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NCT Number: NCT04099966

AlloSCT for Malignant and Non-malignant Hematologic Diseases Utilizing Alpha/Beta T Cell and CD19+ B Cell Depletion

Children, adolescents, and young adults with malignant and non-malignant conditionsundergoing an allogeneic stem cell transplantation (AlloSCT) will have the stem cells selected utilizing α/β CD3+/CD19+ cell depletion. All other treatment is standard of care.

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Key information

About this study

Patients wiith selected malignant or non-malignant conditions meeting eligibility criteria will be enrolled on this study. Patients will receive one of either full intensity, reduced intensity, or reduced toxicity conditioning appropriate based on disease, disease status, organ function and performance status and will undergo α/β T-cell and CD 19+ B cell depleted alloSCT.

Patients will be following for engraftment, chimerism, immune reconstitution, GVHD and QOL.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ALL:ALL high risk including one or more of the following: (t(9;22) or 11q23 chromosomal abnormality, primary induction failure (<15% blasts at time of registration), mixed phenotype acute leukemia (MPAL), persistent MRD (<0.01% by flow or persistent abnormal karyotype detected by cytogenetics) or hypodiploidy (44 chromosomes)) in first remission ' ALL in second remission and beyond;
  • AML: History of AML induction/reinduction Failure (<15% blasts at time of registration); AML in CR1 with poor cytogenetics (i.e. 12p, 5a, -7, FLT3 mutation/duplication, t(9;11) and others); AML with persistent minimal residual disease (MRD) in CR1(<0.01% on flow or persistent abnormal karyotype detected by cytogenetics); AML CR2 or beyond; AML in refractory relapse but ≤15% bone marrow leukemia blasts; Therapy-related AML
  • High Risk Myelodysplastic syndrome (MDS) 4 Lymphoma: Hodgkin (HL) or Non-Hodgkin (NHL): HL or NHL in induction failure; HL or NHL in PR1 or PR2 ; HL or NHL in CR2 or subsequent remission
  • Bone marrow failure syndromes: Kostmann syndrome refractory or intolerant to granulocyte colony-33stimulating factor; Diamond-Blackfan anemia refractory or intolerant to corticosteroids and/or cyclosporine'; amegakaryocytic thrombocytopenia 6. Sickle Cell Disease (Homozygous Hemoglobin S Disease, or Hemoglobin S β 0/+ thalassemia, or Hemoglobin SC Disease) 7. age 0-30 years 8. adequate organ function

Exclusion criteria

  • Females who are pregnant or breast-feeding are not eligible.
  • Patients with documented uncontrolled infection at the time of study entry are not eligible.
  • Karnofsky/Lansky (age appropriate) Performance Score <60
  • Demonstrated lack of compliance with medical care
  • Patients who have received allogeneic HSCT within 6 months, unless being done as a boost.
  • Patients with active <Grade 2 GVHD.

Treatment and study plan

alpha beta depletion

Drug

donor cells will be collected and subsequently undergo α/β CD3+/CD19+ cell depletion.

Other names: α/β CD3+/CD19+ cell depletion

Primary outcomes

  1. incidence of adverse events related to administration of α/β CD3+/CD19+ cell depleted stem cells

    Time frame: 1 year

    patients will be monitored for any adverse events related to administration of α/β CD3+/CD19+ cell depleted stem cells

Secondary outcomes

  1. incidence of hematpoitic engraftment following Allogeneic stem cell transplantation (AlloSCT) utilizing α/β CD3+/CD19+ cell depletion

    Time frame: 1 year

    patients will have routine chimerism performed to monitoring engraftment of donor cells

  2. incidence of GVHD following Allogeneic stem cell transplantation (AlloSCT) utilizing α/β CD3+/CD19+ cell depletion

    Time frame: 1 year

    patients will be monitored post transplant for signs of acute and chronic GVHD

Study contacts

Contact information is provided by the study sponsor or research team.

Lauren Harrison, RN

CONTACT

[email protected]

6172857844

Mitchell S Cairo, MD

CONTACT

[email protected]

9145942150

Sponsors and collaborators

Lead sponsor

Mitchell Cairo

Other

Registry information

Official study title

Allogeneic Stem Cell Transplantation for Malignant and Non-malignant Hematologic Diseases Utilizing Alpha/Beta T Cell and CD19+ B Cell Depletion - NYMC 588

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Sep 23, 2019
Registry last updated
Aug 8, 2025

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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