drugset / Trial / NCT01841996

Pharmacokinetics and Safety Study of ME1111 in Moderate to Severe Onychomycosis Patients

NCT01841996 ↗

Phase 1 Completed 24 enrolled Meiji Seika Pharma Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is Randomized, Double-Blind, Vehicle-Controlled, Multiple-Dose Study. The purpose is to determine the safety, tolerability, systemic exposure and pharmacokinetics of ME1111 after repeated daily topical application of ME1111 in a maximal use setting in adults with distal subungual onychomycosis of the toenails.

Timeline

Start
2013-03
Primary completion
2013-08
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject ME1111 Unknown — Topical

Indications