About this trial

This Phase 3 study compares rondecabtagene autoleucel (ronde-cel), a dual-targeting CD19/CD20 CAR T-cell therapy, with investigator's choice of CD19 CAR T-cell therapy in patients with relapsed or refractory large B-cell lymphoma in the second-line setting.

Eligibility criteria

Qualifiers

CAR T cell naïve and eligible to receive a CD19 CART-cell therapy

Histologically confirmed large B-cell lymphoma, including the following types defined by (WHO 2022) or International Consensus Classification (2022)

Diffuse large B-cell lymphoma (DLBCL)

Transformations of indolent B-cell lymphomas (excluding Richter's transformation)

Disqualifiers

Patients ineligible to receive CD19 CAR T-cell therapy

Primary CNS lymphoma

Patients with primary cutaneous LBCL, human herpes virus-8 positive lymphoma, Burkitt lymphoma, T cell histiocyte-rich lymphoma, or transformation from chronic lymphocytic leukemia/small lymphocytic lymphoma (Richter's transformation)

Patients with prior history of malignancy, other than aggressive relapsed or refractory LBCL, unless the patient has been free of the disease for ≥ 2 years

Trial design

Treatments tested in this trial

  • rondecabtagene autoleucel
  • axicabtagene ciloleucel
  • lisocabtagene maraleucel

Treatment groups

400 Participants
are divided into 2 treatment groups

Locations

38
Arizona
Banner MD Anderson Cancer Center85234, Gilbert United States
Honor Health85258, Scottsdale United States
Mayo Clinic Arizona85259, Scottsdale United States
Arkansas
University of Arkansas72205, Little Rock United States

Sponsors and collaborators

Lyell Immunopharma, Inc.

Lead sponsor