Lentiviral Gene Therapy for X-Linked Chronic Granulomatous Disease (X-CGD)
NCT ID: NCT01381003
Last Updated: 2012-06-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE1/PHASE2
INTERVENTIONAL
2011-11-30
2016-11-30
Brief Summary
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In many cases, patients can be protected from infection by constant intake of antibiotics. However, in others potential life-threatening infections break through. In some cases patients also develop serious inflammation requiring high doses of drugs such as steroids. CGD can be cured by bone marrow transplant, but the best results are available when there is matched donor available. Transplant from unmatched donor have a much worse outcome.
Gene therapy of CGD can be performed by introducing a normal copy of human gp91-phox gene into the blood forming stem cells of patients' bone marrow by using a gene carrier (in this study called lentiviral vector). After treatment of the bone marrow cells in a specialised laboratory are given back to the patient and will grow into functional phagocytic cells.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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pCCLchimGp91s lentiviral vector transduced CD34+ cells
pCCLchimGp91s lentiviral vector transduced CD34+ cells will be infused in a volume of 50-100 mls intravenously over 30-45 minutes
pCCLchimGp91s lentiviral vector transduced CD34+ cells infusion
pCCLchimGp91s lentiviral vector transduced CD34+ cells will be infused in a volume of 50-100 mls intravenously over 30-45 minutes
Interventions
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pCCLchimGp91s lentiviral vector transduced CD34+ cells infusion
pCCLchimGp91s lentiviral vector transduced CD34+ cells will be infused in a volume of 50-100 mls intravenously over 30-45 minutes
Eligibility Criteria
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Inclusion Criteria
* Molecular diagnosis confirmed by DNA sequencing and supported by laboratory evidence for absent or significantly reduced biochemical activities of the NADPH-oxidase
* Parental/Guardian and where appropriate Child's signed consent/assent
Exclusion Criteria
* Contraindication for leukapheresis (anaemia Hb \<8g/dl, cardiovascular instability, severe coagulopathy) or for administration of conditioning medication
30 Years
MALE
No
Sponsors
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Great Ormond Street Hospital for Children NHS Foundation Trust
OTHER
Responsible Party
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Great Ormond Street Hospital for Children NHS Trust
Principal Investigators
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Adrian Thrasher, Professor
Role: PRINCIPAL_INVESTIGATOR
Great Ormond Street Hospital for Children NHS Foundation Trust
Locations
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Great Ormond Street Hospital for Children NHS Trust
London, London, United Kingdom
Countries
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Other Identifiers
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11-MI-03
Identifier Type: -
Identifier Source: org_study_id
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