B-AllPhase 1NCT07572136
Anti-CRLF2-R/TSLPR Chimeric Antigen Receptor T Cells (TSLPR-CART) in Participants With Recurrent or Refractory CRLF2-R/TSLPR-Overexpressing B-Cell Acute Lymphoblastic Leukemia (B-ALL)
A Phase 1 study testing TSLPR-CART, Cyclophosphamide and Fludarabine in people with B-All and Acute Lymphoblastic Leukemia, run by National Cancer Institute (NCI) at 1 site in United States.
Trial summary
Background: B-cell acute lymphoblastic leukemia (B-ALL) is a type of blood cancer. Some people with B-ALL have a gene mutation that makes the disease hard to treat. The mutation causes cancer cells to make too much of a protein called thymic stromal lymphopoietin receptor (TSLPR). Read more about this study
- Who is it for?
- Ages 18 to 120 years
- Conditions the study is for
- B-All, Acute Lymphoblastic Leukemia
- What is being tested?
- TSLPR-CART, Cyclophosphamide and Fludarabine
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 57 participants
- Where
- 1 siteUnited States
- Study dates
- 28 Oct 2026to 30 Jun 2032
- Phase
- Phase 1
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 to 120 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Documentation of pathologic confirmation of a diagnosis of B-Cell acute lymphoblastic leukemia (ALL).
- TSLPR+ expression must be detected on >=80% of the malignant cells by NSR device. Note: TSLPR+ expression does not need to be repeated by NSR device if there is a documentation of TSLPR surface expression by flow cytometry from a Clinical Laboratory Improvement Amendments (CLIA) approved laboratory.
- Participants must have a disease that is relapsed or refractory after initial systemic therapy and at least one salvage treatment, and must either be ineligible for, cannot access in a timely manner, or declined alternative curative options (including commercial CAR Tcell constructs*, and/or have relapsed after allogeneic HSCT).
- Individuals that are CD19 positive will be considered for this study, However, these individuals should be ineligible for, unable to obtain in a timely manner, cannot access, unwilling to undergo, or have failed prior FDA approved CD19 CAR constructs.
- Participants must have measurable or evaluable disease at the screening, defined by any evidence of MRD or positron emission tomography (PET)-avid extramedullary disease
- Age >= 18 years
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- Clinical performance status: Karnofsky >= 50%. Participants who are unable to walk because of paralysis, but who are upright in a wheelchair will be considered ambulatory for the purpose of calculating the performance score.
- Participants must have adequate organ and marrow function as defined below:
- Leukocytes >= 750/mcL*
- Platelets >= 50,000/mcL*
- Total bilirubin <= 2 x upper limit of normal (ULN) (except in the case of participants with documented Gilbert s disease > 3 X ULN)
- Aspartate Aminotransferase (AST)/Alanine Aminotransferase (ALT) <= 5 X institutional ULN
- Creatinine < 1.5X ULN OR Creatinine clearance >= 60 mL/min/1.73m^2 for participants with creatinine levels above max listed above
- A participant will not be excluded because of pancytopenia >=Grade 3 if it is due to underlying bone marrow involvement by leukemia
- Cardiac function: left ventricular ejection fraction (LVEF) >=45% or fractional shortening >= 28%, and no clinically significant electrocardiogram (EKG) findings
- Pulmonary Function: Baseline oxygen saturation > 92% on room air at rest without oxygen supplementation
- Participants with the following central nervous system (CNS) status are eligible:
- CNS 1, defined as absence of blasts in CSF on cytospin preparation, regardless of the number of WBCs;
- CNS 2, defined as presence of < 5/mcL WBCs in CSF and cytospin positive for blasts, or > 5/mcL WBCs but negative by Steinherz/Bleyer algorithm:
- CNS 2a: < 10/mcL red blood cells (RBCs); < 5/mcL WBCs and cytospin positive for blasts;
- CNS 2b: >=10/mcL RBCs; < 5/mcL WBCs and cytospin positive for blasts;
- CNS 2c: >=10/mcL RBCs; >= 5/mcL WBCs and cytospin positive for blasts but negative by Steinherz/Bleyer algorithm.
- Contraception:
- Women of child-bearing potential (WOCBP) must agree to use a highly effective contraception (hormonal, intrauterine device [IUD], surgical sterilization, abstinence) at the study entry and up to 12 months after the last dose of combined chemotherapy. Note: WOCBP is defined as any individual who has experienced menarche and who has not undergone successful surgical sterilization or who is not postmenopausal.
- Men able to father a child must agree to use an effective method of contraception (barrier, surgical sterilization, abstinence) at the study entry and for 4 months after the last dose of study drugs. We also will recommend men ask their partners to be on highly effective birth control (hormonal, IUD, surgical sterilization). Men able to father a child must not freeze or donate sperm within the same period.
- Nursing participants must be willing to discontinue nursing from study treatment initiation through 1 month after the last dose of the study drug(s).
- Ability and willingness of participant or Legally Authorized Representative (LAR) to co-enroll on 15-C-0028: Follow-up Evaluation for Gene-Therapy Related Delayed Adverse Events after Participation in Pediatric Oncology Branch Clinical Trials.
- Participant or LAR must understand and sign a written informed consent.
Who cannot join
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- Recurrent or refractory leukemia limited to isolated testicular or isolated CNS disease
- CNS 3 disease including participants with radiologically detected active CNS lymphoma, or participants who have cranial nerve palsy from active CNS leukemia. Note: Chronic complications of prior CNS disease are not exclusionary in the absence of active disease (e.g., blindness from prior ocular CNS disease or persistent cranial nerve palsy)
- Hyperleukocytosis (>=50,000 blasts/mcL)
- Positive serum or urine beta-human chorionic gonadotropin (beta-HCG) pregnancy test performed in WOCBP at screening.
- Washout criteria (time prior to apheresis or prior to start of LD if apheresis is not done on this protocol):
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- Therapy: Systemic chemotherapy, antineoplastic investigational agents, or antibody-based therapies, any investigational therapy
- Washout: >= 2 weeks
- Exceptions: 6 weeks for clofarabine or nitrosoureas No washout for prior intrathecal chemotherapy, steroid therapy, hydroxyurea (no dose increases within prior 2 weeks) or ALL maintenance type chemotherapy (vincristine, 6- mercaptopurine, oral methotrexate, or a tyrosine kinase for participants with Ph+ or Ph-like ALL) provided there is recovery from any acute toxic effects.
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- Therapy: Radiation therapy
- Washout: >= 3 weeks
- Exceptions: No time restriction with radiation therapy if the volume of bone marrow treated is less than 10% and the participant has measurable/evaluable disease outside the radiation window.
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- Therapy: History of allogeneic HSCT
- Washout: >=100 days since HSCT; >=30 days since completion of immunosuppression; >=6 weeks since donor lymphocyte infusion (DLI)
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- Therapy: History of prior CAR therapy or other adoptive cell therapies
- Washout: > 30 days post infusion
- Time between prior therapy and apheresis or prior to start of LD if apheresis is not done on this protocol.
- Human immunodeficiency virus (HIV) infection, as measured by seropositivity for HIV antibody.
- Hepatitis B virus (HBV) infection, as measured by positivity for hepatitis B surface antigen (HbsAg).
- Hepatitis C virus (HCV) infection, as measured by seropositivity for hepatitis C.
- Active second malignancy with the exception of in situ carcinoma of the cervix, unless the tumor was treated with curative intent at least two years previously and participant is in remission.
- History of severe, immediate hypersensitivity reactions attributed to compounds of similar chemical or biologic composition to any agents used in study or in the manufacturing of the cells.
- Evidence of active graft-versus- host disease (GVHD).
- Uncontrolled, symptomatic, intercurrent illness or social situations as evaluated by medical history, physical exam, and laboratory evaluations that would limit compliance with study requirements or would pose an unacceptable risk to the participant.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
National Cancer Institute Referral Office, 888-624-1937, ncimo_referrals@mail.nih.gov
About this study
Official title: Phase I Dose Escalation Study of Anti-CRLF2-R/TSLPR Chimeric Antigen Receptor T Cells (TSLPR-CART) in Participants With Recurrent or Refractory CRLF2-R/TSLPR-Overexpressing B-cell Acute Lymphoblastic Leukemia (B-ALL)
Background:
B-cell acute lymphoblastic leukemia (B-ALL) is a type of blood cancer. Some people with B-ALL have a gene mutation that makes the disease hard to treat. The mutation causes cancer cells to make too much of a protein called thymic stromal lymphopoietin receptor (TSLPR). Chimeric antigen receptor (CAR) T cell therapy is a treatment that takes immune cells (T cells) from a person s body and modifies them to attack specific proteins. Researchers want to test whether TSLPR-CART cells can be given safely to adults with forms of B-cell leukemia, and to learn whether the treatment may help fight these cancers.
