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Completed

NCT Number: NCT02327351

TCR Alpha/Beta Depletion for HSCT From Haploidentical and Unrelated Donors in the Treatment of PID

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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Key information

Age range

1 month–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Dmitry Rogachev Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology

Moscow, 117997, Russia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged ≥ 1 months and < 19 years
  • Patients diagnosed with Primary Immunodeficiency Diseases eligible for an allogeneic transplantation and lacking a related HLA-matched donor
  • Lansky/Karnofsky score > 40, WHO > 4
  • Signed written informed consent

Exclusion criteria

  • Dysfunction of liver (ALT/AST > 5 times normal value, or bilirubin > 3 times normal value), or of renal function (creatinine clearance < 30 ml / min)
  • Severe cardiovascular disease (arrhythmias requiring chronic treatment, congestive heart failure or left ventricular ejection fraction <40%)
  • Serious concurrent uncontrolled medical disorder
  • Pregnant or breast feeding female patient
  • Lack of parents' informed consent.

Treatment and study plan

Biological: TCR alfa beta T cell depletion

Other

Primary outcomes

  1. Overall Survival

    Time frame: 1 year after HSCT

    The probability of overall survival estimated by the Kaplan-Meier method at 1 year after HSCT

Secondary outcomes

  1. Transplant Related Mortality (TRM)

    Time frame: 24 months after transplantation

    transplant-related mortality estimated with cumulative incidence curve, considering relapse as a competitive risk

  2. Acute Graft Versus Host Diseases (аGVHD)

    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

  3. Chronic Graft Versus Host Diseases (cGVHD)

    Time frame: 1 year after HSCT

    incidence of cGVHD estimated with cumulative incidence curve, considering graft rejection and death as competitive risks

  4. Cellular Immunological Reconstitution

    Time frame: 2 years after HSCT

    Number of participants, who reached immune recovery - CD19+ lymphocytes subsets

  5. Percentage of Patients With Full Donor Chimerism

    Time frame: last follow-up

    Percentage of patients with full (more than 90%) donor chimerism among survivals

  6. Viral Infections After Transplant

    Time frame: 12 months after transplantation

    number of patients with CMV reactivation (detection of any grade of CMV viremia after HSCT)

Sponsors and collaborators

Lead sponsor

Federal Research Institute of Pediatric Hematology, Oncology and Immunology

Other

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2017
Study completion
2018
First posted
Dec 30, 2014
Registry last updated
Feb 26, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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