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Pediatric Hematologic MalignanciesPhase 1NCT05011422

Haploidentical Hematopoietic Stem Cell Transplantation With Ex Vivo TCR Alpha/Beta and CD19 Depletion in Pediatric Hematologic Malignancies

A Phase 1 study testing Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs Plus in people with Pediatric Hematologic Malignancies, run by Washington University School of Medicine at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This single arm pilot phase I study with safety run-in is designed to estimate the safety and efficacy of a familial mismatched or haploidentical hematopoietic stem cell transplantation (haplo-HSCT) using a novel graft modification technique (selective αβ-TCR and CD19 depletion). Read more about this study

Who is it for?
Ages Up to 30 years
Conditions the study is for
Pediatric Hematologic Malignancies
What is being tested?
Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs Plus
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteUnited States
Study dates
3 Nov 2022to 31 May 2029
Phase
Phase 1
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 30 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Recipient Inclusion Criteria:

  • Must meet at least one of the following disease criteria:
  • B cell ALL in first remission and any of the following:
  • Persistent flow-based MRD at end-of-consolidation:
  • ≥ 1% for NCI SR ALL
  • ≥ 0.01% for NCI HR ALL
  • TCF3-HLF t(17;19)
  • KMT2A rearranged infant ALL, < 6 months of age and presenting WBC of > 300,000 or poor steroid response (peripheral blasts >= 1000 /uL on day 8 of therapy
  • Other high-risk features not explicitly stated here, after discussion/approval with protocol PI.
  • B cell ALL in second remission and any of the following:
  • Early (<36 months from start of therapy) marrow or combined relapse
  • Late (>36 months from start of therapy) marrow or combined relapse with end-of re-induction flow MRD >= 0.1%
  • Early isolated extramedullary relapse (< 18 months from start of therapy)
  • Any B cell ALL in third or greater remission
  • T cell ALL in first remission
  • End-of consolidation MRD > 0.1%
  • Any T cell ALL in second or greater remission
  • AML in first remission with any of the following high-risk features:
  • MRD ≥ 1% after first induction course
  • MRD ≥ 0.1% after second induction course
  • RPN1-MECOM
  • RUNX1-MECOM
  • NPM1-MLF1
  • DEK-NUP214
  • KAT6A-CREBBP (if >= 90 days at diagnosis)
  • FUS-ERG
  • KMT2A-AFF1
  • KMT2A-AFDN
  • KMT2A-ABI1
  • KMT2A-MLLT1
  • 11p15 rearrangement (NUP98 - any partner gene)
  • 12p13.2 rearrangement (ETV6 - any partner gene)
  • Deletion 12p to include 12p13.2 (loss of ETV6)
  • Monosomy 5/Del(5q) to include 5q31 (loss of EGR1)
  • Monosomy 7
  • 10p12.3 rearrangement (MLLT10b - any partner gene)
  • FLT3/ITD with allelic ratio > 0.1%
  • RAM phenotype as evidenced by flow cytometry: bright CD56+, dim to negative CD45 and CD38 and lack of HLA-DR
  • Other high-risk features not explicitly stated here, after discussion/approval with protocol PI.
  • AML in second or greater remission
  • Mixed phenotype or undifferentiated leukemia in any CR
  • Secondary to therapy-associated leukemia in any CR
  • NK cell lineage leukemia in any CR
  • Myelodysplastic syndrome (MDS)
  • Juvenile myelomonocytic leukemia (JMML)
  • May have undergone a prior hematopoietic stem cell transplant provided one of the criteria in Inclusion Criterion #1 are met AND the patient does not have active GVHD (has been off immunosuppression for at least 3 months).
  • Available familial haploidentical donor.
  • Donor and recipient must be identical at a minimum of one allele of each of the following genetic loci: HLA-A, HLA-B, HLA-Cw, HLA-DRB1, and HLA-DQB1. A minimum of 5/10 match is required and will be considered sufficient evidence that the donor and recipient share one HLA haplotype.
  • No more than 30 years of age
  • Lansky or Karnofsky performance status > 50%
  • Adequate organ function as defined below:
  • Cardiac: LVEF ≥ 40% at rest or SF ≥ 26%
  • Hepatic:
  • Total bilirubin < 3 x IULN for age
  • AST(SGOT)/ALT(SGPT) < 5 x IULN
  • Renal: GFR ≥ 60 mL/min/1.73m2 as estimated by updated Schwartz formula for ages 1-17 years (see Appendix B), 24-hour creatinine clearance, or renal scintigraphy. If GFR is abnormal for age based on updated Schwartz formula, accurate measurement should be obtained by either 24-hour creatinine clearance or renal scintigraphy. Renal function may also be estimated by serum creatinine based on age/gender. A minimum serum creatinine of 2x upper limit of normal is required for inclusion on this protocol.
  • Pulmonary:
  • O2 saturation ≥ 92% on room air without positive pressure support
  • FEV1, FVC, and DLCO ≥ 50% of predicted (for children unable to perform a pulmonary function test, a high-resolution CT chest may be obtained)
  • The effects of these treatments on the developing human fetus are unknown. For this reason, patients of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for 24 months following transplant. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
  • Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Recipient Exclusion Criteria:

  • Available matched related donor. A patient with a matched unrelated donor is eligible if urgent transplantation is required. A prior unrelated donor search is not required for enrollment.
  • Active non-hematologic malignancy. History of other malignancy is acceptable as long as therapy has been complete and there is no evidence of disease.
  • Currently receiving any other investigational agents at the time of transplant.
  • Active CNS or extramedullary disease. History of CNS or extramedullary disease now in remission is acceptable.
  • A history of allergic reactions attributed to compounds of similar chemical or biologic composition to conditioning agents used in the study.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection (bacterial, viral with clinical instability, or fungal), symptomatic congestive heart failure, or unstable cardiac arrhythmia.
  • Presence of significant anti-donor HLA antibodies per institutional standards. Anti-donor HLA Antibody Testing is defined as a positive crossmatch test of any titer (by complement dependent cytotoxicity or flow cytometric testing) or the mean fluorescence intensity (MFI) of any anti-donor HLA antibody by solid phase immunoassay.
  • Presence of a second major disorder deemed a contraindication for HSCT.
  • Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of the start of conditioning.

Donor Eligibility Criteria:

  • The preferred donor should be an adult aged at least 18 years or older. However, in circumstances where no suitable adult donor is available, consideration may be given to a minor donor aged 12 years or older. This exception only applies when all identified, otherwise eligible adult donors meet one or more of the following criteria:
  • Have a medical condition that poses unacceptable risk, including autoimmune disease, infection, hematologic disorder, malignancy, or a pathogenic germline mutation.
  • Have comorbidities that preclude safe administration of granulocyte colony-stimulating factor (G-CSF), placement of a pheresis catheter and/or a pathogenic germline mutation.
  • Served as a donor in prior haploidentical HCT.
  • Significant psychosocial or logistical barriers.
  • Meets the selection criteria as defined by the Foundation for the Accreditation of Hematopoietic Cell Therapy (FACT).
  • Able to understand and willing to sign an IRB-approved written informed consent document (or that of legally authorized representative, if applicable).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Thomas Pfeiffer, M.D. contact

314-273-2070

pthomas@wustl.edu

United States1 site, 1 recruiting
  • Washington University School of Medicine

    St Louis, Missouri, 63110

    Thomas Pfeiffer, M.D., 314-273-2070, pthomas@wustl.edu

    Thomas Pfeiffer, M.D.

    Recruiting

Other trials in United States

About this study

Official title: A Pilot Study of Haploidentical Hematopoietic Stem Cell Transplantation With Ex Vivo TCR Alpha/Beta and CD19 Depletion in Pediatric Hematologic Malignancies

This single arm pilot phase I study with safety run-in is designed to estimate the safety and efficacy of a familial mismatched or haploidentical hematopoietic stem cell transplantation (haplo-HSCT) using a novel graft modification technique (selective αβ-TCR and CD19 depletion).

Being tested
Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs Plus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs PlusDevice

    Once pheresed, the product will be washed to remove platelets and the cell concentration will be adjusted per laboratory and ClinicMACS technology recommendations. It is then labeled using the CliniMACS αβ-TCR Biotin Kit and CD19+ immunomagnetic microbeads. After labeling, the cells are washed to remove unbound microbeads. The partially processed product is loaded on the CliniMACS device where labeled cells are depleted and the negative fraction is eluted off the device. The negative fraction is centrifuged and volume reconstituted to obtain the final product

Study groups in NCT05011422
Study groupRoleWhat they receive
Recipients: ex vivo αβ-TCR/CD19 depleted haplo-hematopoietic stem cell infusion (HSCT)Experimental* Patients will undergo standard of care conditioning regiment prior to HSCT * On Day 0, patients will undergo infusion of the ex vivo αβ-TCR/CD19 depleted haplo-HSCT from a stimulated peripheral stem cell source per institutional standard of care. Patients whose graft has a residual CD20+ count > 1.0 x 10^5 may receive a single infusion of rituximab on Day +1 at a dose of 375 mg/m^2 at provider's discretion.
Receives: Device: Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs Plus
Donors:No interventionDonors who meet the eligibility criteria will be mobilized as per institutional standard practice using G-CSF 10 mcg/kg/day with leukapheresis to take place on Day 5. The target volume for collection is 20 L. Up to 4 days of pheresis are permitted to ensure target collection.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Safety as measured by the number of events occurring within the first 100 days post-transplant

    -Events are death, disease recurrence or progression, and graft failure

    Measured: Through 100 days post-transplant

  2. Engraftment as measured by time to neutrophil count recovery

    Time to neutrophil recovery is defined as the first of 3 measurements on different days when the patient has an absolute neutrophil count of >500/μL after conditioning.

