Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00546611

The Purpose of This Study is to Determine Whether Topical Application of PEP005 is Safe for the Treatment of Common Wart(s)

A Phase I, Single-Centre, Open-Label, Fixed-Dose Study of the Safety and Efficacy of up- to Three-Days Application of 0.05% PEP005 Topical Gel in the Treatment of Patients With Common Wart(s) (Verruca[e] Vulgaris) on the Dorsal Hand

Status
Withdrawn
Phase
Phase 1
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Peplin · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Verruca vulgaris, otherwise known as the common wart, is caused by the human papillomavirus (HPV). Common warts are generally located on the hands and feet, but can also occur elsewhere (e.g., any areas of frequent contact). Common warts have a characteristic cauliflower-like surface, are typically slightly raised above the surrounding skin and are generally diagnosed by visual inspection.The treatment of warts poses a therapeutic challenge for physicians. No single therapy has been proven effective at achieving complete remission in every patient.This study will aim to evaluate an up-to a three-day course of therapy with 0.05% PEP005 Topical Gel.

Conditions

Interventions

TypeNameDescription
DRUGPEP005

Timeline

Start date
2007-10-01
First posted
2007-10-19
Last updated
2016-01-28

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT00546611. Inclusion in this directory is not an endorsement.