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
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
- 否
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
干预措施: rondecabtagene autoleucel (Biological)
Investigator's Choice CD19
axicabtagene ciloleucel, lisocabtagene maraleucel
干预措施: lisocabtagene maraleucel (Biological)
Investigator's Choice CD19
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)
