|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR-TRC-11001539 |
|
最近更新日期: Date of Last Refreshed on: |
2017-01-24 14:42:34 |
|
注册时间: Date of Registration: |
2011-08-12 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
苏粒佳(重组人血管内皮抑素注射液)联合化疗及苏粒佳维持治疗治疗非小细胞肺癌患者的III期临床试验 |
|
Public title: |
Recombinant endostatin (Sulijia) combined chemotherapy with Vinorelbine and Cisplatin (NP) plus maintenance therapy with Sulijia for advanced Non-small Cell Lung Cancer: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III trial |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
随机、双盲、多中心评价苏粒佳?(重组人血管内皮抑素注射液)联合长春瑞滨和顺铂(NP)对照安慰剂联合NP及苏粒佳?维持治疗治疗初治的晚期非小细胞肺癌患者疗效和安全性的Ⅲ期临床研究 |
|
Scientific title: |
Recombinant endostatin ( Sulijia) combined chemotherapy with Vinorelbine and Cisplatin (NP) plus maintenance therapy with Sulijia for advanced Non-small Cell Lung Cancer: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III trial |
|
研究课题代号(代码): Study subject ID: |
WZYY2011003 |
|
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: |
杨南林 |
研究负责人: |
石远凯 |
|
Applicant: |
Nanlin Yang |
Study leader: |
Yuankai Shi |
|
申请注册联系人电话: Applicant telephone: |
+86 0512 65686211 |
研究负责人电话:
Study leader's |
+86 010 67781331 |
|
申请注册联系人传真 : Applicant Fax: |
+86 0512 65686186 |
研究负责人传真: Study leader's fax: |
+86 010 67705068 |
|
申请注册联系人电子邮件: Applicant E-mail: |
yangnanlin@163.com |
研究负责人电子邮件: Study leader's E-mail: |
syuankai@yahoo.cn |
|
申请单位网址(自愿提供): Applicant website(voluntary supply): |
www.wzyy.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: |
江苏省苏州市吴中区东方大道988号18楼 |
研究负责人通讯地址: |
北京市朝阳区潘家园南里17号中国医学科学院肿瘤医院 |
|
Applicant address: |
18th Floor, 988 Dongfang Avenue, Wuzhong, Suzhou, Jiangsu, China |
Study leader's address: |
17 Panjiayuan Nanli, Chaoyang District, Beijing, China |
|
申请注册联系人邮政编码: Applicant postcode: |
215124 |
研究负责人邮政编码: Study leader's postcode: |
100021 |
|
申请人所在单位: |
江苏吴中医药集团有限公司 |
||
|
Applicant's institution: |
Jiangsu Wuzhong Pharmaceutical Group Inc |
||
|
研究负责人所在单位: |
|
||
|
Affiliation of the Leader: |
|
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
11-59/494 |
伦理委员会批件附件: Approved file of Ethical Committee: |
|
|
批准本研究的伦理委员会名称: |
中国医学科学院肿瘤医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethic Committee of Cancer Institute & Hospital Chinese Academy of Medical Science |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2011-09-27 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: |
中国医学科学院肿瘤医院 |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor: |
Cancer Institute & Hospital Chinese Academy of Medical Science |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
北京市朝阳区潘家园南里17号 |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor's address: |
17 Panjiayuan Nanli, Chaoyang District, Beijing |
||||||||||||||||||||||||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
经费或物资来源: |
江苏吴中医药集团有限公司 |
||||||||||||||||||||||||||||||||||||||||||||
|
Source(s) of funding: |
Jiangsu Wuzhong Pharmaceutical Group Inc. |
||||||||||||||||||||||||||||||||||||||||||||
|
研究疾病: |
晚期非小细胞肺癌 |
||||||||||||||||||||||||||||||||||||||||||||
|
Target disease: |
Advanced or metastatic (IV) NSCLC |
