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注册号: Registration number: |
ChiCTR1900021970 |
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最近更新日期: Date of Last Refreshed on: |
2019-06-16 10:26:26 |
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注册时间: Date of Registration: |
2019-03-18 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
贝那鲁肽注射液对照门冬胰岛素30注射液治疗二甲双胍单药血糖控制不佳的2型糖尿病患者的前瞻性、多中心、随机、开放、平行的有效性和安全性研究 |
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Public title: |
Efficacy and safety of beinaglutide (formerly known as benaglutide) versus insulin aspart 30 as add-on therapy in patients with type 2 diabetes inadequately controlled with metformin alone: a prospective, multi-centric, randomized, open-labeled, parallel-group study. |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
贝那鲁肽注射液对照门冬胰岛素30注射液治疗二甲双胍单药血糖控制不佳的2型糖尿病患者的前瞻性、多中心、随机、开放、平行的有效性和安全性研究 |
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Scientific title: |
Efficacy and safety of beinaglutide (formerly known as benaglutide) versus insulin aspart 30 as add-on therapy in patients with type 2 diabetes inadequately controlled with metformin alone: a prospective, multi-centric, randomized, open-labeled, parallel-group study. |
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研究课题代号(代码): Study subject ID: |
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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: |
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申请注册联系人: |
卢海 |
研究负责人: |
纪立农 |
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Applicant: |
Hai Lu |
Study leader: |
Linong Ji |
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申请注册联系人电话: Applicant telephone: |
+86 021 61905511 |
研究负责人电话:
Study leader's |
+86 010 88324108 |
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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: |
luhai@benemae.com |
研究负责人电子邮件: Study leader's E-mail: |
jiln@bjmu.edu.cn |
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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: |
上海市浦东周浦紫萍路908号 |
研究负责人通讯地址: |
北京市西直门南大街11号 |
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Applicant address: |
908 Ziping Road, Shanghai International Medical Park, Zhoupu, Pudong District, Shanghai, China |
Study leader's address: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
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申请注册联系人邮政编码: Applicant postcode: |
201321 |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
上海仁会生物制药股份有限公司 |
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Applicant's institution: |
Shanghai Benemae Pharmaceutical Corporation |
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研究负责人所在单位: |
北京大学人民医院 |
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Affiliation of the Leader: |
Peking University People's Hospital |
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是否获伦理委员会批准: |
是 |
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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: |
2017PHA108-003 |
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: |
北京大学人民医院医学伦理委员会 |
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Name of the ethic committee: |
Peking University People's Hospital, Ethics Committee |
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伦理委员会批准日期: Date of approved by ethic committee: |
2019-01-31 00:00:00 | ||
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伦理委员会联系人: |
丛翠翠 |
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Contact Name of the ethic committee: |
Cuicui Cong |
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伦理委员会联系地址: |
北京市西直门南大街11号 |
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Contact Address of the ethic committee: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
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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: |
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研究实施负责(组长)单位: |
北京大学人民医院 |
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Primary sponsor: |
Peking University People's Hospital |
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研究实施负责(组长)单位地址: |
北京市西直门南大街11号 |
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Primary sponsor's address: |
11 Xizhimen Street South, Xicheng District, Beijing, China |
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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: |
上海仁会生物制药股份有限公司 |
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Source(s) of funding: |
Shanghai Benemae Pharmaceutical Corporation |
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研究疾病: |
2型糖尿病 |
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Target disease: |
Type 2 Diabetes |
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研究疾病代码: |
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Target disease code: |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
IV期临床试验 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
对于二甲双胍单药血糖控制不佳的2型糖尿病患者,给予贝那鲁肽注射液联合二甲双胍治疗或门冬胰岛素30注射液联合二甲双胍治疗24周。主要目的:对照门冬胰岛素30组,评价贝那鲁肽组的有效性;次要目的:对照门冬胰岛素30组,评价贝那鲁肽组的安全性;探索目的:探索贝那鲁肽对2型糖尿病患者在血脂、肾功能方面的额外益处。 |
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Objectives of Study: |
T2DM patients who are inadequately controlled with metformin monotherapy, receive combination therapy with beinaglutide plus metformin or insulin aspart 30 plus metformin for 24 weeks. Primary objective: To evaluate the efficacy of beinaglutide compared to insulin aspart 30 as add on therapy with metformin. Secondary objective: To evaluate the safety of beinaglutide compared to insulin aspart 30 as add on therapy with metformin. Exploratory objective: To explore additional benefits of beinaglutide plus metformin in terms of blood lipids and kidney function. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
1)1型糖尿病患者; |
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Exclusion criteria: |
1)T1DM patients |
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研究实施时间: Study execute time: |
从 From 2017-10-01 00:00:00至 To 2020-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2017-10-01 00:00:00 至 To 2020-12-31 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: |
正在进行 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): |
研究者使用SAS9.4软件产生的随机表进行随机分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Randomisation will be performed using random tables generated from SAS 9.4 software by the investigator. |
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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: |
未说明 |
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Blinding: |
Not stated |
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
各临床试验研究中心; ResMan |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Each clinical trial research center; via ResMan |
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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 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |