Dmitry Rogachev Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology
Moscow, 117997, Russia
NCT Number: NCT02327351
Treatment Study to assess of safety and efficiency of T cells receptor (TCR) alfa beta depleted graft for hematopoietic stem cell transplantation (HSCT) from haploidentical and unrelated donors in patients with primary immunodeficiency diseases
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Notify Me1 month–18 year
All sexes
Interventional
Phase 2 / Phase 3
Moscow, 117997, Russia
Infections, graft versus host diseases (GVHD) and associated morbidity and mortality remains significant problems after unrelated and haploidentical hematopoietic stem sell transplantation (HSCT) in patients with primary immunodeficiency diseases (PID). In this study the hypothesis is that the transplantation of TCR alfa beta depleted peripheral blood stem cells (PBSC) would offers advantages over the use of positively selected CD34+ stem cells in haploidentical HSCT and non-manipulated graft in unrelated HSCT.
The purpose of this study is to evaluate the safety and efficiency of the selective infusion of TCR alfa beta T cell depleted graft in pediatric patients with PID receiving HSCT from haploidentical and unrelated donors.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 1 year after HSCT
The probability of overall survival estimated by the Kaplan-Meier method at 1 year after HSCT
Time frame: 24 months after transplantation
transplant-related mortality estimated with cumulative incidence curve, considering relapse as a competitive risk
Time frame: 12 months after transplantation
incidence of aGVHD II-IV stage estimated with cumulative incidence curve, considering graft rejection and death as competitive risks
Time frame: 1 year after HSCT
incidence of cGVHD estimated with cumulative incidence curve, considering graft rejection and death as competitive risks
Time frame: 2 years after HSCT
Number of participants, who reached immune recovery - CD19+ lymphocytes subsets
Time frame: last follow-up
Percentage of patients with full (more than 90%) donor chimerism among survivals
Time frame: 12 months after transplantation
number of patients with CMV reactivation (detection of any grade of CMV viremia after HSCT)
Federal Research Institute of Pediatric Hematology, Oncology and Immunology
Other
Phase II/III Study of Allogeneic Hematopoietic Stem Cell Transplantation From Unrelated and Haploidentical Donors After TCR Alfa Beta Negative Selection in Pediatric Patients With Primary Immunodeficiency Diseases
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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