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CD19 PositivePhase 1NCT07896213

Metabolically Fit CD19 CAR T Cells With CD34 Selection Markers in Adults With CD19-Positive B-Cell Acute Lymphocytic Leukemia

A Phase 1 study testing Fludarabine, Cyclophosphamide and Levetiracetam in people with CD19 Positive and B-ALL, run by Medical University of South Carolina at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this trial is to determine safe dosing of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL). Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Fludarabine, Cyclophosphamide and Levetiracetam
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
1 siteUnited States
Study dates
1 Nov 2026to 21 Dec 2034
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

An individual must meet all of the following criteria to be eligible for enrollment:

  1. Age 18 years or older.
  2. Willing and able to give written, informed consent to the current study.
  3. ECOG performance status of 0, 1 or 2.
  4. Relapsed or refractory CD19-positive B-ALL defined as one of the following:
  5. Primary refractory disease (not achieving CR after two cycles of induction chemotherapy).
  6. Relapse after prior complete remission.
  7. Relapsed or refractory disease after allogeneic transplant provided CAR-T infusion occurs at least 2 months after the stem cell transplant. NOTE: In patients treated with blinatumomab, CD19 expression on leukemic blasts must be confirmed after blinatumomab therapy has been stopped.
  8. Cohort-specific inclusion criteria:
  9. Cohort Ia: Relapsed/Refractory B-ALL i. Presence of ≥5% blasts in BM at screening, or with isolated extramedullary disease (EMD) (including isolated CNS disease), with or without MRD in the BM ii. Patients with Philadelphia chromosome positive ALL (Ph+ ALL) are eligible if they are intolerant to or have failed two lines of any TKI or one line of second-generation TKI, or if TKI therapy is contraindicated.
  10. Cohort Ib: B-ALL in remission with measurable residual disease i. MRD-positive defined as ≥10-6 and <5% blasts in the BM at screening. ii. Patients with Philadelphia chromosome positive ALL (Ph+ ALL) are eligible if they are intolerant to or have failed two lines of any TKI or one line of second-generation TKI, or if TKI therapy is contraindicated.
  11. Cohort Ic: B-ALL in remission, indicated but ineligible for or unwilling to undergo allogenic transplant i. B ALL in MRD negative remission, being considered (typically for high-risk B-ALL) for, but ineligible for allogeneic stem cell transplantation due to organ dysfunction, socioeconomic factors or other extraneous reasons as determined by the transplant physician. ii. B ALL in MRD negative remission, being considered (typically for high-risk B-ALL) for, but unwilling to undergo allogeneic stem cell transplantation for patient's personal reasons.
  12. For females of childbearing potential (defined as <24 months after last menstruation or not surgically sterile), a negative serum or urine pregnancy test must be documented at screening, prior to pre-conditioning and confirmed before receiving the first dose of study treatment.
  13. For females who are not postmenopausal (<24 months of amenorrhea) or who are not surgically sterile (absence of ovaries and/or uterus), two methods of contraception comprising of one highly effective method of contraception together with a barrier method must be used during the treatment period and for at least 12 months after the last dose of study treatment. They must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for 12 months after receiving the last dose of study drug (please refer to Appendix F).
  14. For males, it must be agreed that two acceptable methods of contraception are used (one by the patient - usually a barrier method, and one highly effective method by the patient's partner as defined in Appendix F) during the treatment period and for at least 12 months after the last dose of study treatment and that sperm will not be donated during the treatment period and for at least 12 months after the last dose of study treatment.
  15. Adequate renal, hematologic, hepatic, pulmonary, and cardiac function defined as:
  16. Serum alanine aminotransferase/aspartate aminotransferase ≤3 x ULN.
  17. Creatinine clearance (as estimated by Cockcroft-Gault) ≥50 cc/minute.
  18. Absolute lymphocyte count (ALC) ≥150 cells/mm3.
  19. Total bilirubin ≤1.5 x ULN, except in patients with Gilbert's syndrome who must have normal direct bilirubin.
  20. Baseline oxygen saturation >92% on room air.
  21. Left ventricular ejection fraction (LVEF) ≥ 45%, no evidence of clinically significant pericardial effusion as determined by an ECHO.

