An expanded access record providing CliniMACS® CD34 TCR Alpha/Beta in Transplant-Related Disorder and GVH - Graft Versus Host Reaction, sponsored by Victor Aquino. Available at 1 site in United States. Open to participants aged Up to 21 Years. Per ClinicalTrials.gov, last updated 2025-10-14.
Sponsored by Victor Aquino · Expanded access
The protocol is designed to provide access to patients to the Clinimacs® CD34 TCRαβ system to prepare cells for an unlabeled indication using an HLA-compatible related or unrelated donor for allogenic transplant.
Allogeneic hematopoietic stem cell transplant (HSCT) is the only known curative therapy for a variety of non-malignant and malignant disorders1-4. Only about 25% of patients have an HLA-matched sibling and in about 16-75% (depending on ethnicity), a 10/10 HLA-matched unrelated donor can be identified. Engraftment failure is a dynamic complex process that may occur with this product due to unbalanced depletion of T-cells between recipient and donor, not only due to low number of CD34 cells. The use of mis-matched or haploidentical donors is associated with a higher risk of post-transplant mortality due to the development of severe graft versus host disease, graft failure and the development of infection due to the use of immunosuppression or T cell depletion. A total of 10 patients will be enrolled. The patients will be divided into 2 strata (haploidentical 7, unrelated donor 3).
This is the only study on the registry with Victor Aquino as lead sponsor.
Counted across the registry records on this site, refreshed daily.
Recipient Inclusion Criteria:
Donor Inclusion Criteria:
Must meet appropriate screening/eligibility requirements:
Recipient Suitability:
- Adequate organ functioning as demonstrated by:
Donor Suitability:
- Allowed Donor Sources
Recipient and Donor Exclusion Criteria:
CliniMACS System uses an automated antibody/magnetic beads column system that allows efficient depletion of TCRαβ and CD19+ cells without relevant loss of cell viability. Hematopoietic stem cells are retained in sufficient numbers to permit engraftment and hematopoietic reconstitution. Humanitarian Exemption IDE approval has been obtained for CD34+ cell selection as a method of T-cell depletion.
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