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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2400086700 |
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最近更新日期: Date of Last Refreshed on: |
2024-07-09 10:32:13 |
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注册时间: Date of Registration: |
2024-07-09 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
评价阿基仑赛注射液治疗一线免疫化疗无效或在一线免疫化疗后12个月内复发的成人大B细胞淋巴瘤(r/r LBCL)的非干预性临床研究 |
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Public title: |
A non-interference clinical study to evaluate the treatment of adult large B-cell lymphoma (r/r LBCL) with Axicabtagene Ciloleucel Injection that is refractory to first-line chemoimmunotherapy or relapses within 12 months of first-line chemoimmunotherapy. |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
评价阿基仑赛注射液治疗一线免疫化疗无效或在一线免疫化疗后12个月内复发的成人大B细胞淋巴瘤(r/r LBCL)的非干预性临床研究 |
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Scientific title: |
A non-interference clinical study to evaluate the treatment of adult large B-cell lymphoma (r/r LBCL) with Axicabtagene Ciloleucel Injection that is refractory to first-line chemoimmunotherapy or relapses within 12 months of first-line chemoimmunotherapy. |
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研究课题代号(代码): Study subject ID: |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
杨兵 |
研究负责人: |
赵维莅 |
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Applicant: |
Bing Yang |
Study leader: |
Weili Zhao |
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申请注册联系人电话: Applicant telephone: |
+86 186 2165 2633 |
研究负责人电话: Study leader's telephone: |
+86 21 6437 0045 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
bing.yang@fosunkitebio.com |
研究负责人电子邮件: Study leader's E-mail: |
zhao.weili@yahoo.com |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
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申请注册联系人通讯地址: |
上海市闵行区合川路2570号1号楼1101室 |
研究负责人通讯地址: |
中国上海市黄浦区瑞金二路197号 |
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Applicant address: |
Room 1101, Building 1, No. 2570 Hechuan Road, Minhang District, Shanghai, China |
Study leader's address: |
197 Second Ruijin Road, Huangpu District, Shanghai, China |
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申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
复星凯特生物科技有限公司 |
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Applicant's institution: |
Fosun Kite Biotechnology Co., Ltd |
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研究负责人所在单位: |
上海市交通大学医学院附属瑞金医院 |
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Affiliation of the Leader: |
Ruijin Hospital, School of Medicine, Shanghai Jiaotong University |
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是否获伦理委员会批准: |
是/Yes |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
(2024)伦审第(1)号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
上海交通大学医学院附属瑞金医院药物临床试验伦理委员会 |
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Name of the ethic committee: |
Ruijin Hospital Ehics Committee, Shanghai JiaoTong University School of Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-01-05 00:00:00 |
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伦理委员会联系人: |
刘海莉 |
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Contact Name of the ethic committee: |
Haili Liu |
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伦理委员会联系地址: |
上海市瑞金二路197号 |
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Contact Address of the ethic committee: |
197 Second Ruijin Road, Huangpu District, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 3418 8900 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
iec2020@rjh.com.cn |
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研究实施负责(组长)单位: |
上海市交通大学医学院附属瑞金医院 |
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Primary sponsor: |
Ruijin Hospital, School of Medicine, Shanghai Jiaotong University |
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研究实施负责(组长)单位地址: |
中国上海市黄浦区瑞金二路197号 |
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Primary sponsor's address: |
197 Second Ruijin Road, Huangpu District, Shanghai, China |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
复星凯特生物科技有限公司 |
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Source(s) of funding: |
Fosun Kite Biotechnology Co., Ltd |
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Target disease: |
large B cell lymphoma |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
评价上市后阿基仑赛注射液治疗一线免疫化疗无效或在一线免疫化疗后12 个月内复发的成人大B 细胞淋巴瘤(r/r LBCL)的疗效和安全性,并建立中国r/r LBCL 成人受试者接受阿基仑赛注射液治疗的真实世界数据。 |
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Objectives of Study: |
Evaluate the efficacy and safety of Axicabtagene Ciloleucel Injection in treatment of adult large B-cell lymphoma (r/r LBCL) with refractory first-line chemoimmunotherapy or relapses within 12 months of first-line chemoimmunotherapy, and establish real world data on Chinese r/r LBCL adult subjects receiving Axicabtagene Ciloleucel Injection treatment. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
1.在中国获得复星凯特商业认证的研究中心中接受复星凯特免疫细胞治疗产品——阿基仑赛注射液治疗一线免疫化疗无效或在一线免疫化疗后12 个月内复发的大B 细胞淋巴瘤(r/rLBCL)成人受试者。2. 患者诊断为大B 细胞淋巴瘤,亚型包括DLBCL NOS(通过排除独特特征定义并根据起源细胞类型进一步分为生发中心B 细胞[GCB] 和活化B 细胞[ABC])和其他具有独特临床和病理学特征的不同DLBCL 实体如原发性皮肤DLBCL,腿型;EB 病毒阳性(EBV)+ DLBCL NOS;EBV+ 皮肤黏膜溃疡;慢性炎症相关性DLBCL;以及富含T 细胞/组织细胞的LBCL。LBCL 还包括滤泡性淋巴瘤(FL)转化的DLBCL。但本研究不包括原发性中枢神经系统淋巴瘤(PCNSL)。3. 所有参加本研究的患者必须签署知情同意书,对于不具有完全民事行为能力的患者,其监护人必须获得知情并签署相应的知情同意书并注明日期。 |
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Inclusion criteria |
1.Participate in the trial conducted at the Fosun Kite commercial authorization investigational sites in China, receiving Fosun Kite's immunocellular therapy product——Axicabtagene Ciloleucel Injection, for adult patients with large B-cell lymphoma (LBCL) that is refractory to first-line chemoimmunotherapy or relapses within 12 months of first-line chemoimmunotherapy. 2.Histologically proven large B-cell lymphoma including the following types DLBCL not otherwise specified (ABC/GCB) Primary cutaneous DLBCL, leg type Epstein-Barr virus (EBV) + DLBCL Epstein-Barr virus (EBV) + mucocutaneous ulcer DLBCL associated with chronic inflammation T-cell/histiocyte rich large B-cell lymphoma DLBCL arising from FL This study does not include primary central nervous system lymphoma (PCNSL). 3. All patients participating in this study must sign an informed consent form. For patients who do not have full capacity for civil conduct, their guardians must sign and date the informed consent form after obtaining informed consent. |
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排除标准: |
1. 患者为二线或者二线以上治疗后复发。 2. 初治大B 细胞淋巴瘤患者。 |
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Exclusion criteria: |
1. The patients relapses after second-line or above treatment. 2. The patients with newly treated large B-cell lymphoma. |
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研究实施时间: Study execute time: |
从 From 2023-12-01 00:00:00至 To 2030-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-07-15 00:00:00 至 To 2026-06-30 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
无 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
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盲法: |
开放标签 |
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Blinding: |
Open Label |
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是否共享原始数据: IPD sharing |
No |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
不适用 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not Applicable |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |