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Efficacy and Safety of NAFT-600 in Subjects With Tinea Pedis — NAFT-600  

Tinea Pedis Clinical Trial

Official title:
A Phase 3 Double-Blind, Randomized, Placebo-Controlled,Multicenter, Parallel Group Evaluation of the Efficacy and Safety of NAFT-600 in Subjects With Tinea Pedis

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of NAFT-600, applied once daily for 2 weeks, when compared to placebo for 2 weeks in the treatment of subjects with tinea pedis.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01289015
Study type Interventional
Source Merz Pharmaceuticals, LLC
Contact
Status Completed
Phase Phase 3
Start date February 2011
Completion date January 2012
View Details
See also
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