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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: |
ChiCTR2000035100 |
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最近更新日期: Date of Last Refreshed on: |
2020-07-31 20:26:27 |
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注册时间: Date of Registration: |
1990-01-01 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: |
审核中(三)西达本胺联合沙利度胺、环磷酰胺和地塞米松(TC2D)治疗难治复发多发性骨髓瘤(MM)的前瞻性、单臂、探索性临床研究 |
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Public title: |
A prospective, single-arm, exploratory clinical study on the treatment of refractory and relapsed multiple myeloma (MM) patients with Chidamide combined with Thalidomide, Cyclophosphamide and Dexamethasone (TC2D) |
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注册题目简写: |
MM-C01 |
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English Acronym: |
MM-C01 |
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研究课题的正式科学名称: |
西达本胺联合沙利度胺、环磷酰胺和地塞米松(TC2D)治疗难治复发多发性骨髓瘤(MM)的前瞻性、单臂、探索性临床研究 |
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Scientific title: |
A prospective, single-arm, exploratory clinical study on the treatment of refractory and relapsed multiple myeloma (MM) patients with Chidamide combined with Thalidomide, Cyclophosphamide and Dexamethasone (TC2D) |
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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: |
何静松 |
研究负责人: |
蔡真 |
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Applicant: |
Jingsong He |
Study leader: |
Zhen Cai |
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申请注册联系人电话: Applicant telephone: |
13600547247 |
研究负责人电话: Study leader's telephone: |
13657190311 |
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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: |
hejingsong@zju.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
caiz@zju.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: |
浙江杭州上城区城站路58号2号楼4楼 |
研究负责人通讯地址: |
浙江杭州上城区庆春路79号2号楼19楼 |
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Applicant address: |
4th Floor, Building 2, 58 Chengzhan Road, Shangcheng District, Hangzhou, Zhejiang Province |
Study leader's address: |
19th Floor, Building 2, 79 Qingchun Road, Shangcheng District, Hangzhou, Zhejiang 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: |
浙江大学医学院附属第一医院 |
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Applicant's institution: |
The First Affiliated Hospital, College of Medicine, Zhejiang University |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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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: |
快审第(309)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: |
浙江大学医学院附属第一医院临床研究伦理委员会IIT伦理审查小组 |
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Name of the ethic committee: |
Clinical Research Ethics Committee of The First Affiliated Hospital, College of Medicine,Zhejiang University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-07-07 00:00:00 |
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伦理委员会联系人: |
殷琳 |
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Contact Name of the ethic committee: |
Lin Yin |
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伦理委员会联系地址: |
浙江杭州上城区庆春路79号4号楼1楼 |
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Contact Address of the ethic committee: |
1st Floor, Building 4, 79 Qingchun Road, Shangcheng District, Hangzhou, Zhejiang Province |
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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: |
浙江大学医学院附属第一医院 |
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Primary sponsor: |
The First Affiliated Hospital, College of Medicine, Zhejiang University |
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研究实施负责(组长)单位地址: |
浙江杭州上城区庆春路79号 |
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Primary sponsor's address: |
79 Qingchun Road, Shangcheng District, Hangzhou, Zhejiang 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-raised |
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Target disease: |
Multiple Myeloma |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
评价西达本胺联合沙利度胺、环磷酰胺和地塞米松(TC2D)方案治疗难治复发MM患者的安全性及疗效。至少一次评估为有效(SD及SD以上)患者的无疾病进展生存(PFS)和总生存(OS);治疗及疾病对患者生活质量的影响。 |
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Objectives of Study: |
The main purpose is to evaluate the safety and efficacy of chidamide combined with thalidomide, cyclophosphamide and dexamethasone (TC2D) in the treatment of patients with refractory and relapsed MM. The progression-free survival (PFS) and overall survival (OS) of patients who were assessed as effective (SD or above).and the impact of treatment and disease on the quality of life of patients will also be evaluated in this study. |
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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: |
了解并自愿签署知情同意书。年龄 ≥18 岁~75岁。根据2014年IMWG的多发性骨髓瘤诊断标准诊断为难治复发需要立即进行挽救性治疗的患者。既往曾使用硼替佐米及来那度胺治疗,且最后疗程完成后评估为疾病进展。 |
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Inclusion criteria |
Understand and sign the informed consent form voluntarily. Age ≥18 years to 75 years old. According to the 2014 IMWG diagnostic criteria, patients who are diagnosed as refractory and relapsed multiple myeloma and require immediate rescue treatment. Patients enrolled should be treated with bortezomib and lenalidomide as previous therapy, and the disease was evaluated as disease progression (PD) after the completion of the final course. |
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排除标准: |
任何能导致患者在参与这项研究时发生无法承受风险的严重疾病。需要继续积极治疗的疾病,如不稳定的心脏疾病,中风,类风湿性关节炎、狼疮等。妊娠或哺乳期女性。除MM以外的恶性肿瘤患病史,除非患者已经无该疾病生存超过3 年。随机前4周内接种过活疫苗、减毒活疫苗。 |
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Exclusion criteria: |
Any serious illness that can cause patients to suffer unbearable risks while participating in this study. Diseases that require continued active treatment, such as unstable heart disease, stroke, rheumatoid arthritis, lupus, etc. Women who are pregnant or breastfeeding. A history of malignancy other than myelomashould be excluded, unless the patient hadbeen disease free for more than 3 years.OnceVaccinated live vaccine and/or live attenuated vaccine within 4 weeks before randomization. |
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研究实施时间: Study execute time: |
从 From 2020-08-01 00:00:00至 To 2025-07-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2020-08-01 00:00:00 至 To 2022-07-31 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: |
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): |
NA |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
NA |
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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 |
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): |
http://www.medresman.org |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
http://www.medresman.org |
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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: |
CRF |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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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 |