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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: |
ChiCTR2400087275 |
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最近更新日期: Date of Last Refreshed on: |
2024-07-24 12:03:21 |
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注册时间: Date of Registration: |
2024-07-24 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
瑞帕妥单抗单药或联合其他药物治疗B细胞非霍奇金淋巴瘤的疗效及安全性 |
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Public title: |
Efficacy and Safety of Ripertamab With or Without Other Drugs in B-cell Non-Hodgkin's Lymphomas |
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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: |
瑞帕妥单抗治疗 B 细胞非霍奇金淋巴瘤患者的疗效及安全性真实世界研究 |
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Scientific title: |
The Efficacy and Safety of Ripertamab in B-cell Non-Hodgkin Lymphomas: a Real-world Study |
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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: |
张金艳 |
研究负责人: |
马军 |
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Applicant: |
zhang jinyan |
Study leader: |
ma jun |
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申请注册联系人电话: Applicant telephone: |
+86 185 1140 5431 |
研究负责人电话:
Study leader's |
+86 133 0451 8000 |
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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: |
jinyan_zhang@sinocelltech.com |
研究负责人电子邮件: Study leader's E-mail: |
majun0322@126.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: |
北京市经济技术开发区科创七街31号 |
研究负责人通讯地址: |
哈尔滨市道里区地段街149号 |
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Applicant address: |
31 Kechuang Seventh Street, Economic and Technological Development Zone, Beijing |
Study leader's address: |
149 diduan street,Daoli District, Harbin |
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申请注册联系人邮政编码: Applicant postcode: |
394656 |
研究负责人邮政编码: Study leader's postcode: |
394656 |
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申请人所在单位: |
神州细胞工程有限公司 |
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Applicant's institution: |
Shenzhou Cell Engineering Co., Ltd. |
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研究负责人所在单位: |
哈尔滨市第一医院血液肿瘤研究中心 |
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Affiliation of the Leader: |
Institute of Hematology and Oncology, Harbin The First Hospital |
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是否获伦理委员会批准: |
是 |
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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: |
IIT-2023-002 |
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: |
哈尔滨市第一医院血液肿瘤研究中心 |
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Name of the ethic committee: |
Institute of Hematology and Oncology, Harbin The First Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-05-25 00:00:00 | ||
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伦理委员会联系人: |
程梅 |
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Contact Name of the ethic committee: |
cheng mei |
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伦理委员会联系地址: |
哈尔滨市道里区地段街149号 |
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Contact Address of the ethic committee: |
149 diduan street,Daoli District, Harbin |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 136 1366 5821 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
哈尔滨市第一医院 |
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Primary sponsor: |
Institute of Hematology and Oncology, Harbin The First Hospital |
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研究实施负责(组长)单位地址: |
哈尔滨市道里区地段街149号 |
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Primary sponsor's address: |
149 diduan street,Daoli District, Harbin |
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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: |
自筹 |
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Source(s) of funding: |
self-raised |
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研究疾病: |
淋巴瘤 |
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Target disease: |
Lymphomas |
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研究疾病代码: |
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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: |
描述B细胞非霍奇金淋巴瘤患者的治疗现状,评估雷帕妥珠单抗在现实世界中B细胞非霍奇金淋巴瘤患者的疗效和安全性。 |
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Objectives of Study: |
To describe the current state of treatment for patients with B-cell non-Hodgkin's lymphoma and to assess the efficacy and safety of Ripertamab in real-world patients with B-cell non-Hodgkin's lymphoma |
