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临床试验/NCT07188558
NCT07188558招募中3 期

A Phase 3 Randomized Controlled Trial of Rondecabtagene Autoleucel , an Autologous, Dual-targeting CD19/CD20 CAR T-Cell Product Candidate, Vs. Investigator's Choice of CD19 CAR T-Cell Therapy in Patients With Relapsed or Refractory Large B-Cell Lymphoma in the Second-line Setting

Lyell Immunopharma, Inc.63 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2026年1月12日最近更新:
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
400
试验地点
63
主要终点
Event free survival

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Rondecabtagene autoleucel

Experimental

干预措施: rondecabtagene autoleucel (Biological)

Investigator's Choice CD19

Active Comparator

axicabtagene ciloleucel, lisocabtagene maraleucel

干预措施: lisocabtagene maraleucel (Biological)

Investigator's Choice CD19

Active Comparator

axicabtagene ciloleucel, lisocabtagene maraleucel

干预措施: axicabtagene ciloleucel (Biological)

结局指标

主要结局

Event free survival

时间窗: 36 months

The time interval from treatment initiation until the occurrence of a specific event of interest.

次要结局

  • Overall Response Rate(36 months)
  • Complete Response Rate(36 months)
  • Progression Free Survial(36 months)
  • Overall Survival(6 years)
  • Incidence and severity adverse events(36 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (63)

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