Safety and Efficacy of Luliconazole Solution, 10% in Subjects With Mild to Moderate Onychomycosis — SOLUTION  

Distal and Lateral Subungual Onychomycosis Clinical Trial

Official title: Safety and Efficacy of Luliconazole Solution, 10% With Two Dosing Regimens in Distal Subungual Onychomycosis of the Toenails: A Randomized, Double-Blind, Vehicle-Controlled, Phase 2B/3 Study

Status Completed

Clinical Trial Summary

The purpose of this study is to determine the safety and efficacy of a topical antifungal formulation, Luliconazole Solution, 10%, in the treatment of adults with onychomycosis of the toenails.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

• Distal and Lateral Subungual Onychomycosis
• Onychomycosis

• NCT number: NCT01431820
• Study type: Interventional
• Source: Topica Pharmaceuticals
• Status: Completed
• Phase: Phase 2/Phase 3
• Start date: May 2012
• Completion date: August 2014