||||||||||||||||||||||||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
研究类型: |
干预性研究 |
||||||||||||||||||||||||||||||||||||||||||||
|
Study type: |
Interventional study |
||||||||||||||||||||||||||||||||||||||||||||
|
研究所处阶段: |
III期临床试验 | ||||||||||||||||||||||||||||||||||||||||||||
|
Study phase: |
3 |
||||||||||||||||||||||||||||||||||||||||||||
|
研究设计: |
随机平行对照 |
||||||||||||||||||||||||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||||||||||||||||||||||||
|
研究目的: |
评价苏粒佳?联合长春瑞滨和顺铂(NP)对照安慰剂联合NP及苏粒佳?维持治疗治疗初治的晚期非小细胞肺癌患者的临床生存期获益优势 |
||||||||||||||||||||||||||||||||||||||||||||
|
Objectives of Study: |
The main object of this trial is to offer treatment of recombinant endostatin ( Sulijia?) combined with Vinorelbine and Cisplatin (NP) plus maintenance therapy with Sulijia? for advanced Non-small Cell Lung Cancer, expecting to improve progression free survival (PFS) and Overall survival (OS) compared with chemotherapy alone, and evaluate the efficacy of Sulijia. |
||||||||||||||||||||||||||||||||||||||||||||
|
药物成份或治疗方案详述: |
重组人血管内皮抑素 1mg/ml |
||||||||||||||||||||||||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
rh-Endostatin 1mg/ml |
||||||||||||||||||||||||||||||||||||||||||||
|
纳入标准: |
(1)年龄18~70周岁,性别不限;(2)经组织学确诊的初治Ⅳ期NSCLC患者(参照UICC第七版分期标准);(3) 根据RECIST标准至少有一个可测量病灶;通过以下任何方法至少可精确测量病灶单径者,胸部或腹部计算机断层扫描(CT),常规方法直径至少20mm或应用螺旋CT直径至少10mm。(4) 体力状况ECOG评分(PS)为0~1;(5) 预计生存时间至少12周;(6) 器官功能水平必须符合下列要求:外周血:中性粒细胞绝对计数(ANC) ≥ 1.5 × 109 / L,血小板 ≥ 90 × 109 / L,血红蛋白≥9 g/dL;肝脏:胆红素≤2倍正常值上限,天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)≤2.5倍正常值上限(如果有肝转移时允许AST,ALT≤5倍正常值上限);肾脏:血清肌酐清除率≥正常值范围的80%(毫升/每分);(7)能理解本试验并已签署知情同意书者。 |
||||||||||||||||||||||||||||||||||||||||||||
|
Inclusion criteria |
1. Male and female aged 18 to 70 years old; |
||||||||||||||||||||||||||||||||||||||||||||
|
排除标准: |
(1)对目前或既往诊断的NSCLC进行过任何全身性抗癌治疗,包括细胞毒性药物治疗、靶向药物治疗、试验药物治疗、抗癌中药治疗的患者;(2)脑转移患者;(3) 在本研究的治疗开始前五年内患有除NSCLC以外的其它癌症的患者。除外已治愈的宫颈原位癌、基底细胞癌;(4)妊娠、哺乳期妇女; (5)有活动性感染性疾病的病人;(6)有症状的心律失常、不稳定的心绞痛和不可控制的高血压的患者;(7)有静脉血栓形成病史的患者;(8)有精神病病史的患者;(9)对大肠杆菌基因工程产品过敏患者;(10)研究者认为不宜参加本试验者.1 |
||||||||||||||||||||||||||||||||||||||||||||
|
Exclusion criteria: |
1. Receive the treatment of other experimental trials in the same period; on the medication of other anticancer drugs at the same time; |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2011-08-01 00:00:00至 To 2015-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2011-09-01 00:00:00 至 To 2014-09-21 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
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): |
计算机软件 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
computer generated |
||||||||
|
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: |
统计学家 双盲 |
|
Blinding: |
Statisticion Blinding |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
否No |
|
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): |
泰格医药科技股份有限公司 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Tigermed Consulting Co.,LTD |
|
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: |
泰格医药科技股份有限公司 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Tigermed Consulting Co.,LTD |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |