Children's Hospital of Philadelphia
Timothy Olson
The goal of this protocol is to expand access for patients who lack a fully HLA (Human leukocyte antigen) matched sibling donor and who are candidates for allogeneic hematopoietic stem cell transplant (HSCT). These patients have a serious or immediately life-threatening disease for which HSCT is indicated. These patients are not eligible for other Children's Hospital of Philadelphia IRB approved protocols that utilize CliniMACs technology for T depletion.
Leukemia
Inborn Errors of Metabolism
Bone Marrow Failure Syndromes
Immunodeficiencies
Immunodysregulation Polyendocrinopathy Enteropathy X-linked Syndrome
Transplant of stem cells with CD3+/CD19+ depletion (CliniMACs)
EARLY_PHASE1
Only 25-30% of patients who may benefit from HSCT have a matched related donor. There is a higher rate of complications using cells from an unrelated or partially matched related donor. T cells within the donor cells may cause a complication called graft vs. host disease (GVHD). The goal of this study is to use the CliniMACs device to remove the T cells that cause GVHD, called T cell depletion.
| Study Type : | INTERVENTIONAL |
| Estimated Enrollment : | 100 participants |
| Masking : | NONE |
| Primary Purpose : | TREATMENT |
| Official Title : | Expanded Access Protocol Using CD3+/CD19+ Depleted Unrelated Donor or Related Donor Peripheral Stem Cells |
| Actual Study Start Date : | 2013-12 |
| Estimated Primary Completion Date : | 2027-01 |
| Estimated Study Completion Date : | 2030-01 |
Information not available for Arms and Intervention/treatment
| Ages Eligible for Study: | to 30 Years |
| Sexes Eligible for Study: | ALL |
| Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
RECRUITING
Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States, 19104