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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: |
ChiCTR1900021970 |
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最近更新日期: Date of Last Refreshed on: |
2019-06-05 15:01:37 |
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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: |
2017PHA108-01 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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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: |
2018-01-17 00:00:00 | ||
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伦理委员会联系人: |
王方 |
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Contact Name of the ethic committee: |
Fang Wang |
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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: |
1)受试者自愿签署知情同意书;2)年龄为18~75岁(含);3)男性或非妊娠、非哺乳期女性;4)诊断为2型糖尿病(T2DM)的受试者(符合1999年WHO标准),6个月≤病程<10年;5)受试者体重指数(BMI):21 kg/m2≤BMI≤40kg/m2;6)受试者血糖控制不佳,定义为7.5% ≤ HbA1c ≤ 10%(筛选当日前14天内检查结果有效);7)筛选前3个月内受试者接受口服二甲双胍单药治疗,治疗剂量≥1000mg/天,且剂量稳定3个月以上; 8)根据研究者的判断,患者能够并且愿意履行如下方面:(1)在整个研究期间,根据方案的规定持续研究治疗;(2)参加定期的访视,并且愿意接受电话随访;(3)有生育可能的女性受试者(以及女方有生育可能的男性受试者)在整个研究期间采取有效的避孕措施。 |
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Inclusion criteria |
1. Subjects voluntarily sign the informed consent; |
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排除标准: |
1)1型糖尿病患者;2)对贝那鲁肽、门冬胰岛素30,或任一组分过敏或有使用禁忌症者或不耐受者; 3)在筛选前6个月内,受试者发生过3次以上严重低血糖;4)在筛选前3 个月内,受试者体重变化大于10%; 5)糖尿病酮症酸中毒或高渗性非酮症昏迷患者;6) 已知患有增殖性视网膜病或黄斑病变,研究者判断需要紧急治疗;7)可能会影响 HbA1c 测量值的任何血液疾病,如:血红蛋白病病史、慢性贫血(男性≤120g/L ,女性≤110g/L ); 8)受试者有明显的肝脏疾病的临床症状或体征,急性或慢性肝炎,或筛选访视时 ALT/AST水平≥正常值上限的 3倍 ;9)肾移植病史、正在接受肾透析者、或男性血清肌酐水平≥1.5 mg/dL(133 μmol/L),女性血清肌酐水平≥1.4mg/dL(124μmol/L) ;10)梗阻性肠道疾病病史;明确胰腺炎病史; 11)在筛选访视前 3 个月内出现过以下任一心血管疾病:急性心肌梗死、根据纽约心脏病协会心功能分级 III/IV 级或左室射血分数≤40%的充血性心力衰竭或脑血管事件(卒中); 12) 未能得到良好控制的顽固性高血压(收缩压≥180 mmHg或舒张压≥105 mmHg);13)合并有下列疾病者:前庭疾病、恶性肿瘤、活动结核者; 14) 应激状态如手术、急性颅脑损伤等;15)筛选前3个月内使用过减重药物,包括但不限于处方药或中草药; 16)正在接受治疗胃肠道疾病治疗,使用直接影响胃肠蠕动的药物(如甲氧氯普胺,西沙必利和大环内酯类抗生素);17) 正在接受慢性(持续2周以上)全身性糖皮质激素治疗(不包括局部用药和吸入制剂)或在研究开始前2周内接受此类治疗;18)可能会妨碍患者遵循和完成试验方案的任何其他情况(如已知的吸毒、酗酒、精神疾病等); 19)目前正在参加或入组前 30 天内刚停止了一项涉及研究药物的或未被批准使用的药物或器械的临床试验;或同时参加其他类型的医学研究经研究者从医学或科学的角度判断不适合参加本研究; 20)之前从本试验或其它GLP-1受体激动剂试验退出的受试者;21)其他研究者认为不适合进行试验的原因。 |
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Exclusion criteria: |
1)T1DM2)History of intolerance or allergic reactions to or contraindication for beinaglutide / insulin aspart 30 3)Histories of severe hypoglycemia (≥3 times) within 6 months before the screening4)History of weight change over 10% for the last 3 months before the screening 5) Diabetic ketoacidosis or hyperosmolar nonketotic coma patients;6)Known to have proliferative retinopathy or maculopathy which needs an urgent treatment by the investigator's judgment;7)Hematological system diseases which maybe affect HbA1c value,such as: History of hemoglobinopathy, chronic anemia (male ≤120g/L, female ≤110g/L); 8) Impaired liver function, with obvious clinical signs or symptoms of liver disease, acute or chronic hepatitis, or ALT/AST levels ≥3.0 times of the upper limit of the reference range at the screening visit;9)History of transplant, renal dialysis, or serum creatinine ≥1.5mg/dl (133 umol/L) for male, ≥1.4mg/dl (124umol/L) for female;10)History of obstructive bowel disease; history of pancreatitis; 11)Occurring any of the following cardiovascular diseases within three months before the screening visit: acute myocardial infarction, heart function classification III/IV according to New York Heart Association, congestive heart failure with left ventricular ejection fraction ≤40%, or cerebrovascular events (apoplexy); 12) Persistent uncontrolled hypertension (systolic blood pressure ≥180mmHg, or diastolic blood pressure ≥105mmHg);13)Patients with the following diseases: vestibular diseases, malignant tumors, active tuberculosis; 14) Stress state as surgery, acute craniocerebral injury etc; 15)Use of weight loss drugs within 3 months before the screening, including but not limited to prescription drugs or herbal medicines; 16)Receiving gastrointestinal disease treatment with drugs that directly affect gastrointestinal motility (such as metoclopramide, cisapride, and macrolide antibiotics);17)Receiving long-term (>2 weeks) systemic glucocorticoid treatment (not including focal or inhalation treatment) or received this type of treatment within 2 weeks before the screening visit;18)Any conditions which may affect patients follow and complete the study protocol (as known drug abuse, alcoholic, mental diseases); 19)Currently in a study or just quit a study involving the investigational medicinal product or not approved drugs or instruments within 30 days before enrollment; or participating other types of clinical studies at the same time and not suitable to participate in this study judged by investigators from medical or science perspectives; 20)Subjects who previously withdrew from this trial or other GLP-1 receptor agonist trials;21)Any other cases which are deemed as inappropriate to participate in the study by the investigator. |
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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 |