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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: |
ChiCTR2300072822 |
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最近更新日期: Date of Last Refreshed on: |
2023-06-26 15:00:57 |
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注册时间: Date of Registration: |
2023-06-26 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: |
rhEPO-Fc 静脉给药在施行血液透析的中国慢性肾脏病贫血患者中用于维持治疗的多中心、随机、开放、阳性药对照的 Ⅲ期临床研究 |
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Public title: |
A multicenter, randomized, open, position-controlled Phase III study of rhEPO-Fc intravenous administration for maintenance therapy in Chinese patients with chronic renal disease anemia undergoing hemodialysis |
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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: |
rhEPO-Fc 静脉给药在施行血液透析的中国慢性肾脏病贫血患者中用于维持治疗的多中心、随机、开放、阳性药对照的 Ⅲ期临床研究 |
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Scientific title: |
A multicenter, randomized, open, position-controlled Phase III study of rhEPO-Fc intravenous administration for maintenance therapy in Chinese patients with chronic renal disease anemia undergoing hemodialysis |
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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: |
王茶 |
研究负责人: |
左力 |
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Applicant: |
Wang cha |
Study leader: |
Zuo li |
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申请注册联系人电话: Applicant telephone: |
+86 185 1972 1132 |
研究负责人电话:
Study leader's |
+86 139 1002 8495 |
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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: |
wangcha@buchangbio.com |
研究负责人电子邮件: Study leader's E-mail: |
Zuolimd@hotmail.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: |
北京市大兴区亦庄宏达北路8号宏达工业园八号科技广场8406室 |
研究负责人通讯地址: |
北京市西城区西直门南大街 11 号 |
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Applicant address: |
8406, Science and Technology Plaza, 8#, Hongda Industrial Park, 8#, North Hongda Road, Yizhuang, Daxing District, Beijing |
Study leader's address: |
11 Xizhimen South Street, Xicheng District, Beijing |
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申请注册联系人邮政编码: Applicant postcode: |
100176 |
研究负责人邮政编码: Study leader's postcode: |
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申请人所在单位: |
四川泸州步长生物制药有限公司 |
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Applicant's institution: |
Sichuan Luzhou Buchang Bio-Pharmaceutical Co., Ltd. |
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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: |
2020PHC025-001 |
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: |
北京大学人民医院伦理审查委员会 |
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Name of the ethic committee: |
Ethical Review Committee of Peking University People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2021-01-22 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: |
Cong cui cui |
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伦理委员会联系地址: |
北京市西城区西直门南大街11号 |
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Contact Address of the ethic committee: |
11 Xizhimen South Street, Xicheng District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 8832 4516 |
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: |
北京市西城区西直门南大街 11 号 |
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Primary sponsor's address: |
11 Xizhimen South Street, Xicheng District, Beijing |
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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: |
四川泸州步长生物制药有限公司 |
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Source(s) of funding: |
Sichuan Luzhou Buchang Bio-Pharmaceutical Co., Ltd. |
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研究疾病: |
施行血液透析的中国慢性肾脏病贫血患者 |
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Target disease: |
Chinese chronic kidney disease anemia patients undergoing hemodialysis |
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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: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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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: |
通过rhEPO-Fc与阳性药利血宝 ? 比较,考察rhEPO-Fc在施行血液透析的中国慢性肾脏病贫血患者中用于维持治疗的有效性和安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of rhEPO-Fc for maintenance therapy in Chinese patients with chronic renal disease anemia undergoing hemodialysis by comparing rhEPO-Fc with the positive drug Rexabor ?. |
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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: |
均需满足方可入组: 1. 慢性肾衰竭患者,入选前接受充分维持性血液透析 12 周以上,每周透析治疗 2-4 次; 2. 中国公民,18~75 岁(含边界值); 3. 性别不限; 4. 入选前正在接受 ESAs 治疗,且持续至少 12 周,平均每周用药剂量 ≤ 10000IU; 5. 筛选期 6 周内,血红蛋白的检测值在随机分组前最近两次在 100~120g/L(含界值)内,检测时间至少间隔 7 天; 6. 入选前受试者的血清叶酸值 ≥ 正常值下限,维生素 B12水平 ≥ 正常值下限; 7. 血液透析受试者,使用导管为除临时导管外的其他 3 种通路; 8. 受试者自愿参加试验并签署知情同意书,能够依照试验方案规定完成研究。 |
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Inclusion criteria |
Must meet to be included in the group: 1. Patients with chronic renal failure received adequate maintenance hemodialysis for more than 12 weeks before inclusion, and dialysis treatment was performed 2-4 times per week; 2. Chinese citizens, 18-75 years old (including boundary values); 3. No gender limitation; 4. The patients were receiving ESAs treatment for at least 12 weeks before inclusion, and the average weekly dose was less than 10,000 IU; 5. Within 6 weeks of the screening period, the detection value of hemoglobin should be within 100~120g/L (including the threshold value) for the last two times before randomization, and the detection time should be at least 7 days apart; 6. The serum folic acid value and vitamin B12 level of the subjects before inclusion were ≥ the lower limit of normal value; 7. For hemodialysis subjects, the catheter should be used in three other channels except temporary catheter; 8. The subjects voluntarily participate in the experiment and sign the informed consent, and can complete the study in accordance with the experimental protocol. |
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排除标准: |
满足一项即排除: 1. 入选前血压未能得到有效的控制(舒张压 > 110 mmHg或收缩压 > 170 mmHg); 2. 入选前伴有难治性高血压患者(应用非药物治疗以及包括利尿剂在内的至少3种药物足量治疗数周仍不能将血压控制在目标水平为难治性高血压); 3. 已知患有脑血管畸形(如脑血管瘤)者; 4. 既往或目前患有恶性肿瘤者(已切除的非黑素瘤皮肤癌和原位癌除外); 5. 正患有NYHA Ⅲ级或IV级心力衰竭的患者,或心电图检查显示QTc间期 ≥ 550ms; 6. 严重的肝病病史; 7. 入选前ALT或AST超过正常值上限2倍者; 8. 入选前3个月之内接受过免疫抑制剂治疗的患者; 9. 入选前3个月内参加过其他药物临床试验或1个月内参加过医疗器械临床试验; 10. 正处于血栓栓塞性疾病急性期的患者; 11. 已知凝血障碍或患有溶血症; 12. 患有未被控制的慢性免疫性疾病(例如:风湿性关节炎、系统性红斑狼疮等); 13. 发生明显感染者或C反应蛋白 ≥ 30mg/L; 14. 处于结核病活动期的患者; 15. 妊娠、哺乳期妇女; 16. 在筛选前3个月内有消化道出血史、大量出血史或输血史者; 17. 入选前受试者的血清铁蛋白 < 100μg/L且转铁蛋白饱和度 < 20%者; 18. 入选前受试者的iPTH > 800pg/mL; 19. 筛选前3个月内合并使用铝制剂者,或所从事工作可能导致体内铝蓄积的铝工业从业人员; 20. 有明确的ESAs或rhEPO-Fc制剂辅料过敏史,或研究者判定为可能对本产品过敏的患者; 21. 正在服用抗精神病药物的患者; 22. 预期寿命小于12个月; 23. 研究者判定,不适于作为该研究的候选人的受试者(研究者认为可能对参加本试验的受试者的安全构成威胁的医学情况、可能混淆有效性或安全性评价的医学情况或可能干扰受试者参与试验的医学情况)。 |
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Exclusion criteria: |
One is excluded: 1. Blood pressure was not effectively controlled before inclusion (diastolic blood pressure > 110 mmHg or systolic blood pressure > 170 mmHg); 2. Patients with refractory hypertension prior to enrollment (refractory hypertension who could not control blood pressure at the target level after several weeks of adequate treatment with non-drug therapy and at least 3 drugs including diuretics); 3. Known cerebrovascular malformations (such as cerebral hemangioma); 4. Previous or current malignant tumors (except resected non-melanoma skin cancer and carcinoma in situ); 5. Patients suffering from NYHA Class III or IV heart failure, or with ECG showing QTc interval ≥ 550ms; 6. History of severe liver disease; 7. ALT or AST exceeded the upper limit of normal value by 2 times before inclusion; 8. Patients who had received immunosuppressive therapy within 3 months before enrollment; 9. Participated in other drug clinical trials within 3 months or medical device clinical trials within 1 month before admission; 10. Patients who are in the acute stage of thromboembolic disease; 11. Known blood clotting disorder or hemolysis; 12. Have uncontrolled chronic immune diseases (e.g. Rheumatoid arthritis, systemic lupus erythematosus, etc.); 13. Significant infection or C-reactive protein ≥ 30mg/L occurred; 14. Patients in the active stage of tuberculosis; 15. Pregnant and lactating women; 16. Patients with a history of gastrointestinal bleeding, massive bleeding or blood transfusion within 3 months before screening; 17. Serum ferritin < of subjects before enrollment; 100μg/L and transferrin saturation < 20%; 18. iPTH > of pre-enrolled subjects; 800pg/mL; 19. Persons who combine the use of aluminum preparations in the three months prior to screening, or who are engaged in work that may lead to the accumulation of aluminum in the body; 20. Patients who have a clear history of allergy to excipients of ESAs or rhEPO-Fc preparations, or who have been determined by the nvestigator to be potentially allergic to this product; 21. Patients who are taking antipsychotic drugs; 22. Life expectancy of less than 12 months; 23. Subjects determined by the investigator to be unsuitable candidates for the study (medical conditions that the investigator believes may pose a threat to the safety of subjects participating in the study, medical conditions that may confuse efficacy or safety evaluations, or medical conditions that may interfere with the subject's participation in the study). |
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研究实施时间: Study execute time: |
从 From 2020-02-02 00:00:00至 To 2023-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2021-06-16 00:00:00 至 To 2023-04-28 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: |
结束 /Completed |
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): |
在进行任何其他筛查程序前或终止任何不被允许的标准治疗前,必须获得知情同意。在签署书面知情同意后,研究中心将在交互式网络响应系统(IWRS)中登录受试者,并筛选受试者来评估是否符合参与研究的入选资格标准。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Informed consent must be obtained before any other screening procedure or before discontinuing any standard treatment that is not permitted. After signing the written informed consent, the Center will log in subjects in the Interactive Web Response System (IWRS) and screen subjects to assess whether they meet the eligibility criteria for participation in the study. |
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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: |
这是一项开放性研究。结合试验药和阳性对照药的给药方式(剂量和给药频率)以及试验操作过程,本试验研究中无法做到对患者、研究者的双盲。 在本次开放性的临床试验中,将通过设定研究者授权专门人员,在不知晓给药信息情况下对于安全性和疗效进行独立评价,来保证评价者盲。 |
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Blinding: |
This is an open study. Combined with the administration mode (dose and frequency) of the test drug and the positive control drug as well as the operation process of the trial, it is impossible to double-blind patients and investigators in this trial study. In this open clinical trial, evaluator blindness will be ensured by setting up investigator-authorized professionals to independently evaluate safety and efficacy without knowing the dosing information. |
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是否共享原始数据: IPD sharing |
否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): |
https://trial.cims-medtech.com/CIMS_V5/?uc=C037 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
https://trial.cims-medtech.com/CIMS_V5/?uc=C037 |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic Data Capture, EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |