About this trial
The primary objective 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 Institutional Review Board (IRB) approved protocols that utilize CliniMACs technology for T depletion.
Eligibility criteria
Qualifiers
Metabolic storage diseases correctable by HSCT
Bone marrow failure syndromes
Immunodeficiencies/immune dysregulation syndromes
Sickle cell disease or thalassemia
Disqualifiers
Uncontrolled bacterial, viral, or fungal infections
Fully HLA matched sibling donor (fully matched related donors including siblings may be included in special circumstances)
Donor unable to donate peripheral stem cells
Pregnant Females
Trial design
Treatments tested in this trial
- Apha/beta T and CD19+ cell depletion using CliniMACS device