drugset / Trial / NCT02483182

Safety, Tolerability and Therapeutic Efficacy of Topical ZEP-3 Ointment (1.0%) for the Treatment of Cold Sores

NCT02483182

Phase 2 Completed 210 enrolled Shulov Innovate for Science Ltd. 2012
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a phase II, prospective, randomized, double-blind, parallel group, acyclovir-controlled clinical study to evaluate the safety, tolerability and preliminary therapeutic efficacy of ZEP-3 ointment 1.0% for the treatment of cold sores (Herpes labialis), following five consecutive treatment days with five times daily topical administration.

Timeline

Start
2015-09
Primary completion
2018-06-24
Completion
2018-06-24

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acyclovir Small molecule 5 % Topical
Subject ZEP-3 Peptide 1 % Topical

Indications