|
注册号: Registration number: |
ChiCTR2100044249 |
|
最近更新日期: Date of Last Refreshed on: |
2021-08-30 17:14:17 |
|
注册时间: Date of Registration: |
2021-03-12 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
重组新型冠状病毒(COVID-19)疫苗(腺病毒载体)Ⅲ期临床试验方案 |
|
Public title: |
Global phase III trial of Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector) (Ad5-nCoV) in adults 18 years of age and older |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
在18岁及以上成年人中开展的重组新型冠状病毒疫苗(腺病毒载体)(Ad5-nCoV)的有效性、安全性和免疫原性的全球多中心、随机、双盲、安慰剂对照、适应性设计的Ⅲ期临床试验 |
|
Scientific title: |
A global multi-center, randomized, double-blind, placebo-controlled, adaptive designed phase III clinical trial to evaluate the efficacy, safety and immunogenicity of Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vector) in adults 18 years of age and older Recombinant Novel Coronavirus Vaccine (Adenovirus Type 5 Vec |
|
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: |
王雪 |
研究负责人: |
Scott A Halperin |
|
Applicant: |
Wang Xue |
Study leader: |
Scott A Halperin |
|
申请注册联系人电话: Applicant telephone: |
+86 022 58213600-6051 |
研究负责人电话:
Study leader's |
+902-470-8141 |
|
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: |
xue.wang@cansinotech.com |
研究负责人电子邮件: Study leader's E-mail: |
scott.halperin@dal.ca |
|
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: |
天津经济技术开发区西区南大街185号融生大厦4层 |
研究负责人通讯地址: |
5850/5980 University Avenue Halifax, NS B3K 6R8, Canada |
|
Applicant address: |
4th Floor, Biomedical Park, 185 South Avenue, TEDA West District, Tianjin, China |
Study leader's address: |
5850/5980 University Avenue Halifax, NS B3K 6R8, Canada |
|
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: |
康希诺生物股份公司 |
||
|
Applicant's institution: |
CanSino Biologics Inc. |
||
|
研究负责人所在单位: |
Canadian Center for Vaccinology Dalhousie University/IWK Health Centre |
||
|
Affiliation of the Leader: |
Canadian Center for Vaccinology Dalhousie University/IWK Health Centre |
||
|
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: |
Ref: No.4-87/NBC521-COVID-35/20/ |
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: |
National Bioethics Committee (NBC) Pakistan |
||
|
Name of the ethic committee: |
National Bioethics Committee (NBC) Pakistan |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2020-08-07 00:00:00 | ||
|
伦理委员会联系人: |
Prof. Dr. Saima Perwaiz Iqbal |
||
|
Contact Name of the ethic committee: |
Prof. Dr. Saima Perwaiz Iqbal |
||
|
伦理委员会联系地址: |
Pakistan Health Research Council, Shahrah-e-Jamhuriat, Off Constitution Avenue, Sector G-5/2, Islamabad |
||
|
Contact Address of the ethic committee: |
Pakistan Health Research Council, Shahrah-e-Jamhuriat, Off Constitution Avenue, Sector G-5/2, Islamabad |
||
|
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: |
Canadian Center for Vaccinology Dalhousie University/IWK Health Centre |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor: |
Canadian Center for Vaccinology Dalhousie University/IWK Health Centre |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
加拿大哈利法克斯大学大道 5850/5980,NS B3K 6R8 |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor's address: |
5850/5980 University Avenue Halifax, NS B3K 6R8, Canada |
||||||||||||||||||||||||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
经费或物资来源: |
自筹 |
||||||||||||||||||||||||||||||||||||||||||||
|
Source(s) of funding: |
Self-financing |
||||||||||||||||||||||||||||||||||||||||||||
|
研究疾病: |
新型冠状病毒肺炎 (COVID-19) |
||||||||||||||||||||||||||||||||||||||||||||
|
Target disease: |
Novel Coronavirus Pneumonia (COVID-19) |
||||||||||||||||||||||||||||||||||||||||||||
|
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Ad5-nCoV在接种后28天至12个月间预防病毒学确诊(PCR阳性)的 COVID-19疾病的效力(不区分严重程度)。将在试验组和对照组间比较COVID-19的发病率。评价所有受试者接种后12个月内的SAE和MAE的发生率。 |
||||||||||||||||||||||||||||||||||||||||||||
|
Objectives of Study: |
The primary efficacy objective is the efficacy of Ad5-nCoV in preventing virologically confirmed (PCR positive) COVID-19 disease occurring 28 days to 52 weeks after vaccination, regardless of severity. COVID-19 disease rates in Ad5-nCoV group will be compared with COVID-19 rates in the control group.The primary safety objective is to evaluate the incidence of serious adverse events (SAE) and medically attended adverse events (MAE) within 52 weeks after vaccination in all participants. |
||||||||||||||||||||||||||||||||||||||||||||
|
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: |
研究过程中,受试者使用了COVID-19预防性药物。注意:由于感染COVID-19而住院的受试者可以参加COVID-19治疗性的试验,但需第一时间通知研究团队。 |
||||||||||||||||||||||||||||||||||||||||||||
|
Exclusion criteria: |
1. Participation in any other COVID-19 prophylactic drug trials for the duration of the study. Note: Participation in COVID-19 treatment trials is allowed in the event of hospitalization due to COVID-19. The study team should be informed as soon as possible; |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2020-09-22 00:00:00至 To 2022-02-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-09-22 00:00:00 至 To 2022-02-01 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): |
中央随机系统(IWRS)将用于全球临床试验受试者的随机入组。该系统会根据不同研究中心的实际情况(例如COVID-19罹患率等),在试验过程中动态调整样本量分布。将受试者随机分到试验组和对照组,比例为1:1 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
An interactive web response system (IWRS) will be used to randomize participants in global clinical trial. This system will be able to dynamically adjust the distribution of sample size according to the actual situation in different sites (such as COVID-19 attack rate, etc.) during the trial.Participants will b |
||||||||
|
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: |
Not stated |
|
Blinding: |
Not stated |
|
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): |
根据要求 请阅读网页注册指南中关于 原始数据共享 的内容。 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Open upon request |
|
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: |
EDC 系统 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC system |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |