Recruiting
Phase 1

BAFFR CAR-T with Fludarabine & Cyclophosphamide

Sponsor:

Mayo Clinic

Code:

NCT06191887

Conditions

B-Cell Non-Hodgkin Lymphoma

Recurrent Chronic Lymphocytic Leukemia

Recurrent Diffuse Large B-Cell Lymphoma

Recurrent Follicular Lymphoma

Recurrent Mantle Cell Lymphoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Autologous BAFFR-targeting CAR T Cells

Bendamustine

Biopsy

Biospecimen Collection

Bone Marrow Aspiration and Biopsy

Study Details

Brief summary:

This phase I trial tests safety, side effects and best dose of B-cell activating factor receptor (BAFFR)-based chimeric antigen receptor T-cells, with fludarabine and cyclophosphamide lymphodepletion, for the treatment of patients with B-cell hematologic malignancies that has come back after a period of improvement (relapsed) or that does not respond to treatment (refractory). BAFFR-based chimeric antigen receptor T-cells is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so they will attack cancer cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's cancer cells is added to the T cells in the laboratory. The special receptor is called a chimeric antigen receptor (CAR). Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain cancers. Giving chemotherapy, such as fludarabine and cyclophosphamide, helps ill cancer cells in the body and helps prepare the body to receive the BAFFR based chimeric antigen receptor T-cells. Giving BAFFR based chimeric antigen receptor T-cells with fludarabine and cyclophosphamide for lymphodepletion may work better for the treatment of patients with relapsed or refractory B-cell hematologic malignancies.

Conditions

B-Cell Non-Hodgkin Lymphoma

Recurrent Chronic Lymphocytic Leukemia

Recurrent Diffuse Large B-Cell Lymphoma

Recurrent Follicular Lymphoma

Recurrent Mantle Cell Lymphoma

Study ID

NCT06191887

Start date

Mar 18, 2024

Status verified date

Feb, 2026

Completion date

Dec 31, 2040

Anticipated

Primary completion date

Dec 31, 2040

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • PRE-REGISTRATION: Age ≥ 18 years
  • PRE-REGISTRATION: Confirmed diagnosis of 1 of the following relapsed or refractory B-cell hematologic malignancies: chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), follicular lymphoma (FL), mantle cell lymphoma (MCL), marginal zone lymphoma (MZL), or large B cell lymphoma (LBCL) including Richter's transformation from CLL/SLL

  • For CD19+ B cell malignancies; relapsed or refractory disease is defined by one of the following histopathology:

  • Biopsy proven SLL or flow cytometry proven CLL; relapsed or refractory disease is defined as:
  • Demonstration of progressive or stable disease by positron emission tomography/computed tomography (PET/CT) or computed tomography (CT) criteria according to the international workshop on chronic lymphocytic leukemia (iwCLL) 2018 criteria
  • Biopsy proven B-cell non-Hodgkin lymphoma (NHL) of any histopathology (including Richter Transformation of CLL); relapsed or refractory disease is defined as:
  • Demonstration of progressive or stable disease by PET/CT or CT criteria as the best response to the most recent chemotherapy regimen according to the revised Lugano Response Criteria for Malignant Lymphoma
  • PRE-REGISTRATION: Disease Specific prior lines of therapies below:

  • For CLL/SLL, patients must have received ≥ two prior lines of therapy, and/or ≥ 6 months of second line prior BTK inhibition (e.g. ibrutinib or other such as acalabrutinib or zanubrutinib) and must have failed to respond to venetoclax or be intolerant. Exception: Patients in stable disease (SD) or partial response (PR) with a known ibrutinib resistance mutation (BTK or phospholipase Cγ2) may be included even if on ibrutinib therapy for less than 6 months

  • These patients may or may not have received prior antibody directed against cluster of differentiation 20 (CD20).
  • For Follicular Lymphoma, patients must have received ≥ two prior lines of therapy, including an antibody directed against CD20.

  • NOTE: Prior cluster of differentiation 19 (CD19) directed chimeric antigen receptor T-cell therapy (CART) must have a 100-day washout period.
  • For Mantle Cell Lymphoma, patients must have received ≥ two prior lines of therapy, including an antibody directed against CD20, and a BTK inhibitor.

  • NOTE: Prior CD19 directed CART must have a 100-day washout period.
  • For Marginal Zone Lymphoma, patients must have received ≥ two prior lines of therapy, including an antibody directed against CD20.

  • NOTE: Prior CD19 directed CART must have a 100-day washout period.
  • For Large B cell Lymphoma, patients must have received ≥ two prior lines of therapy, including an antibody directed against CD20. Prior exposure to CD19 directed CART will be allowed at the discretion of the Principal Investigator.

  • NOTE: Prior failed CD19 directed CART must have a 100-day washout period
  • For Richter's Transformation, patients must have received ≥two prior lines of therapy, including an antibody directed against CD20.
  • 100-day washout period starts from the date of the last prior CAR-T infusion.
  • PRE-REGISTRATION: Measurable disease
  • REGISTRATION: Positive BAFFR test
  • REGISTRATION: Measurable disease
  • REGISTRATION: Eastern Cooperative Oncology Group (ECOG) performance status 0, 1 or 2
  • REGISTRATION: Hemoglobin ≥ 9.0 g/dL (unless due to documented marrow involvement with disease) obtained ≤14 days prior to registration
  • REGISTRATION: Absolute neutrophil count (ANC) ≥ 1500/mm\^3 (unless due to documented marrow involvement with disease) obtained ≤14 days prior to registration
  • REGISTRATION: Platelet count ≥100,000/mm\^3 (unless due to documented marrow involvement with disease) obtained ≤ 14 days prior to registration
  • REGISTRATION: Total bilirubin ≤ 1.5 x upper limits of normal (ULN) (Subjects with Gilbert's Syndrome may be included if their total bilirubin is ≤ 3.0 x ULN and direct bilirubin ≤ 1.5 x ULN) obtained ≤ 14 days prior to registration
  • REGISTRATION: Alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 3 x ULN (≤ 5 x ULN for patients with liver involvement) obtained ≤ 14 days prior to registration
  • REGISTRATION: Prothrombin time (PT)/international normalized ratio (INR) /activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN OR if patient is receiving anticoagulant therapy and INR or aPTT is within target range of therapy obtained ≤ 14 days prior to registration

  • Patients on a stable, maintenance regimen of anticoagulant therapy for ≥ 30 days prior to registration may have PT/INR measurements > 1.5 X ULN if, in the judgment of the investigator, the patient is suitable for the study
  • REGISTRATION: Calculated creatinine clearance ≥45 ml/min using the Cockcroft-Gault formula obtained ≤ 14 days prior to registration
  • REGISTRATION: Negative pregnancy test done ≤ 7 days prior to registration, for persons of childbearing potential only. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • REGISTRATION: Provide written informed consent understand and comply with protocol-required study procedures
  • REGISTARTION: Patients must have an ejection fraction (EF) of ≥ 45%
  • REGISTRATION: Patients must have pulse ox measurements of > 92% on room air
  • REGISTRATION: Willingness to provide mandatory blood specimens for correlative research
  • REGISTRATION: Willing to return to enrolling institution for study follow-up

Exclusion Criteria:

  • PRE-REGISTRATION: Prior solid organ transplantation
  • PRE-REGISTRATION: Unstable angina, clinically significant arrhythmia, or myocardial infarction ≤ 6 months of prior to pre-registration, or grade 3 or higher pericardial effusion at the time of pre-registration
  • PRE-REGISTRATION: Prior anti-BAFF-R therapies
  • PRE-REGISTRATION: Known contraindication to lymphodepleting (LD) chemotherapy
  • PRE-REGISTRATION: Use of systemic antitumor therapy or investigational agent ≤ 14 days, prior to pre-registration
  • PRE-REGISTRATION: Receiving any other investigational agent which would be considered as a treatment for the BAFF-R
  • PRE-REGISTRATION: Autologous HCT ≤ 60 days prior to pre-registration
  • PRE-REGISTRATION: Uncontrolled intercurrent non-cardiac illness including, but not limited to:

