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OncoMatch/Clinical Trials/NCT06916767

Phase 1 Study of BAFF CAR-T Cells (LMY-920) for Treatment of Relapsed or Refractory Chronic Lymphocytic Leukemia / Small Lymphocytic Lymphoma

Is NCT06916767 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including BAFF CAR-T and Obinutuzumab for relapsed cll.

Phase 1RecruitingPaolo Caimi, MDNCT06916767Data as of May 2026

Treatment: BAFF CAR-T · Obinutuzumab · Cyclophosphamide · FludarabineCAR-T cell treatment of refractory lymphoma has shown success, particularly with CD-19 targeted CAR-T cells, however, many participants are refractory or relapse after response. Responses are more limited in CLL/SLL, possibly secondary to the suppressive effect of circulating B cells on T cell function. BAFF receptor is a target that has been explored in CLL. Preclinical data indicates that CAR- T cells expressing B-cell activating factor (BAFF) can be another effective strategy to treat refractory CLL. This study aims to explore the efficacy of LMY-920 a BAFF-ligand CAR T cells with depletion of B cells with Obinutuzumab prior to apheresis.

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Extracted eligibility criteria

Cancer type

Chronic Lymphocytic Leukemia

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 2 prior lines

Must have received: BTK inhibitor

Relapsed after 2 or more lines of therapy, including a BTK inhibitor

Must have received: BCL2 inhibitor

Relapsed after 2 or more lines of therapy, including a BCL2 inhibitor

Cannot have received: autologous stem cell transplant

ASCT within 6 weeks of informed consent

Cannot have received: allogeneic hematopoietic stem cell transplantation

History of allogeneic hematopoietic stem cell transplantation

Cannot have received: investigational agent

Less than 28 days elapsed between prior treatment with investigational agent(s) and the day of lymphocyte collection

Lab requirements

Kidney function

calculated creatinine clearance ≥ 30ml/min.

Liver function

total bilirubin ≤ 1.5 x upper institutional limit of normal (except in participants with gilbert's syndrome, active hemolysis or disease involvement of the liver). ast (sgot)/alt ≤ 2.5 x institutional upper limit of normal.

Cardiac function

cardiac ejection fraction of ≥50%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Case Comprehensive Cancer Center, Cleveland Clinic Foundation Taussig Cancer Institute · Cleveland, Ohio

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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