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BPX-501 T Cells Infused Post Stem Cell Transplant in Pediatrics With Non-Malignant Disorders Ineligible for BPU004 Study
Not Recruiting
Trial ID: NCT03639844
Purpose
Providing access of BPX-501 gene modified T cells and rimiducid to pediatric patients who do not meet the eligibility criteria of the BP-U-004 study.
Official Title
Expanded Access Protocol for CaspaCIDe T Cells From An HLA-Partially Matched Related Donor After Negative Selection of TCR αβ+T Cells In Pediatric Patients Affected by Hematological and Other Disorders
Stanford Investigator(s)
Rajni Agarwal-Hashmi
Professor of Pediatrics (Stem Cell Transplantation)
Eligibility
Inclusion Criteria:
1. Males or females
2. Age \< 21 years and \> 3 months
3. Life expectancy \> 10 weeks
4. Patients deemed eligible for allogeneic stem cell transplantation.
5. Non-malignant disorders including:
1. inherited metabolic disorders such as adrenal leukodystrophy;
2. lysosomal storage disorders such as Hurler syndrome or metachromatic leukodystrophy
3. other inborn errors of metabolism
6. Lack of suitable conventional donor (HLA identical sibling or HLA phenotypically identical relative evaluated using high resolution molecular typing).
7. A minimum genotypic identical match of 5/10 is required.
8. The donor and recipient must be identical, as determined by high resolution typing, at least one allele of each of the following genetic loci: HLA-A, HLA-B, HLA-Cw, and HLA- DRB1.
9. Lansky/Karnofsky score \> 50
10. Signed written informed consent
3.2 Subject exclusion criteria
1. Age \< 3 months or \>21 years
2. Patients with non-malignant disorders eligible for treatment on the BP-U-004 study:
1. primary immune deficiencies,
2. severe aplastic anemia not responding to immune suppressive therapy,
3. osteopetrosis,
4. selected cases of hemoglobinopathies and
5. congenital/hereditary cytopenia, including Fanconi Anemia before any clonal malignant evolution (MDS, AML)
3. Greater than Grade II acute GVHD or chronic extensive GVHD due to a previous allograft at the time of inclusion
4. Patient receiving an immunosuppressive treatment for GVHD treatment due to a previous allograft at the time of inclusion
5. Dysfunction of liver (ALT/AST \> 5 times normal value, or bilirubin \> 3 times normal value), or of renal function (creatinine clearance \< 30 ml / min)
6. Severe cardiovascular disease (arrhythmias requiring chronic treatment, congestive heart failure or left ventricular ejection fraction \< 40%)
7. Current active infectious disease (including positive HIV serology or viral RNA)
8. Serious concurrent uncontrolled medical disorder
9. Pregnant or breast feeding female patient
10. Lack of parents'/guardian's informed consent.
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Intervention(s):
biological: rivogenlecleucel
drug: rimiducid
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305