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OncoMatch/Clinical Trials/NCT05826535

Study of LYL314 in Aggressive Large B-Cell Lymphoma

Is NCT05826535 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies multiple treatments including LYL314 and Fludarabine for relapsed non-hodgkin lymphoma.

Phase 1/2RecruitingLyell Immunopharma, Inc.NCT05826535Data as of May 2026

Treatment: LYL314 · Fludarabine · CyclophosphamideThis is a Phase 1/2, multi-center, open-label study evaluating the safety and efficacy of LYL314, a dual-targeting chimeric antigen receptor (CAR) targeting cluster of differentiation (CD)19 and CD20 in participants with aggressive large B-cell lymphoma.

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Extracted eligibility criteria

Cancer type

Non-Hodgkin Lymphoma

Diffuse Large B-Cell Lymphoma

Performance status

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

Prior therapy

Min 2 prior lines

Must have received: anti-CD20 monoclonal antibody

Prior therapy must have included: Anti-CD20 monoclonal antibody

Must have received: anthracycline

Prior therapy must have included: An anthracycline containing chemotherapy regimen

Cannot have received: allogeneic stem cell transplantation

History of allogeneic stem cell or solid organ transplantation

Cannot have received: autologous stem cell transplantation

Exception: within 6 weeks prior to enrollment/leukapheresis

Receipt of autologous stem cell transplantation within 6 weeks prior to enrollment/leukapheresis

Cannot have received: genetically modified cell therapy

Exception: CD19 with an FMC63-based CAR (e.g., axi-cel, tisa-cel, liso-cel) allowed

History of prior genetically modified cell therapy other than a product targeting CD19 with an FMC63-based CAR (e.g., axicabtagene ciloleucel (axi-cel), tisagenlecleucel (tisa-cel), or lisocabtagene maraleucel (liso-cel). For all other CAR T cell therapy treatments, discussion with the Sponsor's Medical Monitor is required

Lab requirements

Blood counts

ANC ≥ 1000/uL; Platelet count ≥ 50,000/uL; Absolute lymphocyte count (ALC) ≥ 200/uL

Absolute neutrophil count (ANC) ≥ 1000/uL; Platelet count ≥ 50,000/uL; Absolute lymphocyte count (ALC) ≥ 200/uL

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

US trial sites

  • University of California-Irvine Medical Center · Irvine, California
  • Cedars-Sinai Medical Center · Los Angeles, California
  • University of California, Los Angeles (UCLA) Medical Center · Los Angeles, California
  • Scripps Clinic · San Diego, California
  • Colorado Blood Cancer Institute · Denver, Colorado

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

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