  • Previous or concurrent malignancy
  • Ongoing or active infection
  • Psychiatric illness/social situations
  • Dyspnea at rest due to complications of advanced malignancy or other disease that requires continuous oxygen therapy \* Persons of childbearing potential who are pregnant or breastfeeding
  • Life Expectancy of < 6 weeks
  • Persons requiring systemic corticosteroids (>10 mg prednisone or equivalent per day) and/or other immunosuppressive therapy. Patients are allowed to use topical corticosteroids
  • Any other conditions that would limit compliance with study requirements
  • PRE-REGISTRATION: Detectable malignant cells from cerebrospinal fluid (CSF) or magnetic resonance imaging (MRI) indicating brain metastases during screening, or a history of central nervous system (CNS) involvement by malignancy (CSF or imaging) with still active disease. Note: Patients with a history of CNS involvement resolving after treatment and without active disease will be considered eligible if other inclusion criteria are met
  • PRE-REGISTRATION: History of a seizure disorder, major cerebrovascular ischemia/hemorrhage, dementia, cerebellar disease, or any autoimmune disease with CNS involvement
  • PRE-REGISTRATION: Radiation therapy ≤ 14 days prior to pre-registration
  • PRE-REGISTRATION: Prior allogeneic hematopoietic stem cell transplant (HCT) in ≤ 6 months prior to pre-registration; patients with active graft versus host disease (GVHD) will not be eligible regardless of duration from prior allogeneic HCT
  • PRE-REGISTRATION: Human immunodeficiency virus (HIV) positive patients
  • PRE-REGISTRATION: Subjects with New York Health Association (NYHA) class III or greater heart failure
  • REGISTRATION: Eligible for auto-HCT based on investigator judgement
  • REGISTRATION: Presence of active bacterial, viral, or fungal infection that is uncontrolled, based on investigator judgment
  • REGISTRATION: Patients with active hepatitis B or hepatitis C infections are excluded from the study. Patients who are documented to be HIV positive or proven HIV infection from testing are ineligible for the study. Infectious disease testing (HIV-1, HIV-2, hepatitis C virus (HCV) antibody and polymerase chain reaction (PCR), hepatitis B virus (HBV) surface antigen, HBV surface antibody, HBV core antibody) performed ≤ 45 days prior to registration may be considered for subject eligibility
  • REGISTRATION: Previous or concurrent malignancy, except basal cell or squamous cell skin carcinoma, adequately resected and in situ carcinoma of cervix, or a previous malignancy that was completely resected and has been in remission for ≥ 5 years prior to registration
  • REGISTRATION: Persons of childbearing potential who are pregnant or breastfeeding
  • REGISTRATION: Life expectancy of < 6 weeks

Study Design

Enrollment

27 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Treatment (BARRF based chimeric antigen receptor T-cells)

Patients undergo leukapheresis. Patients then receive cyclophosphamide IV, over 60 minutes and fludarabine IV over 30 minutes on day -5 to -3 or bendamustine IV over 10 minutes on days -4 and -3. Patients receive BAFFR based chimeric antigen receptor T-cells IV on day 0. Patients undergo echocardiography and MRI at screening, CT scan, PET scan, bone marrow biopsy/aspirate and blood sample collection throughout the study and tumor biopsy at progression.

Interventions

Autologous BAFFR-targeting CAR T Cells

Given IV

Bendamustine

Given IV

Biopsy

Undergo biopsy

Biospecimen Collection

Undergo blood sample collection

Bone Marrow Aspiration and Biopsy

Undergo bone marrow biopsy/aspirate

Computed Tomography

Undergo CT scan

Cyclophosphamide

Given IV

Echocardiography

Undergo echocardiography

Fludarabine

Given IV

Leukapheresis

Undergo leukapheresis

Magnetic Resonance Imaging

Undergo MRI

Positron Emission Tomography

Undergo PET scan

Primary outcome measure

  • Incidence of dose-limiting toxicities (DLT) [ Time Frame: Up to 28 days after MC10029 (autologous B-cell activating factor receptor [BAFFR]-targeting chimeric antigen receptor [CAR] T cells product) infusion ]
  • Incidence and severity of treatment emergent adverse events [ Time Frame: Up to 15 years ]

Central Contacts and Locations

Locations

Mayo Clinic in Florida

Recruiting

Jacksonville, Florida, United States, 32224-9980

Contacts

Clinical Trials Referral Office

855-776-0015mayocliniccancerstudies@mayo.edu

Principal Investigator:

Mohamed A. Kharfan-Dabaja, M.D., M.B.A.

More Information

Sponsor

Mayo Clinic

Last update posted

Feb 13, 2026

Last verified

Feb, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Mayo Clinic on 2026-02-13.