Status and phase
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About
The purpose of this trial is to compare the rate of complete clearance of actinic keratosis (AK) using sequential cryotherapy and field treatment with PEP005 Gel compared to cryotherapy alone.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Subjects must be competent to understand the nature of the trial and provide informed consent.
Subjects with 4 to 8 clinically typical, visible and discrete AKs within a contiguous 25 cm2 treatment area on the face or scalp.
Subject at least 18 years of age.
Female subjects must be of either:
Female subjects of childbearing potential must be willing to use effective contraception.
Exclusion criteria
Location of the selected treatment area:
Prior treatment with PEP005 Gel on face or scalp.
Selected treatment area lesions that have:
History or evidence of skin conditions other than the trial indication that would interfere with evaluation of the trial medication
Clinical diagnosis/history or evidence of any medical condition that would expose a subject to an undue risk of a significant AE or interfere with assessments of safety and efficacy.
Any abnormal vital signs measurements that are medically significant or would impact the safety of the subject or the interpretation of the trial results.
Anticipated need for hospitalization or out-patient surgery during the first 15 days after the first trial medication application.
Known sensitivity or allergy to any of the ingredients in PEP005 Gel
Recent excessive exposure to ultraviolet light
Current enrolment or participation in a clinical trial within 30 days of entry into this study
Subjects previously randomised in the trial
Female subjects who are breastfeeding
Prohibited Therapies and/or Medications within 2 weeks prior to Visit 1
Prohibited Therapies and/or Medications: within 4 weeks prior to visit 1:
Prohibited Therapies and/or Medications within 8 weeks prior to visit 1:
Prohibited Therapies and/or Medications within 6 months prior to visit 1
Primary purpose
Allocation
Interventional model
Masking
367 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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