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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)年龄:≥18岁; (2)经病理组织学证实的CD20阳性的B细胞非霍奇金淋巴瘤患者,符合下列任一标准:a)既往未经过治疗;b)既往接受过最多不超过二线治疗,包括化疗、免疫治疗、针对淋巴瘤的局部放疗等; (3)ECOG 体力状态评分为 0-2; (4)预计生存期≥6 个月; (5)肝肾功能正常者,具体为血清直接胆红素、血清间接胆红素和/或谷丙转氨酶、谷草转氨酶、血清肌酐≤2×正常值上限(ULN),肌酐清除率≥60 mL/min; (6)患者具有充分的血液学功能,无论骨髓受侵与否均需符合以下指标: 绝对中性粒细胞计数≥1.0×109/L、血小板计数≥50×109/L; (7)对于未接受绝育手术的育龄期男性或女性,需同意在治疗期间和瑞帕妥单抗末次给药后6 个月内进行避孕; (8)受试者自愿加入本研究,并签署知情同意书,依从性好,配合随访。 (9)研究者评估接受瑞帕妥单抗治疗可以获益的患者; |
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Inclusion criteria |
(1) Age: ≥18 years; (2) Patients with pathologically histologically confirmed CD20-positive B-cell non-Hodgkin's lymphoma ,meeting any of the following criteria: a) previously untreated; b) having received up to second-line therapy, including chemotherapy, immunotherapy, and local radiotherapy for lymphoma; (3) ECOG score is 0-2; (4) More than 6 months life expectancy ; (5) Normal liver and kidney function, specifically serum direct bilirubin, serum indirect bilirubin and/or glutathione aminotransferase, glutamic oxalacetic aminotransferase, serum creatinine ≤ 2 x upper limit of normal (ULN), and creatinine clearance ≥ 60 mL/min; (6) Patients with adequate hematologic function, regardless of bone marrow invasion or not, must meet the following indicators: absolute neutrophil count ≥ 1.0 × 109/L and platelet count ≥ 50 × 109/L; (7) For men or women of childbearing age who have not undergone sterilization, consent for contraception during treatment and for 6 months after the last dose of Ripertamab is required; (8) Subjects voluntarily enrolled in this study and signed an informed consent form with good compliance and cooperation with follow-up. (9) Patients who can benefit from treatment with repatumumab are evaluated by the investigator. |
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排除标准: |
(1)对治疗方案中的任何药物有禁忌症; (2)妊娠或哺乳期妇女; (3)疾病累及中枢神经系统者; (4)既往患有其它恶性肿瘤(已治愈的皮肤基底细胞癌或皮肤鳞状细胞癌,或皮肤黑色素瘤或宫颈原位癌除外); (5)合并有可能影响研究方案依从性的显著控制不佳的疾病,例如严重心血管疾病、周围神经系统或中枢神经系统疾病; (6)HCV抗体阳性且HCV-RNA 定性检测≥104 拷贝/mL;或HBV检查结果为:HBsAg 阳性和/或 HBcAb 阳性且 HBV DNA 滴度高于1000 IU/mL或者1000 拷贝/mL者; (7)有未控制的心脏病,包括不稳定性心绞痛、第一次服用药物前6个月内有急性心肌梗死、充血性心力衰竭(NYHA)心功能分级于III级或IV级;或心脏左室射血分数<50%; (8)有免疫缺陷病史,包括 HIV 阳性或患有其它获得性、先天性免疫缺陷疾病或有器官移植史者; (9)研究者认为不适合入组的患者。 |
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Exclusion criteria: |
(1) Contraindication to any drug in the treatment regimen; (2) Pregnant or lactating women; (3) Those with disease involving the central nervous system; (4) Prior other malignancies (except cured basal cell carcinoma or squamous cell carcinoma of the skin, or melanoma of the skin or carcinoma in situ of the cervix) (5) Comorbidities with significantly poorly controlled conditions that may affect compliance with the study protocol, such as severe cardiovascular disease, peripheral or central nervous system disease (6) Those with positive HCV antibodies and a qualitative HCV-RNA test ≥ 104 copies/mL; or HBV test results: HBsAg positive and/or HBcAb positive and HBV DNA titers above 1000 IU/mL or 1000 copies/mL (7) Have uncontrolled heart disease, including unstable angina, acute myocardial infarction within 6 months prior to the first dose, congestive heart failure (NYHA) cardiac function class III or IV; or cardiac left ventricular ejection fraction <50%; (8) A history of immunodeficiency, including those who are HIV positive or have other acquired or congenital immunodeficiency diseases or a history of organ transplantation (9) Patients who, in the opinion of the investigator, are not suitable for enrollment. |
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研究实施时间: Study execute time: |
从 From 2023-03-01 00:00:00至 To 2025-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-08-19 00:00:00 至 To 2024-10-15 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: |
正在进行 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: |
无 |
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Blinding: |
none |
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是否共享原始数据: IPD sharing |
否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): |
EDC平台名称为Clinflash EDC(易迪希),链接为: https://edc.clinflash.com/ |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
On-demand publication in the official database of the publisher of the article after publication |
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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: |
采用电子病例记录表和电子数据采集系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
using eCRF and EDC system |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |