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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: |
ChiCTR2400090997 |
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最近更新日期: Date of Last Refreshed on: |
2024-10-17 16:55:21 |
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注册时间: Date of Registration: |
2024-10-17 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: |
一项评估拓培非格司亭预防乳腺癌中高风险FN化疗方案导致的中性粒细胞减少疗效和安全性的多中心、前瞻性、观察性研究 |
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Public title: |
A Multicenter, Prospective, Observational Study to Evaluate the Efficacy and Safety of Telpegfilgrastim in Preventing Neutropenia Induced by Chemotherapy Regimens with High or Intermediate Risk of Febrile Neutropenia in Patients with Breast Cancer |
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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: |
一项评估拓培非格司亭预防乳腺癌中高风险FN化疗方案导致的中性粒细胞减少疗效和安全性的多中心、前瞻性、观察性研究 |
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Scientific title: |
A Multicenter, Prospective, Observational Study to Evaluate the Efficacy and Safety of Telpegfilgrastim in Preventing Neutropenia Induced by Chemotherapy Regimens with High or Intermediate Risk of Febrile Neutropenia in Patients with Breast Cancer |
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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: |
张少华 |
研究负责人: |
江泽飞 |
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Applicant: |
Zhang Shaohua |
Study leader: |
Jiang Zefei |
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申请注册联系人电话: Applicant telephone: |
+86 133 1159 1557 |
研究负责人电话: Study leader's telephone: |
+86 139 0137 2170 |
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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: |
zhangshaohua@csco.org.cn |
研究负责人电子邮件: Study leader's E-mail: |
jiangzefei@csco.org.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: |
北京市丰台区东大街8号 |
研究负责人通讯地址: |
北京市丰台区东大街8号 |
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Applicant address: |
8 Dongdajiedonglu,Fengtai District,Beijing Shi,China |
Study leader's address: |
8 Dongdajiedonglu,Fengtai District,Beijing Shi,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: |
中国人民解放军总医院第五医学中心 |
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Applicant's institution: |
Chinese People's Liberation Army (PLA)-307th Hospital |
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研究负责人所在单位: |
中国人民解放军总医院第五医学中心 |
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Affiliation of the Leader: |
Chinese People's Liberation Army (PLA)-307th Hospital |
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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: |
KY-2024-9-143-1 |
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: |
中国人民解放军总医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Chinese People's Liberation Army Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2024-09-30 00:00:00 |
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伦理委员会联系人: |
张昕洁 |
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Contact Name of the ethic committee: |
Zhang Xinjie |
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伦理委员会联系地址: |
北京市丰台区东大街8号 |
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Contact Address of the ethic committee: |
8 Dongdajiedonglu,Fengtai District,Beijing Shi,China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 6694 7798 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
ec307yy@163.com |
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研究实施负责(组长)单位: |
中国人民解放军总医院第五医学中心 |
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Primary sponsor: |
Chinese People's Liberation Army (PLA)-307th Hospital |
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研究实施负责(组长)单位地址: |
北京市丰台区东大街8号 |
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Primary sponsor's address: |
8 Dongdajiedonglu,Fengtai District,Beijing Shi,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: |
江苏复星医药销售有限公司 |
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Source(s) of funding: |
Jiangsu fosun pharmaceutical sales co. LTD |
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Target disease: |
neutropenia |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
针对接受中高风险FN化疗方案作为新辅助或辅助治疗的乳腺癌患者,评估拓培非格司亭预防化疗导致的中性粒细胞减少的有效性和安全性 |
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Objectives of Study: |
Evaluating the Efficacy and Safety of Telpegfilgrastim in Preventing Chemotherapy-Induced Neutropenia in Breast Cancer Patients Receiving Intermediate to High-Risk Chemotherapy as Neoadjuvant or Adjuvant Therapy. |
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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.经病理组织学或细胞学确诊为乳腺癌的患者,且经研究者评估适宜接受21d为1个周期含蒽环类和/或紫衫类化疗方案进行新辅助或辅助治疗,且后续至少接受≥2个化疗周期; 2.体重≥45kg; 3.年龄≥18岁且≤80岁; 4.ECOG评分≤2分; 5.血常规:血红蛋白≥90 g/L,白细胞计数≥4.0×10^9/L,血小板≥100×10^9/L,中性粒细胞≥2.0×10^9/L; 6.自愿参加本临床试验,理解并签署知情同意书。 |
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Inclusion criteria |
1. Patients with breast cancer confirmed by pathological histology or cytology, and deemed suitable by the investigator to receive a 21-day cycle containing anthracycline and/or taxane chemotherapy regimens for neoadjuvant or adjuvant therapy, and who will subsequently receive at least two cycles of chemotherapy; 2. Body weight ≥ 45 kg; 3. Age ≥ 18 years and ≤ 80 years; 4. ECOG score ≤ 2; 5. Routine blood test: Hemoglobin ≥ 90 g/L, white blood cell count ≥ 4.0 × 10^9/L, platelet count ≥ 100 × 10^9/L, neutrophil count ≥ 2.0 × 10^9/L; 6. Voluntarily participate in this clinical trial, understand and sign the informed consent form. |
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排除标准: |
1.筛选前2个月内或预期接受大面积放疗(>25%的骨髓总量); 2.无自知力或影响病情表述者; 3.未控制的感染或筛选前72小时内使用过抗生素者; 4.接受过或正在进行骨髓或器官移植者; 5.临床、心电图或者其它手段诊断为急性充血性心力衰竭、心肌病或者心肌梗塞; 6.伴有可能导致脾肿大的疾病; 7.药物或酒精滥用者; 8.已知对G-CSF或者药物的赋形剂过敏者; 9.筛选前1个月内使用其它研究药物或尚处于5个半衰期内(以时间长者为准); 10. 研究者认为患者存在不适合参加本研究的疾病或者症状,研究药物可能会损害患者健康或者会影响不良事件的判断。 |
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Exclusion criteria: |
1. Subjects had received or are anticipated to receive extensive radiotherapy (>25% of the total bone marrow volume) within 2 months prior to screening. 2. Lack of insight or ability to describe their medical condition; 3. Uncontrolled infection or use of antibiotics within 72 hours prior to screening; 4. History of or current bone marrow or organ transplantation; 5. Clinical, electrocardiographic, or other diagnostic evidence of acute congestive heart failure, cardiomyopathy, or myocardial infarction; 6. Presence of any disease that may lead to splenomegaly; 7. Substance or alcohol abusers; 8. Known hypersensitivity to G-CSF or excipients of the medication; 9. Use of other investigational drugs within 1 month prior to screening or still within 5 half-lives of the drug (whichever is longer); 10. Investigators believe that the patient has a disease or symptom that makes them unsuitable for this study, and the study medication may harm the patient's health or affect the judgment of adverse events. |
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研究实施时间: Study execute time: |
从 From 2024-08-10 00:00:00至 To 2026-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2024-10-18 00:00:00 至 To 2025-10-31 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: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
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性别: |
女性 |
Gender: |
Female |
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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): |
None |
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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): |
不适用 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Not apply |
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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: |
EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |