The purpose of this study is to determine whether topical application of PEP005 is safe for the treatment of actinic keratoses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
60
Royal Prince Alfred Hospital
Sydney, New South Wales, Australia
Siller Medical
Brisbane, Queensland, Australia
Skin and Cancer Foundation
Melbourne, Victoria, Australia
Monash Medical Centre
Melbourne, Victoria, Australia
To determine the safety of PEP005 Topical Gel at 0.0025%, 0.01%, and 0.05% administered as two applications to patients with actinic keratosis (AKs) on the arms, shoulders, chest, face, and/or scalp
Time frame: 85 days
To evaluate the efficacy of PEP005 0.0025%, 0.01% and 0.05% Topical Gel in treating Actinic Keratoses
Time frame: 85 days
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Vehicle Gel (Day 1,2 application)
0.0025% PEP005 Topical Gel (Day 1,8 application)
0.01% PEP005 Topical Gel (Day 1,8 application)
0.05% PEP005 Topical Gel (Day 1,8 application)
Vehicle Gel (Day 1,8 application)
Fremantle Dermatology
Fremantle, Western Australia, Australia
Private Dermaology Clinic
Fremantle, Western Australia, Australia