drugset / Trial / NCT02483182
Safety, Tolerability and Therapeutic Efficacy of Topical ZEP-3 Ointment (1.0%) for the Treatment of Cold Sores
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Acyclovir | Small molecule | 5 % | Topical |
| Subject | ZEP-3 | Peptide | 1 % | Topical |