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Safety and Efficacy Evaluation of Topically Applied AN2690 Solutions for Subjects With Onychomycosis

Onychomycosis Clinical Trial

Official title:
An Open Label, Multi-center Study To Evaluate The Safety And Efficacy Of Topically Applied An2690 1% And 5% Solutions 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 1% and 5% AN2690 solutions in the treatment of distal, subungual onychomycosis of the great toenail.

Clinical Trial Description

The first group of 30 protocol-qualified subjects will be assigned to Treatment Group 1 and given 1% AN2690 Solution. The second group of 30 protocol-qualified subjects will be assigned to Treatment Group 2 and given 5% AN2690 Solution. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00680134
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 2
Start date June 30, 2006
Completion date August 31, 2007
View Details
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