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

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

Status
Active
Cancer Type
Hematopoietic Malignancies
Lymphoma
Non-Hodgkin Lymphoma
Unknown Primary
Trial Phase
Phase III
Eligibility
18 Years and older, Male and Female
Study Type
Treatment
NCT ID
NCT07188558
Protocol IDs
LYL314-102 (primary)
NCI-2026-00303
Study Sponsor
Lyell Immunopharma, Inc.

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.

Objectives

PiNACLE-H2H is a Phase 3 randomized controlled trial comparing the efficacy and safety of
rondecabtagene autoleucel (ronde-cel, formerly known as LYL314) against the currently
approved cluster of differentiation (CD)19 chimeric antigen receptor (CAR) T-cell
therapies (axicabtagene ciloleucel [axi-cel] or lisocabtagene maraleucel [liso-cel]), in
patients with aggressive LBCL that has relapsed or is refractory to first-line anti-CD20
antibody and anthracycline-containing chemotherapy.

Patients will be randomized (1:1) before leukapheresis to receive either:

- Ronde-cel; or

- Investigator's choice of axi-cel or liso-cel

Most patients who receive currently approved CD19-directed CAR T-cell therapies,
including axi-cel and liso-cel, still experience progressive disease, often due to
mechanisms such as CD19 antigen loss or T-cell exhaustion.

Ronde-cel is a novel, autologous, dual-targeting CD19/CD20 CAR T-cell product candidate
enriched for CD62L-positive naïve and central memory T cells, which are associated with
enhanced proliferation capacity and persistence. Ronde-cel is an "OR"-gated CAR construct
that can fully activate upon recognition of either CD19 or CD20, aiming to improve
durability of response despite antigen heterogeneity.

Approximately 400 participants will be enrolled. CAR T-cell therapy in both arms will be
administered as a single intravenous infusion following fludarabine and cyclophosphamide
lymphodepletion. Participants will be followed for 3 years for safety and efficacy, with
long-term follow-up extending to 15 years.

Eligibility

  1. CAR T cell naïve and eligible to receive a CD19 CART-cell therapy
  2. Histologically confirmed large B-cell lymphoma, including the following types defined by (WHO 2022) or International Consensus Classification (2022)
  3. Diffuse large B-cell lymphoma (DLBCL)
  4. Transformations of indolent B-cell lymphomas (excluding Richter's transformation)
  5. DLBCL/High-grade B-cell lymphoma (HGBCL) with MYC and BCL2 rearrangements
  6. High-grade B-cell lymphoma (HGBCL) not otherwise specified (HGBCL NOS)
  7. Primary mediastinal large B-cell lymphoma (PMBCL)
  8. Grade 3B follicular lymphoma/large cell follicular lymphoma (FL3B)
  9. Relapsed or refractory disease after anti-CD20 antibody and anthracycline-containing first-line chemoimmunotherapy
  10. Measurable disease by presence of [18F]-fluorodeoxyglucose PET/CT positive lesion during Screening per Lugano Criteria
  11. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  12. Adequate hematological, renal, hepatic, pulmonary, and cardiac function Key

Treatment Sites in Georgia

Northside Hospital Cancer Institute


1000 Johnson Ferry Road NE
Atlanta, GA 30342
404-303-3355
www.northside.com

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