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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: |
ChiCTR2100049585 |
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最近更新日期: Date of Last Refreshed on: |
2021-08-05 04:01:16 |
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注册时间: Date of Registration: |
2021-08-05 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: |
硼替佐米联合化疗治疗难治/复发儿童急性淋巴细胞白血病的有效性、安全性及群体药代动力学随机对照多中心研究 |
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Public title: |
Efficacy, Safety and Population Pharmacokinetics of Bortezomib Combined with Chemotherapy in children with Refractory/Relapsed Acute Lymphoblastic Leukemia: a Multicenter, Randomized controlled Study |
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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: |
硼替佐米联合化疗治疗难治/复发儿童急性淋巴细胞白血病的有效性、安全性及群体药代动力学随机对照多中心研究 |
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Scientific title: |
Efficacy, Safety and Population Pharmacokinetics of Bortezomib Combined with Chemotherapy in children with Refractory/Relapsed Acute Lymphoblastic Leukemia: a Multicenter, Randomized controlled 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: |
付金秋 |
研究负责人: |
鞠秀丽 |
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Applicant: |
Fu Jinqiu |
Study leader: |
Ju Xiuli |
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申请注册联系人电话: Applicant telephone: |
+86 18560088120 |
研究负责人电话:
Study leader's |
+86 18560086337 |
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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: |
fjq818@163.com |
研究负责人电子邮件: Study leader's E-mail: |
shellysdcn@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: |
山东省济南市历下区文化西路107号 |
研究负责人通讯地址: |
山东省济南市历下区文化西路107号 |
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Applicant address: |
107 West Wenhua Road, Lixia District, Ji'nan, Shandong, China |
Study leader's address: |
107 West Wenhua Road, Lixia District, Ji'nan, Shandong, 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: |
山东大学齐鲁医院 |
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Applicant's institution: |
Qilu Hospital of Shandong University |
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研究负责人所在单位: |
山东大学齐鲁医院 |
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Affiliation of the Leader: |
Qilu Hospital of Shandong University |
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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: |
KYLL-2020(KS)-677 |
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: |
山东大学齐鲁医院科研伦理委员会 |
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Name of the ethic committee: |
Research Ethics Committee of Qilu Hospital, Shandong University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-05-21 00:00:00 | ||
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伦理委员会联系人: |
陈晓阳 |
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Contact Name of the ethic committee: |
Chen xiaoyang |
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伦理委员会联系地址: |
山东省济南市历下区文化西路107号 |
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Contact Address of the ethic committee: |
107 West Wenhua Road, Lixia District, Ji'nan, Shandong, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
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: |
山东大学齐鲁医院 |
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Primary sponsor: |
Qilu Hospital of Shandong University |
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研究实施负责(组长)单位地址: |
山东省济南市历下区文化西路107号 |
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Primary sponsor's address: |
107 West Wenhua Road, Lixia District, Ji'nan, Shandong, 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: |
山东大学 |
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Source(s) of funding: |
Shandong University |
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研究疾病: |
儿童白血病 |
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Target disease: |
Childhood leukemia |
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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: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
主要研究目的 硼替佐米联合再诱导方案化疗可有效提高难治/复发儿童ALL的早期分子生物学水平CR率,延长其生存时间,同时也为有条件进行HSCT的患儿争取时间。 次要研究目的 1.评价硼替佐米在儿童难治/复发ALL患者中个体化治疗的安全性; 2.研究儿童难治/复发ALL患者硼替佐米代谢产物与不良事件之间的剂量-浓度-反应关系; 3.建立中国儿童复发/难治ALL患者基因型与硼替佐米代谢产物及其引起不良反应风险之间的关联。 |
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Objectives of Study: |
Main Study Objective To assess bortezomib combined with induction chemotherapy can effectively improve the complete remission rate of children with refractory/relapsed ALL. Secondary Study Objective 1.To assess the safety of bortezomib in children with refractory/relapsed ALL; 2.To research the dose-concentration-response relationship between bortezomib metabolites and adverse events in children with refractory/relapsed ALL. 3.To establish the association between genotype and the risk of adverse reactions of bortezomib in children with relapsed/refractory ALL of China. |
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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)急性淋巴细胞白血病; |
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Inclusion criteria |
Acute lymphoblastic leukemia patients aged from 1 month old ~18 years old. |
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排除标准: |
(1)成熟B-ALL、混合表型白血病(不包括ALL伴有髓系抗原表达) |
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Exclusion criteria: |
(1) Mature B-ALL, mixed phenotypic leukemia (excluding ALL associated with myeloid antigen expression) |
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研究实施时间: Study execute time: |
从 From 2020-09-01 00:00:00至 To 2023-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-09-30 00:00:00 至 To 2023-07-31 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): |
计算机生成随机数字表 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Computer-generated sequence of numbers |
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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: |
公开/Public |
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盲法: |
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Blinding: |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
公开原始数据日期:2024.1.1 公开原始数据方式:山东大学齐鲁医院临床研究中心 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Date of original data disclosure: 2024.1.1 Original data disclosure: Clinical Research Center of Qilu Hospital, Shandong University |
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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: |
采用病例记录表(Case Record Form, CRF) |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form, CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |