Solution in the treatment of distal, subungual onychomycosis of the great target toenail.

Clinical Trial Description

The first group of 30 protocol-qualified subjects will be assigned to Treatment Group 1 and given 5% AN2690 Solution. Provided that there is adequate evidence of clinical safety after two weeks of dosing with 5% AN2690 Solution, a second group of 30 protocol-qualified subjects will be assigned to Treatment Group 2 and given 7.5% AN2690 Solution. A third group of 30 subjects will be enrolled and assigned the highest safe concentration of AN2690 evaluated in this study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00679523
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 2
Start date November 2005
Completion date February 2007
View Details
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