一项复方黄黛片联合全反式维甲酸(ATRA)治疗老年骨髓增生异常综合征难治性贫血伴原始细胞增多(MDS-RAEB)的前瞻性、开放标签性、多中心临床研究

注册号:

Registration number:

ChiCTR-OPC-17011137 

最近更新日期:

Date of Last Refreshed on:

2017-04-13 11:53:26 

注册时间:

Date of Registration:

2017-04-13 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

一项复方黄黛片联合全反式维甲酸(ATRA)治疗老年骨髓增生异常综合征难治性贫血伴原始细胞增多(MDS-RAEB)的前瞻性、开放标签性、多中心临床研究

Public title:

An open-label, multicenter, prospective study for Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic Syndromes-Refractory Anemia with Excess Blasts (MDS-RAEB)

注册题目简写:

English Acronym:

研究课题的正式科学名称:

一项复方黄黛片联合全反式维甲酸(ATRA)治疗老年骨髓增生异常综合征难治性贫血伴原始细胞增多(MDS-RAEB)的前瞻性、开放标签性、多中心临床研究

Scientific title:

An open-label, multicenter, prospective study for Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic Syndromes-Refractory Anemia with Excess Blasts (MDS-RAEB)

研究课题代号(代码):

Study subject ID:

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:

申请注册联系人:

徐泽锋 

研究负责人:

肖志坚 

Applicant:

Zefeng Xu 

Study leader:

Zhijian Xiao 

申请注册联系人电话:

Applicant telephone:

+86 22 23909046

研究负责人电话:

Study leader's
telephone:

+86 22 23909184

申请注册联系人传真 :

Applicant Fax:

+86 22 27313013

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

gbxzf@163.com

研究负责人电子邮件:

Study leader's E-mail:

zjxiao@medmail.com.cn

申请单位网址(自愿提供):

Applicant website(voluntary supply):

www.chinablood.com.cn

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

天津市南京路288号

研究负责人通讯地址:

天津市南京路288号

Applicant address:

288 Nanjing Road, Tianjin, China

Study leader's address:

288 Nanjing Road, Tianjin, China

申请注册联系人邮政编码:

Applicant postcode:

300020

研究负责人邮政编码:

Study leader's postcode:

300020

申请人所在单位:

中国医学科学院血液病医院(血液学研究所)

Applicant's institution:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

研究负责人所在单位:

中国医学科学院血液病医院(血液学研究所)

Affiliation of the Leader:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

IIT2017002-EC-1

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

中国医学科学院血液病医院伦理委员会

Name of the ethic committee:

Ethics Committee of Blood Diseases Hospital, Chinese Academy of Medical Sciences

伦理委员会批准日期:

Date of approved by ethic committee:

2017-04-06 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

研究实施负责(组长)单位:

中国医学科学院血液病医院(血液学研究所)

Primary sponsor:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

研究实施负责(组长)单位地址:

天津市南京路288号

Primary sponsor's address:

288 Nanjing Road, Tianjin, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

天津市

市(区县):

Country:

China

Province:

Tianjin

City:

单位(医院):

中国医学科学院血液病医院(血液学研究所)

具体地址:

天津市南京路288号

Institution
hospital:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

Address:

288 Nanjing Road, Tianjin, China

经费或物资来源:

中国医学科学院血液病医院(血液学研究所)

Source(s) of funding:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

研究疾病:

骨髓增生异常综合征  

Target disease:

Myelodysplastic Syndromes

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

单臂 

Study design:

Single arm 

研究目的:

研究主要目的是评价复方黄黛片联合ATRA治疗老年骨髓增生异常综合征RAEB(MDS-RAEB)患者的近期疗效和安全性。研究的主要疗效指标是评价复方黄黛片联合ATRA给药方案的总体反应率(ORR=CR+PR+HI)。次要疗效指标是评价骨髓完全缓解率(mCR)、细胞遗传学缓解率、输血需求情况、住院情况、安全性和生活质量。  

Objectives of Study:

The study objectives are to assess the safety and tolerability of Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA) in old subjects with Myelodysplastic syndrome (MDS-RAEB), as well as the overall response rate according to the IWG 2006 response criteria, hematologic improvement, cytogenetic response rates, transfusion requirements, the hospitalizations and Quality of life(QOL).

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.年龄<60岁;2.30天内参加过其他的临床试验者;3.有肿瘤病史并且在过去的3年内接受过任何针对此肿瘤的治疗,但除去浅表性膀胱癌、皮肤的基底层细胞或鳞状上皮细胞癌、宫颈上皮内癌变(CIN)或前列腺上皮内癌变(PIN);4.有活动性的病毒或细菌感染,且未能用适当的抗感染治疗进行控制;5.已知艾滋病毒或活动性丙肝病毒的血清学反应为阳性;6.有未控制的心脏疾病的患者;7.患有精神疾患或其他病情而不能配合研究治疗和监测的要求;8.骨髓空抽;9.已知对砷剂或全反式维甲酸中任一成分过敏者;10.曾接受过砷剂或维甲酸治疗,或者在过去1年内接受过造血干细胞移植。

Exclusion criteria:

Potential subjects who meet any of the following criteria will be excluded from participating in the study:
1. Has received an investigational drug within 30 days preceding the first dose of study drug;
2. A history of tumor and accept any the treatment for the tumor in the past three years;
3. Has active viral or bacterial infection, and has uncontrolled infection by using appropriate anti-infection;
4. Has known positive serology for HIV;
5. Has uncontrolled heart trouble;
6. Has a mental illness or any other condition that could prevent full cooperation with the treatment and monitoring requirements of the study;
7. Has inaspirable bone marrow;
8. Has known hypersensitivity to any of the excipients of Realgar-Indigo naturalis Formula(RIF) and All-Trans-Retinoic Acid(ATRA);
9. Has previously been treated with Realgar-Indigo naturalis Formula(RIF) or All-Trans-Retinoic Acid(ATRA), or received hematopoietic stem cell transplantation in the past year.

研究实施时间:

Study execute time:

From 2017-05-01 00:00:00 To 2018-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2017-05-01 00:00:00 To 2018-06-30 00:00:00

干预措施:

Interventions:

组别:

病例系列

样本量:

30

Group:

case series

Sample size:

干预措施:

复方黄黛片联合全反式维甲酸

干预措施代码:

Intervention:

Realgar-Indigo naturalis Formula(RIF) combined with All-Trans-Retinoic Acid(ATRA)

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

天津市 

市(区县):

 

Country:

China

Province:

Tianjin

City:

单位(医院):

中国医学科学院血液病医院(血液学研究所) 

单位级别:

三级甲等医院 

Institution
hospital:

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

总体反应率

指标类型:

主要指标

Outcome:

overall response rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

骨髓缓解

指标类型:

次要指标

Outcome:

Marrow response

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

细胞遗传学缓解率

指标类型:

次要指标

Outcome:

cytogenetic response rates

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

输血情况

指标类型:

次要指标

Outcome:

transfusion requirements

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 60 years
最大 Max age years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

Randomization Procedure (please state who generates the random number sequence and by what method):

NO

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

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

是Yes

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):

中国医学科学院血液病医院(血液学研究所)

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Institute of Hematology and Blood Diseases Hospital , Chinese Academy of Medical Sciences

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:

中国医学科学院血液病医院(血液学研究所)

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Institute of Hematology and Blood Diseases Hospital , Chinese Academy of Medical Sciences

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2017-04-13 11:53:26