drugset / Trial / NCT01223222

A Study to Evaluate Safety, Tolerability and Efficacy of Lytixar™ (LTX-109) on Uncomplicated, Gram-positive, Skin Infection

NCT01223222 ↗

Phase 2 Completed 24 enrolled Lytix Biopharma AS
RandomizedSingle-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of Lytixar™ applied topically to uncomplicated skin infections. Three dose levels of Lytixar™ (1%, 2% and 5%) versus placebo will be tested.

Timeline

Start
2010-09
Primary completion
2011-02
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator LTX-109 Peptide 1 % Topical
Comparator LTX-109 Peptide 2 % Topical
Comparator LTX-109 Peptide 5 % Topical