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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: |
ChiCTR2400090947 |
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最近更新日期: Date of Last Refreshed on: |
2024-10-16 15:34:17 |
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注册时间: Date of Registration: |
2024-10-16 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: |
维奈克拉联合中剂量阿糖胞苷作为Fit AML患者标准诱导化疗后巩固治疗的多中心、前瞻性、观察性临床研究 |
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Public title: |
Venetoclax combined with medium-dose cytarabine as consolidation therapy after standard induction chemotherapy in patients with Fit AML: a multicenter, prospective, observational clinical 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: |
维奈克拉联合中剂量阿糖胞苷作为Fit AML患者标准诱导化疗后巩固治疗的多中心、前瞻性、观察性临床研究 |
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Scientific title: |
Venetoclax combined with medium-dose cytarabine as consolidation therapy after standard induction chemotherapy in patients with Fit AML: a multicenter, prospective, observational clinical 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: |
马赛 |
研究负责人: |
陈春燕 |
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Applicant: |
Sai Ma |
Study leader: |
Chunyan Chen |
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申请注册联系人电话: Applicant telephone: |
+86 185 6008 4816 |
研究负责人电话: Study leader's telephone: |
+86 185 6008 7023 |
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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: |
masai@qiluhospital.com |
研究负责人电子邮件: Study leader's E-mail: |
chency@sdu.edu.cn |
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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: |
No. 107 Wenhua West Road, Lixia District, Jinan City, Shandong Province |
Study leader's address: |
No. 107 Wenhua West Road, Lixia District, Jinan City, Shandong Province |
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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/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: |
KYLL-202404-014-1 |
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: |
Qilu Hospital of Shandong University Science Research Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-05-06 00:00:00 |
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伦理委员会联系人: |
陈慧 |
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Contact Name of the ethic committee: |
Hui Chen |
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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: |
No. 107 Wenhua West Road, Lixia District, Jinan City, Shandong Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 185 6008 9579 |
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: |
No. 107 Wenhua West Road, Lixia District, Jinan City, Shandong Province |
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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-financing |
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Target disease: |
AML |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
队列研究 |
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Study design: |
Cohort study |
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研究目的: |
探究维奈克拉联合中剂量阿糖胞苷作为fit AML患者缓解后巩固治疗的清除残留白血病(MRD)有效性及安全性。 |
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Objectives of Study: |
To investigate the efficacy and safety of Venetoclax combined with medium-dose cytarabine as post-remission consolidation therapy for clearance of Minimal Residual Disease (MRD) in patients with fit AML. |
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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18-59岁,男女不限 2: 可以耐受强化疗的AML(非APL)成年患者,经过诱导化疗后达到CR/CRi,但MRD阳性,使用维奈克拉联合中剂量阿糖胞苷进行巩固治疗 3: 患者伴有FLT3突变,可以加用针对性靶向药进行治疗 4: 受试者自愿签署知情同意书 |
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Inclusion criteria |
1: Age 18-59, male and female. 2: Adult patients with AML (non-APL) who can tolerate intense chemotherapy and who have achieved CR/CRi after induction chemotherapy but MRD-positive are treated with consolidation therapy using Venetoclax in combination with medium-dose cytarabine. 3: Patients with concomitant FLT3 mutations can be treated with the addition of targeted agents. 4: Subjects voluntarily sign an informed consent form. |
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排除标准: |
1: 患者患有骨髓增殖性肿瘤(MPN)病史,包括骨髓纤维化、原发性血小板增多症、真性红细胞增多症、慢性粒细胞白血病(CML)以及伴有BCR-ABL1易位的AML或急性早幼粒细胞白血病(APL) 2: 有MDS病史的继发AML 3: 患有活动性的白血病中枢神经系统浸润 4: 临床上未能控制的活动性感染及脏器出血 5: 合并重要脏器功能严重异常及其他恶性肿瘤 6: 会妨碍研究参与的精神障碍 7: 妊娠或哺乳期的患者 |
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Exclusion criteria: |
1: Patients have a history of myeloproliferative neoplasms (MPN), including myelofibrosis, essential thrombocythemia, true erythrocytosis, chronic myelogenous leukemia (CML), and AML with BCR-ABL1 translocation or acute promyelocytic leukemia (APL). 2: Secondary AML with a history of MDS 3: Central nervous system infiltration with active leukemia 4: Clinically uncontrolled active infection and organ hemorrhage 5: Combination of severe abnormalities of vital organ function and other malignant tumors 6: Mental disorders that would prevent research participation 7: Patients who are pregnant or breastfeeding |
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研究实施时间: Study execute time: |
从 From 2024-11-01 00:00:00至 To 2027-11-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-11-01 00:00:00 至 To 2027-11-01 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: |
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 |
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): |
不共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
not sharing |
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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: |
病例记录表 |
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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 |
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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 |