    Measured: From day of transplant (day 0) to 42 days (+/- 14 days) post transplant

  3. Engraftment as measured by time to platelet count recovery

    Time to platelet recovery is defined as the first day of a minimum of 3 measurements on different days that the patient has achieved a platelet count > 50,000/μL AND did not receive a platelet transfusion in the previous 7 days. The exception is the case in which a patient receives platelet transfusions specifically to achieve a higher platelet threshold to allow for an invasive procedure or protection if determined to be at elevated bleeding risk.

    Measured: From day of transplant (day 0) to 75 days (+/- 14 days) post transplant)

  4. Donor cell chimerism as measured by short tandem repeat analysis

    • Can use peripheral blood samples or bone marrow samples
    • The percent of donor-derived cells are sequentially followed.

    Measured: Through day +100

Secondary outcomes (23)
  1. Event free survival (EFS)

    -Death, disease recurrence or progression, and graft failure are considered events

    Measured: At 24 months post transplant

  2. Overall survival (OS)

    Death by any cause is considered an event.

    Measured: At 24 months post transplant

  3. Incidence of grade IV acute GVHD

    -Graded according to the NIH consensus criteria.

    Measured: Weekly through day +100

  4. Incidence of severe chronic GVHD

    -Graded according to the NIH consensus criteria.

    Measured: Day 101 through 24 months

  5. Change in Lansky/Karnofsky performance score

    • Lansky is used for participants <15.99 years of age
    • Karnofsky is used for participants >16.00 years of age

    Measured: Day +100, Day +180, Day +365, and +24 months

  6. Number of pulmonary toxicities

    Measured: Through 24 months

  7. Number of neurologic/neurocognitive toxicities

    Measured: Through 24 months

  8. Number of cardiac toxicities

    Measured: Through 24 months

  9. Number of renal toxicities

    Measured: Through 24 months

  10. Number of hepatic toxicities

    Measured: Through 24 months

  11. Number of metabolic toxicities

    Measured: Through 24 months

  12. Number of thyroid toxicities

    Measured: Through 24 months

  13. Incidence and severity of acute GVHD

    -Graded according to the NIH consensus criteria.

    Measured: From day +14 through Day +100

  14. Incidence and severity of chronic GVHD

    -Graded according to the NIH consensus criteria.

    Measured: From day +101 through 24 months

  15. Number of participants with infections requiring hospitalizations

    Measured: Through 24 months

  16. Immune reconstitution as measured by recovery of absolute neutrophil count

    Measured: Over 24 months

  17. Immune reconstitution as measured by recovery of absolute monocyte count

    Measured: Over 24 months

  18. Immune reconstitution as measured by regain of function of NK cell populations

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via flow cytometry

    Measured: Over 24 months

  19. Immune reconstitution as measured by regain of function of T cell populations

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via flow cytometry

    Measured: Through 24 months

  20. Immune reconstitution as measured by regain of function of B cell populations

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via flow cytometry

    Measured: Through 24 months

  21. Immune reconstitution as measured by regain of function of immunoglobulin G (IgG)

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via serum analysis

    Measured: Over 24 months

  22. Immune reconstitution as measured by regain of function of immunoglobulin A (IgA)

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via serum analysis

    Measured: Over 24 months

  23. Immune reconstitution as measured by regain of function of immunoglobulin M (IgM)

    • Immune reconstitution is defined as regain of function of donor-derived immunogenic cells. Immune reconstitution is to be measured by recovery of individual cellular compartments
    • Via serum analysis

    Measured: Over 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Aug 2021
  2. Study start3 Nov 2022
  3. Primary completion31 May 2029 (estimated)
  4. Study completion31 May 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05011422
Sponsor's protocol ID
202203051
Status last verified
Aug 2026
First submitted
11 Aug 2021
Last updated
19 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Ex Vivo T-cell receptor alpha-beta and CD19+ Depletion using CliniMACs Plus in people with Pediatric Hematologic Malignancies, run by Washington University School of Medicine at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 19 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Thomas Pfeiffer, M.D. (314-273-2070, pthomas@wustl.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Safety as measured by the number of events occurring within the first 100 days post-transplant (time frame: Through 100 days post-transplant). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Aug 2026.

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