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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT00108134
Registration number
NCT00108134
Ethics application status
Date submitted
14/04/2005
Date registered
15/04/2005
Date last updated
24/12/2008
Titles & IDs
Public title
Study to Determine the Safety of Two Applications of PEP005 Topical Gel to Superficial Basal Cell Carcinoma
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Scientific title
A Multi-Center, Randomized, Double-Blind, Parallel-Group, Vehicle-Controlled Study to Determine the Safety of PEP005 0.0025%, 0.01% and 0.05% Gel With Two Treatment Schedules, Day 1 & 2 or Day 1 & 8 Applications to Superficial Basal Cell Carcinoma
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Secondary ID [1]
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2005/154
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Secondary ID [2]
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PEP005-003
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Basal Cell Carcinoma
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Condition category
Condition code
Cancer
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Non melanoma skin cancer
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Cancer
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Kidney
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - PEP005
Treatment: Drugs: PEP005
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Safety
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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Efficacy
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Assessment method [1]
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Timepoint [1]
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Eligibility
Key inclusion criteria
- Male or female patients at least 18 years of age
- One sBCC on the arm, shoulder, chest, face, neck, abdomen, leg, back or scalp suitable
for surgical excision
- Histological confirmation of sBCC based on the central dermatopathologist's evaluation
of the punch biopsy
- Longest pre- and post-biopsy diameter of the sBCC lesion between 4 mm and 15 mm
- Maximum thickness of 4 mm of the sBCC lesion
- Laboratory values within the reference ranges as defined by the central laboratory or
"out of range" test results that are clinically acceptable to the Investigator
- Ability to follow study instructions and likely to complete all study requirements
- Written informed consent
- Male patients with a female partner of childbearing potential must use an approved
form of contraception during the study and for 4 weeks after the last visit
- Agreement from the patient to allow photographs of all selected lesions (including the
face) to be taken and used as part of the study data package
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Location of the outside margin of the anticipated treatment area of the sBCC selected
for treatment:
1. within 10 cm of a malignant lesion that will require treatment during the study
2. within 5 cm of an incompletely healed wound
3. within 2 cm of a pre-malignant lesion (e.g. actinic keratosis lesion)
4. within 2 cm of the open eyelid margins
5. within 1 cm of a scar or an area previously treated with surgical excision
6. on the lips
7. on the breast
8. on the hand or foot
9. in a skin crease
- sBCC lesion selected for treatment requiring Mohs micrographic surgery
- Presence of known or suspected metastatic disease
- Histological evidence of actinic keratoses or nBCC in the screening visit biopsy
sample
- Histological evidence of BCC with micro-nodular features or squamous metaplasia,
sclerosing BCC (i.e. desmoplastic or morphoeic), or BCC with perineural involvement in
the screening visit biopsy sample
- History of recurrence of the sBCC lesion
- History or evidence of skin diseases which would interfere with evaluation of the
treatment area (e.g. eczema, unstable psoriasis, xeroderma pigmentosa)
- Known sensitivity to any of the ingredients in the study medication
- A cosmetic or therapeutic procedure (e.g. use of liquid nitrogen, surgical excision,
curettage, dermabrasion, medium or greater depth chemical peel, laser resurfacing)
within 10 cm of the selected sBCC lesion during the 3 months prior to study entry or
anticipated treatment within 10 cm of the selected lesion during the study
- Treatment with 5-fluorouracil, imiquimod, diclofenac or photodynamic therapy:
1. of lesions located within 10 cm of the selected sBCC lesion during the 3 months
prior to study entry or
2. anywhere during the 4 weeks prior to study entry or anticipated treatment during
the study
- Use of acid-containing products (e.g. salicylic acids or fruit acids, such as alpha
and beta hydroxy acids and glycolic acids), topical retinoids or light chemical peels
within 10 cm of the selected sBCC lesion during the 3 months prior to study entry or
anticipated treatment in this same area during the study
- Treatment with immuno-modulators (e.g. cyclosporine, prednisone, methotrexate,
infliximab or other biological agents), cytotoxic drugs (e.g. vinblastine,
cyclophosphamide, azathioprine, chlorambucil, methotrexate), or interferon/interferon
inducers during the 4 weeks prior to study entry or anticipated treatment during the
study
- Treatment with psoralen plus UVA or use of UVB therapy during the 6 months prior to
study entry or anticipated treatment during the study
- Use of systemic retinoids (e.g. isotretinoin, acitretin) during the 6 months prior to
study entry or anticipated treatment during the study
- Anticipated excessive or prolonged exposure to ultraviolet light (e.g. sunlight,
tanning beds) or use of topical salves, creams or ointments to the selected lesion
during the study
- Anticipated need for hospitalization or non-dermatological surgery during the study
- Concurrent disease that suppresses the immune system (e.g. HIV) or uncontrolled
systemic disease (e.g. uncontrolled hypertension, poorly controlled diabetes)
- Current evidence of chronic alcohol or drug abuse
- Current enrolment in an investigational drug or device study or participation in such
a study within 30 days of entry into this study
- Diagnosis of xeroderma pigmentosa or Gorlin Syndrome (i.e. Basal Cell Nevus Syndrome)
- A condition or situation which in the Investigator's opinion may put the patient at
significant risk, may confound the study results, or may interfere significantly with
the patient's participation in the study
- Females of child bearing potential (a female is considered of childbearing potential
unless she is postmenopausal, i.e., no menses for at least 12 consecutive months, or
is without a uterus)
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/03/2005
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/03/2006
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC,WA
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Recruitment hospital [1]
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Southderm Pty Ltd - Sydney
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Recruitment hospital [2]
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St George Dermatology & Skin Cancer Centre - Sydney
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Recruitment hospital [3]
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Siller Medical - Brisbane
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Recruitment hospital [4]
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Belmont Specialist Centre - Brisbane
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Recruitment hospital [5]
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The Skin Centre - Gold Coast
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Recruitment hospital [6]
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Skin and Cancer Foundation - Melbourne
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Recruitment hospital [7]
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Freemantle Dermatology - Freemantle
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Recruitment hospital [8]
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Private Dermaology Clinic - Fremantle
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Recruitment hospital [9]
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St John of God Dermatology - Subiaco
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Recruitment postcode(s) [1]
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2010 - Sydney
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Recruitment postcode(s) [2]
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2217 - Sydney
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Recruitment postcode(s) [3]
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4000 - Brisbane
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Recruitment postcode(s) [4]
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4152 - Brisbane
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Recruitment postcode(s) [5]
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4217 - Gold Coast
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Recruitment postcode(s) [6]
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3053 - Melbourne
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Recruitment postcode(s) [7]
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6160 - Freemantle
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Recruitment postcode(s) [8]
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6160 - Fremantle
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Recruitment postcode(s) [9]
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6008 - Subiaco
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Peplin
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this study is to determine whether topical application of PEP005 is safe for
the treatment of superficial basal cell carcinoma.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT00108134
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Greg Siller
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT00108134
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