MCW Alpha/Beta T-Cell and B-Cell Depletion With Targeted ATG Dosing

Trial Title: MCW Alpha/Beta T-Cell and B-Cell Depletion With Targeted ATG Dosing

NCT ID: NCT05794880

Condition: Leukemia
Acute Myeloid Leukemia in Remission
Myelodysplasia
Acute Lymphoblastic Leukemia in Remission
Chronic Myelogenous Leukemia - Chronic Phase
Chronic Myelogenous Leukemia, Accelerated Phase
Chronic Myelogenous Leukemia With Crisis of Blast Cells
Biphenotypic Acute Leukemia
Lymphoblastic Lymphoma
Burkitt Lymphoma
Burkitt Leukemia
Lymphoma After Relapse
Other Malignant Hematologic Diseases in Remission

Conditions: Official terms:
Burkitt Lymphoma
Lymphoma
Leukemia
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Myeloid
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
Leukemia, Biphenotypic, Acute
Leukemia, Myeloid, Chronic-Phase
Leukemia, Myeloid, Accelerated Phase
Hematologic Diseases

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Device
Intervention name: Magnetic-Activated Cell Sorter (CliniMACS, Miltenyi)
Description: Participants in this study will receive a blood stem cell transplant, which will use an investigational device called the CliniMACs device to remove alpha/beta T cells and B cells from the blood cells collected from the donor. This is called T cell depletion and B cell depletion.
Arm group label: Alpha/Beta T cell depletion (TCD) plus CD19+ depletion

Summary: This is a single arm pilot study for patients with hematologic malignancies receiving unrelated or haploidentical related mobilized peripheral stem cells (PSCs) using the CliniMACS system for alpha/beta T cell depletion plus CD19+ B cell depletion with individualized ALC-based dosing of ATG to study impact on engraftment, GVHD, and disease free survival

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Patient age < 25 years. Both genders and all races eligible. 2. Disease eligibility - Acute myeloid leukemia, primary or secondary - Disease status: MRD negative (flow MRD ≤ 0.1%) - Myelodysplasia - Acute lymphoblastic leukemia - Disease status: MRD negative - Chronic myelogenous leukemia - Disease status: chronic phase, accelerated phase or blast crisis now in second chronic phase - Mixed lineage or biphenotypic acute leukemia- Disease status: MRD negative - Lymphoblastic lymphoma - Disease status: in remission - Burkitt's lymphoma/leukemia - Disease status: in remission - Lymphoma after relapse - Disease status: in remission - Other malignant hematologic diseases in remission (to be approved by PI) 3. Karnofsky Performance Status ≥ 60% for patients 16 years and older and Lansky Play Score ≥ 60 for patients under 16 years of age (Appendix 1) 4. Evaluation of organ status as per MCW BMT SOP 5. Infectious disease criteria: No active untreated infection. Patients with possible fungal infections must have had at least 2 weeks of appropriate anti-fungal antibiotics and be asymptomatic. 6. Signed consent by parent/guardian or able to give consent if ≥18 years. 7. Negative pregnancy test for patients capable of childbearing potential 8. Sexually active patients capable of child-bearing potential must agree to use adequate contraception (diaphragm, birth control pills, injections, intrauterine device [IUD], surgical sterilization, subcutaneous implants, or abstinence, etc.) for the duration of treatment. Sexually active men must agree to use barrier contraceptive for the duration of treatment. Donor Eligibility: 1. Unrelated donor meets National Marrow Donor Program criteria for donation 2. Infectious disease testing 3. MCW BMT procedures apply for determining donor eligibility, including donor screening and testing for relevant communicable disease agents and diseases. 4. Only Peripheral blood stem cells will be used for stem cell source on this study therefore donor must be willing to undergo G-CSF mobilization and stem cell apheresis. Donor matching. High resolution typing at all loci to be performed. 5. Unrelated Donor: a. HLA typing of at least 10 alleles is required. Donor must be matched at 9/10 or 10/10 alleles (HLA A, B, C, DRB1, DQB1).Donor and collection center willing to undergo mobilization and apheresis 6. Haploidentical Related Donor: 1. Haploidentical parent or other related donor: Minimum match level full haploidentical (at least 5/10; HLA A, B, C, DRB1, DQB1 alleles), but use of haploidentical donors with extra matches (e.g. 6, 7, or 8/10) encouraged. Exclusion Criteria: 1. Patients who do not meet disease, organ, or infectious criteria. 2. No suitable donor 3. Pregnant or lactating patients are ineligible as many of the medications used in this protocol could be harmful to unborn children and infants 4. Receiving concomitant chemotherapy, radiation therapy; immunotherapy or other anti-cancer therapy for treatment of disease other than is specified in the protocol. Maintenance or other post-HCT therapy can be considered after discussion with the study PI. 5. Participating in a concomitant Phase 1 or 2 study involving treatment of disease 6. Active malignancy other than eligible disease specified in the protocol. Patients with prior malignancy can be eligible as long as at least 1 year post treatment for that malignancy.

Gender: All

Minimum age: 0 Years

Maximum age: 25 Years

Healthy volunteers: No

Locations:

Facility:
Name: Children's Wisconsin

Address:
City: Milwaukee
Zip: 53226
Country: United States

Status: Recruiting

Contact:
Last name: Meredith Beversdorf, RN

Phone: 414-266-5891
Email: mbeversdorf@childrenswi.org

Investigator:
Last name: Amy Moskop
Email: Principal Investigator

Start date: May 1, 2023

Completion date: May 2032

Lead sponsor:
Agency: Medical College of Wisconsin
Agency class: Other

Source: Medical College of Wisconsin

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05794880