Read more
Objective:
To test TSLPR-CART in people with B-ALL.
Eligibility:
People aged 18 years and older with B-ALL that did not respond or returned after treatment. They must have TSLPR on their B-ALL.
Design:
Participants will be screened. They will have imaging scans and tests of their heart function. Samples will be taken from their bone marrow. They will have a lumbar puncture: A needle will be inserted into their back to collect a sample of the fluid around the spinal cord.
Participants will undergo leukapheresis: Blood will be taken from their body through a tube. The blood will pass through a machine that separates out the T cells. The remaining blood will be returned to the body through a different tube. The T cells will be used to create TSLPR-CART.
Participants will take chemotherapy over 5 days to prepare their body for the therapy; then they will receive the modified cells through a tube inserted into a vein. Staying in the hospital during part of the treatment is expected and participants will be monitored locally to evaluate for side effects. Approximately 1 month after receiving TSLPR-CART, participants will undergo evaluations to see how the TSLPR-CART impacted their leukemia. Participants will have follow-up visits for 2 years after TSLPR-CART either at NIH or at home....
Read the detailed description
Background:
- Philadelphia (Ph)-like acute lymphoblastic leukemia (ALL) is a high-risk subgroup of B-ALL associated with high rates of chemotherapy resistance and relapse. Ph-like ALL is defined by an activated cytokine receptor and kinase signaling profile similar to that of Philadelphia chromosome-positive (Ph+) ALL yet lacking BCR-ABL1 rearrangement.
- Approximately half of childhood and adult Ph-like ALL cases have rearrangement in cytokine receptor like factor-2 (CRLF2), which encodes one subunit of the thymic stromal lymphopoietin receptor (TSLPR) and heterodimerizes with the interleukin-7 receptor alpha (IL7Ra) subunit. Its ligand, TSLP, is a cytokine that plays a critical role in regulation of the immune response and in the differentiation of hematopoietic cells. TSLP binding to the TSLPR in B-ALL induces constitutive Janus kinases and signal transducers and activators of transcription (JAK/STAT) pathway signaling.
- Most CRLF2-rearranged (CRLF2-R) Ph-like ALL cases can be readily identified by increased TSLPR surface expression by flow cytometric immunophenotyping, and specific CRLF2 rearrangements can then be confirmed by genetic testing. Given the prevalence of
CRLF2 rearrangements and the poor clinical outcomes of patients with Ph-like ALL, TSLPR is a promising target for new immunotherapies.
- Chimeric antigen receptor-expressing T cells (CAR) have proven highly successful in patients with cancer with dramatic responses in >70% of patients with relapsed/refractory B-ALL treated with CD19-redirected CAR T cells, resulting in Food and Drug Administration (FDA) approval of a CD19 CAR T-cell immunotherapy in children and young adults. A trial of CAR T cells targeting CD22 is currently ongoing at the NCI and has demonstrated comparable efficacy and toxicity results as the CD19 CAR.
- Emerging data have indicated that not all patients respond, and up to 50% of those who achieve remission will subsequently relapse. The most common cause of relapse is the target antigen loss, which is likely multi-factorial in etiology and for which this mechanism of escape is under active investigation. Novel targets are needed.
- This will be the first in human testing of anti-CRLF2-R/TSLPR CAR T cell (TSLPRCART) adoptive cell therapy.
Objective:
-To assess the safety of administering escalating doses of autologous anti-CRLF2-R/TSLPR-CAR engineered T cells (TSLPR-CART) containing a truncated epidermal growth factor (tEGFR) suicide switch to determine a maximum tolerated dose (MTD) in participants with recurrent or refractory CRLF2/TSLPR-overexpressing B-cell acute lymphoblastic leukemia (ALL) following a cyclophosphamide/fludarabine lymphodepletion regimen.
Eligibility:
- Age >= 18 years
- Participants must have confirmed diagnosis of a B-cell ALL with TSLPR+ expression on flow cytometry who have relapsed or refractory disease after at least one standard chemotherapy regimen and one salvage regimen, with no alternative curative options.
Design:
- This is a first-in-human Phase I trial aimed to determine the safety of TSLPR-CART in participants with recurrent or refractory B-cell ALL.
- Participants will undergo apheresis and TSLPR-CART will be manufactured from the enriched T-cell product
- Participants will receive LD preparative regimen of fludarabine and cyclophosphamide followed by an infusion of TSLPR-CART.
- The MTD of autologous TSLPR-CAR T cells using a 3 + 3 dose escalation design will be determined.
Additional participants in an expansion cohort will be treated at an MTD dose to evaluate the rate of response to TSLPR-CAR T cells. Participants will be evaluated for toxicity, anti-tumor response, CAR expansion and persistence, and other biologic correlatives.
- Conditions
- B-All, Acute Lymphoblastic Leukemia
- Being tested
- TSLPR-CART, Cyclophosphamide, Fludarabine
- Keywords
- Adoptive Immunotherapy, CRLF2-R/TSLPR Expressing Tumor, Acute Lymphoblastic Leukemia, B-All
- Medical subject headings
- Precursor Cell Lymphoblastic Leukemia-Lymphoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TSLPR-CARTBiological
TSLPR CAR transduced T cells on D0 after lymphodepleting preparative regimen
CyclophosphamideDrug
Cyclophosphamide will be diluted in an appropriate solution and infused over one hour. The dose will be based on the patient s body weight, at 500 mg/m^2/dose after fludarabine infusion on days -3 and -2.
FludarabineDrug
Fludarabine is administered as an IV infusion in an appropriate solution over 30 minutes on days -5 through -2. To prevent undue toxicity the dose will be based on BSA (30 mg/m^2/dose).
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | TSLPR-CART at escalating doses Receives: Biological: TSLPR-CART; Drug: Cyclophosphamide; Drug: Fludarabine |
| 2 | Experimental | TSLPR-CART at MTD or highest dose administered Receives: Biological: TSLPR-CART; Drug: Cyclophosphamide; Drug: Fludarabine |
What is being measured
The primary outcome is the main question the study is designed to answer.
To assess the safety of administering escalating doses of TSLPR-CART containing a tEGFR suicide switch to determine an MTD
Safety analyses will consist of tabulations of grades of toxicity by type of toxicity
Measured: 28 days post cell infusion
Secondary outcomes (2)
Efficacy of TSLPR-CART
The Best Overall Response (BOR) will be assessed at end of study, based upon the disease assessments recorded during the study visits, and reported by dose level with a separate evaluation in the 12 participants per category treated at the MTD, in terms of confirmed complete response/partial response (CR/PR), unconfirmed CR/PR, SD, or PD. The rate of relapse from CR prior to end of study will also be summarized by dose level only for the participants who achieve confirmed CR during the study. The overall objective response rate (CR + PR) will be summarized by dose level. The Duration of Response (DOR) will be summarized for those participants who achieve objective response (CR + PR). In participants who have a confirmed response, DOR will be calculated from the first date of documented response until progressive disease (PD). Unconfirmed CR or PR is defined as the first documentation of response
Measured: 2 years post cell infusion
1-year and 2-year OS (overall survival)
OS will be determined as the time from the start of the preparative regimen until death.
Measured: 2 years post cell infusion
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 May 2026
- Study start28 Oct 2026 (estimated)
- Primary completion30 Jun 2030 (estimated)
- Study completion30 Jun 2032 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for B-AllStudies of the same condition, open and under way.
- More trials run by National Cancer Institute (NCI)The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 57 participants (estimated)
Sponsor and investigators
- Lead sponsor
- National Cancer Institute (NCI)
- Sponsor type
- US National Institutes of Health
- Responsible party
- Sponsor
- Investigators
- John W Glod, M.D., Principal investigator, National Cancer Institute (NCI)
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07572136
- Sponsor's protocol ID
- 10001555
- Other IDs
- 001555-C
- Status last verified
- 9 Sep 2026
- First submitted
- 6 May 2026
- Last updated
- 23 Oct 2026
- Results posted
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: This study will comply with the NIH Data Management and Sharing (DMS) Policy, which applies to all new and ongoing NIH-funded research in the IRP, as of January 25, 2023, that is associated with a ZIA, with a clinical protocol that undergoes scientific review and/or will involve genomic data sharing.