A second CAR-T cell infusion may be considered if the following criteria are met:

  1. Patient to receive subsequent cell infusion did not experience unacceptable toxicity from the first infusion. Any toxicity (regardless of causality) after the previous CD19-CD34t metabolically programmed CAR-T cell infusion must resolve such that participants meet all the initial eligibility criteria. AND one or more of the following criteria are also met:
  2. Loss of B-cell aplasia past 6 months from the date of original CAR-T infusion, defined as either or both:
  3. CD19+ cells ≥3% of peripheral lymphocytes and absolute CD19 count ≥50/μL.
  4. Patients with CD19+ cells ≥3% of peripheral lymphocytes, but absolute CD19 count <50 are required to have at least two sets of lymphocyte subsets drawn to confirm stable to up trending absolute CD19 counts.
  5. Relapse or refractory disease, defined as either or both:
  6. Emergence or persistence of CD19 expressing MRD positive disease at any time past original CAR-T infusion past 4 weeks after original infusion.
  7. Frank CD19 positive relapse or refractory disease past 4 weeks after original infusion.

An individual will be excluded from the study if any of the following apply:

  1. Diagnosis of chronic myelogenous leukemia in lymphoid blast crisis.
  2. Presence of current CNS 3 disease. Prior CNS 3 disease is allowed if they are treated with residual CNS 1/2 disease.
  3. Females who are pregnant or lactating.
  4. Receipt of live vaccine within 6 weeks prior to enrollment.
  5. Prior CAR-T or Gene Therapy: Previous treatment with any CD19-directed CAR-T cell therapy. (Rationale: prior CAR-T could affect CD19 antigen status and immune response; also, to isolate the effect of this investigational product. However, prior CD19 CAR-T is allowed if it was more than 6 months prior to enrollment and the patient has confirmed CD19+ relapse).
  6. Uncontrolled Infection: Known active infection including:
  7. Positive blood cultures for bacteria or fungi with signs of systemic infection that are not controlled.
  8. Active tuberculosis.
  9. Opportunistic infections (e.g., Pneumocystis pneumonia, CMV viremia) that are not resolved.
  10. Fever of unknown origin is a caution; prior to lymphodepletion, a complete evaluation to rule out infection should be done and the treating physician must agree that it is okay to proceed.
  11. Concurrent Malignancy: Another active malignancy requiring therapy or that is expected to limit survival to <2 years, except certain low-risk cancers (e.g., treated localized prostate cancer on surveillance, adequately treated basal cell carcinoma of skin).
  12. Autoimmune Disorder: Active autoimmune disease requiring systemic immunosuppressive therapy (e.g. lupus, multiple sclerosis, etc.) especially if the disease or its treatment could be worsened by CAR-T (because steroids or immunosuppressants to control autoimmunity could interfere with CAR-T function, and autoimmunity could flare with immune activation).
  13. Allogeneic Transplant History: Prior allogeneic hematopoietic stem cell transplant with active graft-versus-host disease (GVHD) of any grade.
  14. Significant Co-morbid Conditions: For example:
  15. Unstable angina, myocardial infarction within 6 months, or uncontrolled cardiac arrhythmia.
  16. No clinically significant signs or symptoms of cardiac dysfunction defined as symptoms consistent with NYHA CHF classification III or IV.
  17. Acute neurological toxicity > Grade 1 (with the exception of peripheral sensory neuropathy).
  18. Stroke or seizure disorder not controlled on medication.
  19. Interstitial lung disease requiring supplemental oxygen.
  20. Any condition that the investigator deems would make the patient unsuitable (e.g., severe frailty or logistic inability to comply with frequent monitoring).
  21. Concurrent Therapy: Use of systemic corticosteroids above a physiologic replacement dose (equivalent to >10 mg prednisone daily) within 7 days prior to leukapheresis or planned need for such steroids.

NOTE: Patients who require steroids for disease control must be tapered off before T cell collection, since steroids can impair T cell function for manufacturing and may preclude CAR T expansion after infusion. If emergent steroid use is needed for an indication like brain metastases, patient should be deferred.

  1. Similarly, any other anti-cancer therapy (chemotherapy, targeted agents, investigational drugs) must be washed out before lymphodepletion (timeframe depends on drug, typically 2 weeks or 5 half-lives, whichever is longer).
  2. Radiation must have stopped ≥ 2 weeks prior to collection.
  3. New requirement for oxygen therapy.

A second CAR-T cell infusion will not be considered if any of the following criteria are met:

  1. All above exclusion criteria apply to a second infusion.
  2. Grade 3 or higher CRS/ICANS with original infusion at dose level -1.

