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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: |
ChiCTR2100047316 |
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最近更新日期: Date of Last Refreshed on: |
2022-01-03 18:27:26 |
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注册时间: Date of Registration: |
2021-06-12 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: |
一项在中国近期发生急性冠脉综合征的人群中基于真实世界证据评价阿利西尤单抗有效性和安全性的前瞻性、多中心、观察性研究 |
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Public title: |
A real-world evidence based, prospective, multicenter, observational study on effectiveness and safety of alirocumab in a population with recent acute coronary syndrome in China |
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注册题目简写: |
REALITY |
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English Acronym: |
REALITY |
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研究课题的正式科学名称: |
一项在中国近期发生急性冠脉综合征的人群中基于真实世界证据评价阿利西尤单抗有效性和安全性的前瞻性、多中心、观察性研究 |
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Scientific title: |
A real-world evidence based, prospective, multicenter, observational study on effectiveness and safety of alirocumab in a population with recent acute coronary syndrome in China |
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研究课题代号(代码): Study subject ID: |
OBS16580 |
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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: |
NA |
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申请注册联系人: |
张倩怡 |
研究负责人: |
何静 |
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Applicant: |
Zhang Qianyi |
Study leader: |
He Jing |
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申请注册联系人电话: Applicant telephone: |
+86 18710093058 |
研究负责人电话: Study leader's telephone: |
+86 17316108216 |
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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: |
Qianyi.zhang@sanofi.com |
研究负责人电子邮件: Study leader's E-mail: |
Meredith.he@sanofi.com |
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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: |
北京市朝阳区建外大街112号 |
研究负责人通讯地址: |
北京市朝阳区建外大街112号 |
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Applicant address: |
112 Jian Guo Avenue, Chaoyang District, Beijing, China |
Study leader's address: |
112 Jian Guo Avenue, Chaoyang District, Beijing, China |
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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: |
赛诺菲(中国)投资有限公司上海分公司 |
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Applicant's institution: |
Sanofi (China) Investment Co., Ltd. Shanghai Branch |
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研究负责人所在单位: |
赛诺菲(中国)投资有限公司上海分公司 |
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Affiliation of the Leader: |
Sanofi (China) Investment Co., Ltd. Shanghai B |
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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: |
B2021-166R |
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: |
复旦大学附属中山医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Zhongshan Hospital, Fudan University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2021-04-20 00:00:00 |
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伦理委员会联系人: |
杨老师 |
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Contact Name of the ethic committee: |
Yang |
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伦理委员会联系地址: |
上海市徐汇区枫林路180号 |
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Contact Address of the ethic committee: |
180 Fenglin Road, Xuhui District, Shanghai |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 31587871 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
ec@zs-hospital.sh.cn |
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研究实施负责(组长)单位: |
复旦大学附属中山医院 |
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Primary sponsor: |
Zhongshan Hospita, Fudan University |
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研究实施负责(组长)单位地址: |
上海市徐汇区枫林路180号 |
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Primary sponsor's address: |
180 Fenglin Road, Xuhui District, Shanghai |
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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: |
赛诺菲(中国)投资有限公司 |
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Source(s) of funding: |
Sanofi (China) Investment Co., Ltd. |
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Target disease: |
Cardiovascular diseases |
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Target disease code: |
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研究类型: |
观察性研究 |
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Study type: |
Observational study |
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研究所处阶段: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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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: |
评价急性冠脉综合征接受阿利西尤单抗治疗的有效性和安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of alisumab in the treatment of acute coronary syndrome. |
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药物成份或治疗方案详述: |
仅由研究者负责开具治疗处方。 将从研究入组时已接受阿利西尤单抗治疗的患者或研究者已决定为其处方阿利西尤单抗(与研究入组无关)的患者中选择进入本研究的受试者。患者将继续/终止治疗,具体取决于观察期间治疗医生的处方和建议(与研究入组无关)。因此,赛诺菲将不会提供治疗。 治疗将由治疗医生按照常规实践进行管理/修改/处方。将针对每例患者的具体需求和当地标准诊疗常规,根据常规实践和研究者判断对降脂治疗进行个体化调整。研究者应参考当地产品说明书,以获取有关处方治疗的信息。 |
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Description for medicine or protocol of treatment in detail: |
The prescription of therapies is under the only responsibility of the Investigator. The participants who are enrolled in the study will be selected among the patients who are already treated with alirocumab at study entry, or for whom the Investigator has decided to prescribe alirocumab independently from study entry. The patients will continue/discontinue their treatment; according to the prescription and recommendation from their treating physician during the observational period, independently from study entry. Therefore, the treatment will not be provided by Sanofi. The treatment will be managed/modified/prescribed as per routine practice by the treating physician. Adjustments of lipid lowering therapies will be done as per usual practice and Investigators judgment, on an individual basis according to each patients specific needs and local standard of care. The Investigator should refer to local labeling of the product for any information on treatment prescribed. |
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纳入标准: |
1.近期(开始阿利西尤单抗治疗前52周内)因ACS住院; |
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Inclusion criteria |
1. Recent (within 52 weeks of alirocumab treatment initiation) ACS requiring hospitalization; |
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排除标准: |
1.入组前28天或5个半衰期内(以时间较长者为准)接受过其他前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂和其他试验药物治疗; |
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Exclusion criteria: |
1. Reated with other proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor and other investigational drug within 28 days or five half-lives before inclusion, whichever is longer; |
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研究实施时间: Study execute time: |
从 From 2021-07-01 00:00:00至 To 2026-01-02 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2021-07-01 00:00:00 至 To 2023-08-30 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): |
无 |
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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: |
不公开/Private |
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盲法: |
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Blinding: |
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是否共享原始数据: IPD sharing |
No |
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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): |
Sanofi.com |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Sanofi.com |
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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和EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF和EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |