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Trial registered on ANZCTR
Registration number
ACTRN12605000213640
Ethics application status
Approved
Date submitted
23/08/2005
Date registered
25/08/2005
Date last updated
19/01/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Infusion of donor-derived CMV peptide-specific CTL after allogeneic HSCT
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Scientific title
A Phase I clinical trial of infusion of donor-derived HLA-A*0201-restricted CMV pp65 peptide-specific CTL to reconstitute CMV-specific immunity after allogeneic haematopoietic stem cell transplantation.
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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:
Immune reconstitution post-allogeneic haematopoietic stem cell transplantation
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Condition category
Condition code
Other
333
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0
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Other blood disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Phase I study of intravenous infusion of monocyte-derived dendritic cell-primed, donor-derived, HLA-A*0201-restricted, CMV pp65 peptide-specific in vitro expanded cytotoxic T lymphocytes on or after day 28 post stem cell infusion.
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Intervention code [1]
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Prevention
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Comparator / control treatment
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Safety of donor-derived CMV-specific CTL infusion post-transplant
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Assessment method [1]
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Timepoint [1]
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Primary outcome [2]
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Feasibility of donor-derived CMV-specific CTL infusion post-transplant
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Assessment method [2]
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Timepoint [2]
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Secondary outcome [1]
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Persistence/reconstitution of CMV-specific CTL.
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Assessment method [1]
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Timepoint [1]
859
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Eligibility
Key inclusion criteria
HLA-A*0201 pos and CMV seropositive donor, 5/6 or 6/6 sib match or 6/6/MUD, GVHD < grade II at the time of infusion, >day 28 post allogeneic HSCT, no recent anti-lymphocyte globulin.
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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
No exclusion criteria
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Study design
Purpose of the study
Prevention
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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
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/08/2001
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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
12
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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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Charities/Societies/Foundations
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Name [1]
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Leukaemia Foundation Clinical Research Fellowship
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Address [1]
393
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Country [1]
393
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Primary sponsor type
Hospital
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Name
Department of Haematology, Westmead Hospital
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Address
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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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Nil
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Address [1]
322
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Country [1]
322
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Westmead Hospital
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
1382
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Approval date [1]
1382
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Ethics approval number [1]
1382
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Ethics committee name [2]
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Children's Hospital, Westmead
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Ethics committee address [2]
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
1383
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Approval date [2]
1383
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Ethics approval number [2]
1383
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Summary
Brief summary
CMV infection or reactivation causes morbidity and mortality in patients after allogeneic HSCT. We aim to adoptively transfer donor-derived CMV-specific CTL to prevent CMV infection and reactivation in these patients.
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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
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Email
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Contact person for public queries
Name
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A/Prof David Gottlieb
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Address
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Department of Haematology
Westmead Hospital
Westmead NSW 2145
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Country
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Australia
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Phone
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+61 2 98456352
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Ken Mickelthwaite
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Address
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Leukaemia Research Laboratory
Westmead Millennium Institute
Westmead NSW 2145
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Country
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Australia
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Phone
348
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+61 2 98456352
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Fax
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Email
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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
Source
Title
Year of Publication
DOI
Dimensions AI
Cytomegalovirus-Specific Cytotoxic T Lymphocytes Can Be Efficiently Expanded from Granulocyte Colony-Stimulating Factor–Mobilized Hemopoietic Progenitor Cell Products Ex Vivo and Safely Transferred to Stem Cell Transplantation Recipients to Facilitate Immune Reconstitution
2013
https://doi.org/10.1016/j.bbmt.2013.01.021
N.B. These documents automatically identified may not have been verified by the study sponsor.
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