Trial locations and contacts

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

HCC Clinical Trials Office contact

843-792-9321

hcc-clinical-trials@musc.edu

United States1 site
  • Medical University of South Carolina Hollings Cancer Center

    Charleston, South Carolina, 29425

    HCC Clinical Trials Office, 843-792-9321, hcc-clinical-trials@musc.edu

Other trials in United States

About this study

Official title: A Phase 1B Safety and Feasibility Study of Metabolically Fit CD19 Chimeric Antigen Receptor (CAR)-T Cells With CD34 Selection Markers in Adult Patients With CD19 Positive B-Cell Acute Lymphocytic Leukemia

The goal of this trial is to determine safe dosing of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL).

The main questions it aims to answer are to determine the maximum tolerated dose (MTD) of CD19-CD34t metabolically programmed CAR-T cell therapy, to assess the safety of CD19-CD34t metabolically programmed CAR-T cell therapy, and to determine the feasibility of manufacturing CD19-CD34t metabolically programmed CAR-T cell therapy within 15% of the target dose.

Read the detailed description

This is an open-label, single-center phase Ib de-escalation safety and feasibility study in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL). The trial will evaluate the safety of autologous peripheral blood mononuclear cell (PBMC) obtained by leukapheresis and then transduced with CD19-CD34t CAR retroviral vector followed by conditioning for a metabolically programmed (TH1/TH17) enhanced CAR-T cell product. The design will follow a 3+3+3 de-escalation design. The starting dose (dose level 1 [DL1]) is 2 x 106 transduced T cells/kg (±15%), based on the RP2D from NCT05702853. A step-down dose (dose level -1 [DL-1]) of 1.4 x 106 transduced T cells/kg (±15%) will be evaluated for safety if DL1 is too toxic. DL1 and DL-1 have demonstrated exceptional safety with therapeutic exposure in the ongoing lymphoma trial (NCT05702853) of this same investigational CAR-T product.

Participants will receive a lymphodepleting preparative regimen of fludarabine and cyclophosphamide followed by infusion of CD19-CD34t metabolically programmed CAR transduced T cells on day 0. Participants will be evaluated sequentially after treatment for toxicity, antitumor effects, and for persistence/expansion of CAR in blood samples and functionality of transduced T cells.

Being tested
Fludarabine, Cyclophosphamide, Levetiracetam, CD19 CAR-T cells
Medical subject headings
Burkitt Lymphoma

What participants receive

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

  • FludarabineDrug

    30 mg/m2, IV over 30-60 minutes +/- 10 minutes after cyclo- phosphamide infusion, Days -5, -4, -3

  • CyclophosphamideDrug

    500 mg/m2, IV over 30-60 minutes +/- 10 minutes before Fludarabine, Days -4, -3

  • LevetiracetamDrug

    (500-750 mg BID) is administered prophylactically starting on Day 0.

  • CD19 CAR-T cellsDrug

    Autologous CD19 CAR-T cells expressing truncated CD34 (CD34t) administered intravenously following lymphodepleting chemotherapy. Participants receive either Dose Level 1 or Dose Level -1 according to the protocol-defined dose de-escalation design.

Study groups in NCT07896213
Study groupRoleWhat they receive
Cohort 1a - Relapsed/Refractory B-ALLExperimentalAdult patients with relapsed or refractory CD19-positive B-cell acute lymphoblastic leukemia (B-ALL) receiving lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy.
Receives: Drug: Fludarabine; Drug: Cyclophosphamide; Drug: Levetiracetam; Drug: CD19 CAR-T cells
Cohort 1b - B-ALL in remission with measurable residual diseaseExperimentalAdult patients with CD19-positive B-cell acute lymphoblastic leukemia in remission with measurable residual disease (MRD) receiving lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy.
Receives: Drug: Fludarabine; Drug: Cyclophosphamide; Drug: Levetiracetam; Drug: CD19 CAR-T cells
Cohort 1c - B-ALL in Remission, Indicated but Unable to Undergo Allogeneic TransplantExperimentalAdult patients with CD19-positive B-cell acute lymphoblastic leukemia in MRD-negative remission who are indicated for but unwilling to undergo or ineligible for allogeneic stem cell transplantation due to organ dysfunction, socioeconomic factors, or other reasons determined by the transplant physician. These patients receive lymphodepleting chemotherapy followed by CD19-CD34t metabolically programmed CAR-T cell therapy.
Receives: Drug: Fludarabine; Drug: Cyclophosphamide; Drug: Levetiracetam; Drug: CD19 CAR-T cells
Retreatment Cohort - Patients from cohorts 1a - 1c who are retreatedExperimentalPatients previously treated in Cohort 1a, Cohort 1b, or Cohort 1c who meet protocol-defined eligibility criteria for retreatment and receive lymphodepleting chemotherapy followed by a second infusion of CD19-CD34t metabolically programmed CAR-T cells.
Receives: Drug: Fludarabine; Drug: Cyclophosphamide; Drug: Levetiracetam; Drug: CD19 CAR-T cells

What is being measured

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

  1. Determine the maximum tolerated dose (MTD) of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL).

    The frequency and percentage of dose limiting toxicities (DLTs) summarized by dose level and overall.

    Measured: 28 days

  2. Assess the safety of CD19-CD34t metabolically programmed CAR-T cell therapy

    The frequency and percentage of adverse events (AEs), serious adverse events (SAEs), and treatment-emergent adverse events (TEAEs) summarized by dose level and overall.

    Measured: 28 days

  3. Determine the feasibility of manufacturing CD19-CD34t metabolically programmed CAR-T cell therapy within 15% of the target dose.

    Proportion of patients for whom their CAR-T cellular product is prepared within 15% of the target dose. Feasibility will be evaluated for initial and second infusion separately.

    Measured: 28 days

Secondary outcomes (10)
  1. Overall remission rate (ORR)

    Proportion of patients achieving a complete remission (CR) or a complete remission with incomplete recovery (CRi) for Cohort 1a.

    Measured: 28 days

  2. Rate of MRD-negative CR in bone marrow

    by NGS and/or flow cytometry in Cohort 1a, Cohort 1b, Retreatment cohort w/re-emergence of MRD)

    Measured: 28 days

  3. Stem cell transplantation prior to leukemia relapse

    Proportion of patients undergoing stem cell transplantation prior to leukemia relapse in Cohort 1a, Cohort 1b, Retreatment cohort w/relapse of CD19+ ALL

    Measured: up to 5 years or a disease progression

  4. Rate of B cell aplasia reinduction

    Reinduction of B cell aplasia retreatment cohort w/loss of B cell aplasia

    Measured: up to 5 years or a disease progression

  5. ORR after 2nd infusion

    Proportion of patients achieving a complete remission (CR) or a complete remission with incomplete recovery (CRi) for Retreatment cohort w/relapse of CD19-positive ALL

    Measured: up to 5 years or disease progression

  6. Rate of CR/CRi without stem cell transplantation or other subsequent therapy

    Proportion of patients in CR/CRi without stem cell transplant or other subsequent therapy at 6-, 12-, and 24-months following CAR-T infusion for Cohort 1a, Cohort 1b, Cohort 1c

    Measured: up to 24 months

  7. Rate of CD19-negative relapse

    Incidence of CD19 negative relapse for Cohort 1a, Cohort 1b, Cohort 1c

    Measured: up to 5 years or disease progression

  8. Progression-free survival (PFS)

    the time interval from first CAR-T cell infusion to disease progression, relapse, or death due to any cause in Cohort 1a, Cohort 1b, Cohort 1c

    Measured: up to 5 years or disease progression, relapse, or death

  9. Duration of response (DOR)

    the time interval from first documented response to disease progression or death due to any cause. DOR is defined only among patients who experience a response to the CAR-T cell therapy Cohort 1a, Cohort 1b, Cohort 1c

    Measured: up to 5 years or response to disease progression or death

  10. Overall survival (OS)

    the time interval from first CAR-T cell infusion to death due to any cause in Cohort 1a, Cohort 1b, Cohort 1c

    Measured: up to 5 years or death

Timeline

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

  1. First posted26 Oct 2026
  2. Study start1 Nov 2026 (estimated)
  3. Primary completion21 Dec 2033 (estimated)
  4. Study completion21 Dec 2034 (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
Sequential
Masking
None (open label)
Enrolment
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07896213
Sponsor's protocol ID
104236
Status last verified
Oct 2026
First submitted
19 Oct 2026
Last updated
26 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Fludarabine, Cyclophosphamide and Levetiracetam in people with CD19 Positive and B-ALL, run by Medical University of South Carolina 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: opening soon, as of the sponsor's last update on 26 Oct 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 HCC Clinical Trials Office (843-792-9321, hcc-clinical-trials@musc.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Determine the maximum tolerated dose (MTD) of CD19-CD34t metabolically programmed CAR-T cell therapy in adult patients with CD19-positive B-cell acute lymphocytic leukemia (B-ALL). (time frame: 28 days). The study lists 3 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 26 Oct 2026.

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