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A Study to Investigate Ronde-cel Versus Investigator's Choice CD19 CAR T-Cell Therapy

About

Brief Summary

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.

Primary Purpose
The main objective of the intervention(s) being evaluated by the clinical trial. Learn more
Treatment
Study Type
The nature of the investigation or investigational use for which clinical study information is being submitted. Learn more
Interventional
Phase
Phase 3

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
N/A

Key Inclusion Criteria:

  • 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)
    • DLBCL/High-grade B-cell lymphoma (HGBCL) with MYC and BCL2 rearrangements
    • High-grade B-cell lymphoma (HGBCL) not otherwise specified (HGBCL NOS)
    • Primary mediastinal large B-cell lymphoma (PMBCL)
    • Grade 3B follicular lymphoma/large cell follicular lymphoma (FL3B)
  • Relapsed or refractory disease after anti-CD20 antibody and anthracycline-containing first-line chemoimmunotherapy
  • Measurable disease by presence of [18F]-fluorodeoxyglucose PET/CT positive lesion during Screening per Lugano Criteria
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Adequate hematological, renal, hepatic, pulmonary, and cardiac function

Key Exclusion Criteria:

  • 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
  • Patients with uncontrolled systemic fungal, bacterial, viral, or other infection (including tuberculosis) despite appropriate antibiotics or other treatment
  • Active autoimmune disease requiring ongoing systemic immunosuppressive therapy.

Note: Other protocol defined Inclusion/Exclusion criteria may apply

Study Stats
Protocol No.
25-2645
Category
Lymphoma
Principal Investigator
Sarah M. Larson, MD
Sarah M. Larson, MD
Hematologic Malignancy
Sarah M. Larson, MD
Contact
  • Lisa Del Rio
  • Rodrigo Marin
Location
  • UCLA Westwood
For Providers
NCT No.
NCT07188558
For detailed technical eligibility, visit ClinicalTrials.gov.