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Trial registered on ANZCTR
Registration number
ACTRN12605000636651
Ethics application status
Approved
Date submitted
10/10/2005
Date registered
13/10/2005
Date last updated
13/12/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
Phase 1 Study of Coxsackievirus A21 for the treatment of melanoma
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Scientific title
Intratumoural administration of coxsackievirus A21 for the control of malignant melanoma.
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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:
Malignant Melanoma
764
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Condition category
Condition code
Cancer
840
840
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0
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Malignant melanoma
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A single intratumoural injection of coxsackievirus A21.
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Intervention code [1]
708
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Treatment: Drugs
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Comparator / control treatment
uncontrolled
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
1078
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Safety profile of treatment
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Assessment method [1]
1078
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Timepoint [1]
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Assessed three times weekly for 2 weeks, then weekly for 2 weeks.
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Primary outcome [2]
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Characterisation of adverse events
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Assessment method [2]
1079
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Timepoint [2]
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Assessed three times weekly for 2 weeks, then weekly for 2 weeks.
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Secondary outcome [1]
1998
0
Clinical response of injected and non-injected tumours.
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Assessment method [1]
1998
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Timepoint [1]
1998
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Assessed weekly for 4 weeks.
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Eligibility
Key inclusion criteria
Stage IV melanoma (AJCC)- minimum of 2 SC metastases- failure or refusal of standard chemotherapy- ECOG score of 0 or 1- other.
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Minimum age
Not stated
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Maximum age
Not stated
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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
Metastatic CNS disease- occular or mucosal melanoma- immunodeficiency- splenectomy- other.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised 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
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 1
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/09/2005
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Actual
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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
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Sample size
Target
3
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Viralytics Ltd.
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Address [1]
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8/33 Ryde Rd., Pymble, NSW 2073
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Country [1]
928
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Viralytics Ltd.
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Address
8/33 Ryde Rd., Pymble, NSW 2073
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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N/A
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Address [1]
787
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Country [1]
787
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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Trial website
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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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Address
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Country
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Phone
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Fax
35315
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Email
35315
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Contact person for public queries
Name
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Dr. Phillip Altman
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Address
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Melanoma Unit
Mater Misericordiae Hospital
Newcastle NSW 2298
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Country
9897
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Australia
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Phone
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+61 2 49850100
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Fax
9897
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Email
9897
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[email protected]
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Contact person for scientific queries
Name
825
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Phillip Altman
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Address
825
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8/33 Ryde Rd., Pymble, NSW 2073
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Country
825
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Australia
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Phone
825
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+61(2)94993200
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Fax
825
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+61(2)94993300
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Email
825
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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