|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2100046907 |
|
最近更新日期: Date of Last Refreshed on: |
2021-05-30 10:11:30 |
|
注册时间: Date of Registration: |
2021-05-30 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
一项评价重组人促甲状腺素注射液(SNA001)在分化型甲状腺癌(DTC)患者术后清甲治疗中安全性和有效性的随机、开放、多中心、对照的Ⅲ期临床试验(TRESON-01) |
|
Public title: |
A randomized, open-lable, multicenter, controlled phase III clinical trial to evaluate the safety and efficacy of recombinant human thryoid stimulating hormone (SNA001) in postoperative RAI treatment of differentiated thyroid cancer patients |
|
注册题目简写: |
|
|
English Acronym: |
SNA001 Phase III |
|
研究课题的正式科学名称: |
一项评价重组人促甲状腺素注射液(SNA001)在分化型甲状腺癌(DTC)患者术后清甲治疗中安全性和有效性的随机、开放、多中心、对照的Ⅲ期临床试验(TRESON-01) |
|
Scientific title: |
A randomized, open-lable, multicenter, controlled phase III clinical trial to evaluate the safety and efficacy of recombinant human thryoid stimulating hormone (SNA001) in postoperative RAI treatment of differentiated thyroid cancer patients |
|
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: |
田恒勇 |
研究负责人: |
刘斌 |
|
Applicant: |
Tian Hengyong |
Study leader: |
Liu Bin |
|
申请注册联系人电话: Applicant telephone: |
+86 13675202679 |
研究负责人电话:
Study leader's |
+86 18980606827 |
|
申请注册联系人传真 : Applicant Fax: |
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: |
hy.tian@smartnucl.com |
研究负责人电子邮件: Study leader's E-mail: |
binl@foxmail.com |
|
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): |
||
|
申请注册联系人通讯地址: |
中国苏州工业园区星湖街218号生物医药产业园A4-201 |
研究负责人通讯地址: |
四川省成都市武侯区国学巷37号 |
|
Applicant address: |
218 XingHu St.bioBAY A4-201, SuZhou lndustrial Park, Suzhou, Jiangsu, China |
Study leader's address: |
37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
|
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: |
||
|
申请人所在单位: |
苏州智核生物医药科技有限公司 |
||
|
Applicant's institution: |
Suzhou SmartNuclide Biotech Co.,Ltd. |
||
|
研究负责人所在单位: |
四川大学华西医院 |
||
|
Affiliation of the Leader: |
West China Hospital, Sichuan University |
||
|
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: |
2020临床试验(西药)审(32)号 |
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: |
四川大学华西医院临床试验伦理审查委员会 |
||
|
Name of the ethic committee: |
Clinical Trial Ethics Committee of West China Hospital, Sichuan University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2020-05-18 00:00:00 | ||
|
伦理委员会联系人: |
李娜 |
||
|
Contact Name of the ethic committee: |
Pang Zhao |
||
|
伦理委员会联系地址: |
四川省成都市武侯区国学巷37号四川大学华西医院 |
||
|
Contact Address of the ethic committee: |
Room 412, Old Eighth Building, West China Hospital, Sichuan University, 37 Guoxue Lane, Wuhou District, Chengdu, Sichuan, China |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 28 85422851 |
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: |
复旦大学附属中山医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Zhongshan Hospital of Fudan University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
上海市徐汇区枫林路180号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
180 Fenglin Road, Xuhui Dsitrict, Shanghai, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
苏州智核生物医药科技有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Suzhou SmartNuclide Biotech Co.,Ltd. |
||||||||||||||||||||||
|
研究疾病: |
分化型甲状腺癌 |
||||||||||||||||||||||
|
Target disease: |
differentiated thyroid cancer |
||||||||||||||||||||||
|
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: |
主要目的:评价SNA001在清甲治疗中的疗效非劣效于目前临床常规应用的停服甲状腺激素疗法(THW); 次要目的:观察SNA001在DTC患者术后清甲治疗中的安全性和免疫原性。 |
||||||||||||||||||||||
|
Objectives of Study: |
Primary Purpose: Evaluation of SNA001 effectiveness non-inferior to thyroid hormone withdrawal used by clinical practice during thyroid ablation; Secondary Purpose: Safety and immunogenicity of SNA001 after postoperative ablation treatment in DTC patients. |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||
|
纳入标准: |
1)签署知情同意时,年龄18-70岁(包括边界值),性别不限; |
||||||||||||||||||||||
|
Inclusion criteria |
1) Range of age was 18-70 years(boundary value included), male and female, when signing informed consent form; |
||||||||||||||||||||||
|
排除标准: |
1)预计生存时间<12个月者; |
||||||||||||||||||||||
|
Exclusion criteria: |
1) Estimated survival time < 12 months; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2020-02-20 00:00:00至 To 2022-01-06 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-03-10 00:00:00 至 To 2021-01-29 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: |
结束 /Completed |
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): |
本试验采用分层区组随机化方法,根据甲状腺癌TNM分期进行分层。按1:1的比例将受试者随机分为试验组和对照组,采用临床试验中央随机系统(DAS for IWRS)分配随机号。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
According to TNM staging of thyroid cancer, stratified block randomization method was used in this study. Subjects were divided into the experiment and control group followed the ratio of 1:1. Random number of subjects was assigned by DAS for IWRS. |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
|
盲法: |
|
|
Blinding: |
|
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): |
药物临床试验登记与信息公示平台 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
http://www.chinadrugtrials.org.cn/index.html |
|
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: |
电子采集和管理系统 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture(EDC) |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |