NCT05784441进行中（未招募）1 期
A Phase 1b Multicenter, Open-Label, Study of JNJ-90009530, an Autologous Anti-CD20 CAR-T Cell Therapy in Adult Participants With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 21
- 试验地点
- 15
- 主要终点
- Calculate the Occurence of Adverse Events
研究概览
简要总结
The goal of this multicenter study is to test JNJ-90009530 in Relapsed or Refractory Non-Hodgkin Lymphoma Patients. The main questions the study aims to answer are:
- can a dose of JNJ-90009530 be determined that is safe and well tolerated by patients.
- will JNJ-90009530 help patients achieve a response and for how long?
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 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
- •Participant must be greater than or equal to (>=) 18 years of age, at the time of signing informed consent
- •All participants must have relapsed or refractory disease for each histologic subtype
- •Mature aggressive large B cell NHL and Follicular Lymphoma Grade 3b: Participants must have >= 2 lines of systemic therapy or >=1 line of systemic therapy in case of participants ineligible for high-dose chemotherapy and autologous Hematopoietic stem cell transplantation (HSCT). Participants also must have had exposure to an anthracycline and an anti-CD20 targeted agent
- •Follicular lymphoma Grade 1-3a and Marginal Zone Lymphoma: Participants must have >=2 prior lines of anti-neoplastic systemic therapy. Participants also must have prior exposure to an anti-CD20 monoclonal antibody
- •Tumor must be cluster of differentiation (CD) 20 positive
- •Measurable disease as defined by Lugano 2014 classification
- •Eastern Cooperative Oncology Group (ECOG) performance status of either 0 or 1
排除标准
- •Diagnosis of Human herpes virus (HHV) 8-positive Diffuse large B Cell lymphoma (DLBCL)
- •Prior allogeneic Hematopoietic stem cell transplantation (HSCT)
- •Autologous stem cell transplant within 12 weeks of chimeric antigen receptor (CAR) T cell infusion
- •Uncontrolled active infections
- •History of deep vein thrombosis or pulmonary embolism within six months of infusion (except for line associated deep vein thrombosis [DVT])
- •History of stroke, unstable angina, myocardial infarction, congestive heart failure ( New York Heart Association [NYHA] Class III or IV), severe cardiomyopathy or ventricular arrhythmia requiring medication or mechanical control within 6 months of screening
- •History of a seizure disorder, dementia, cerebellar disease or neurodegenerative disorder
- •Known history or prior diagnosis of optic neuritis or other immunologic or inflammatory disease affecting the central nervous system
- •Active central nervous system (CNS) involvement by malignancy
- •Current active liver or biliary disease (except for Gilbert's syndrome or asymptomatic gallstones)
研究组 & 干预措施
JNJ-90009530
Experimental
干预措施: JNJ-90009530 (Drug)
结局指标
主要结局
Calculate the Occurence of Adverse Events
时间窗: up to 24 months
The safety and tolerability will be measured by recording the occurence and severity of all adverse events or dose limiting toxicities that occur according to Common Terminology Criteria for Adverse Events (CTCAE) criteria version 5.0
Determine Recommended Phase 2 dose (RP2D)
时间窗: up to 24 months
Employ a Bayesian optimal interval (BOIN) design and determine the RP2D with review of the number of dose-limiting toxicities
次要结局
- Determine the Overall Response (OR)(up to 24 months)
- Determine the time to response (TTR)(up to 24 months)
- Determine the duration of response (DOR)(up to 24 months)
- Measure the amount of JNJ-90009530 in blood over time(up to 24 months)
研究者
研究点 (15)
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