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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: |
ChiCTR2600117450 |
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最近更新日期: Date of Last Refreshed on: |
2026-01-23 17:40:14 |
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注册时间: Date of Registration: |
2026-01-23 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: |
罗普司亭N01治疗肿瘤治疗所致血小板减少症 |
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Public title: |
Romiplostim N01 for the treatment of cancer treatment-induced thrombocytopenia |
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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: |
罗普司亭N01治疗肿瘤治疗所致血小板减少症的有效性和安全性多中心、前瞻性、非随机对照研究 |
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Scientific title: |
A multi-center, prospective, single-arm study on the efficacy and safety of romiplostim N01 in the cancer treatment-induced thrombocytopenia caused by tumor treatment |
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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: |
王朋 |
研究负责人: |
王朋 |
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Applicant: |
Peng Wang |
Study leader: |
Peng Wang |
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申请注册联系人电话: Applicant telephone: |
+86 13562677025 |
研究负责人电话:
Study leader's |
+86 536 33567663 |
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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: |
wangpeng1920@sohu.com |
研究负责人电子邮件: Study leader's E-mail: |
wangpeng1920@sohu.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: |
山东省青州市将军山路5158号 |
研究负责人通讯地址: |
山东省青州市将军山路5168号 |
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Applicant address: |
No. 5158, Jiangjunshan Road, Qingzhou City, Shandong Province |
Study leader's address: |
No 5168 Jiangjunshan Road Qingzhou City Shandong Province |
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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: |
潍坊市益都中心医院 |
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Applicant's institution: |
Yidu Central Hospital of Weifang City |
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研究负责人所在单位: |
潍坊市益都中心医院 |
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Affiliation of the Leader: |
Yidu Central Hospital of Weifang City |
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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: |
KYLLSC2025003;KYLLSC2025003-02 |
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: |
潍坊市益都中心医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Weifang Yidu Central Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-07-11 00:00:00 | ||
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伦理委员会联系人: |
赵静 |
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Contact Name of the ethic committee: |
Zhao Jing |
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伦理委员会联系地址: |
山东省青州市将军山路5168号 |
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Contact Address of the ethic committee: |
No 5168 Jiangjunshan Road Qingzhou City Shandong Province |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 536 3567988 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
yiwuchu3275532@163.com |
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研究实施负责(组长)单位: |
潍坊市益都中心医院 |
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Primary sponsor: |
Yidu Central Hospital of Weifang City |
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研究实施负责(组长)单位地址: |
山东省青州市将军山路5168号 |
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Primary sponsor's address: |
No 5168 Jiangjunshan Road Qingzhou City Shandong Province |
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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: |
自选课题(自筹) |
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Source(s) of funding: |
Self-selected topic |
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研究疾病: |
肿瘤治疗所致血小板减少症 |
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Target disease: |
cancer treatment-induced thrombocytopenia |
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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: |
其它 | ||||||||||||||||||||||
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Study phase: |
N/A |
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研究设计: |
非随机对照试验 |
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Study design: |
Non randomized control |
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研究目的: |
评估罗普司亭N01治疗及预防肿瘤治疗所致血小板减少症的有效性 |
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Objectives of Study: |
Evaluate the efficacy of romiplostim N01 in the treatment and prevention of cancer treatment-induced thrombocytopenia |
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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.年龄18-75周岁(含),性别不限; 2.经组织或病理证实的实体瘤或血液肿瘤; 3.经确诊的因抗肿瘤治疗导致的血小板减少症患者,4级、3级及2级治疗不佳(应用常规升板治疗效果连用5天效果不佳[效果不佳:较基线上升不足30%])的患者; 4.ECOG PS评分0-2分; 5.预计生存期≥12周;且预计可以接受当前抗肿瘤治疗方案(化疗或 ADC 药物,可以联合靶向及免疫)治疗≥1 个周期; 6.育龄期受试者,同意在整个研究期间采取可靠的避孕措施;已接受子宫切除术、双侧输卵管切除术、双侧输卵管结扎术或绝经后超过1 年的女性受试者及双侧输精管切除术或结扎术的男性受试者除外; 7.自愿参加研究并签署知情同意书,能够遵守临床试验的各种要求(计划内访视和其他试验程序等); 8.研究者判断的可以入组的受试者; |
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Inclusion criteria |
1.Aged between 18 and 75 (inclusive), gender is not restricted; 2.Histologically or pathologically confirmed solid tumors or hematological malignancies; 3.Patients with confirmed thrombocytopenia caused by anti-tumor treatment, including those with grade 4, grade 3, and grade 2 whose treatment is ineffective (the effect of conventional platelet-raising treatment is ineffective after 5 consecutive days of use [ineffective: the increase compared to the baseline is less than 30%]); 4.ECOG 0-2; 5.Expected survival >=12 weeks; and expected to be able to receive the current anti-tumor treatment regimen (chemotherapy or ADC drugs, which can be combined with targeted therapy and immunotherapy) for >=1 cycle. 6.Subjects of childbearing age should agree to take reliable contraceptive measures throughout the study period; female subjects who have undergone hysterectomy, bilateral salpingectomy, bilateral tubal ligation or have been post - menopausal for more than 1 year and male subjects who have undergone bilateral vasectomy or ligation are excluded; 7.Voluntarily participate in the research and sign the informed consent form, and be able to comply with various requirements of the clinical trial (such as scheduled visits and other trial procedures); 8.Subjects judged by the researcher to be eligible for enrollment; |
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排除标准: |
6个月内新发动脉或深静脉血栓史的受试者; |
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Exclusion criteria: |
1.Subjects with a history of newly developed arterial or deep vein thrombosis within 6 months; 2.Screen for cases of thrombocytopenia caused by reasons other than chemotherapy drugs within the previous six months, including but not limited to chronic liver disease, hypersplenism, and infection; 3.Suffering from hematopoietic system diseases, including but not limited to aplastic anemia, leukemia, primary immune thrombocytopenia, myelodysplastic syndrome, multiple myeloma, etc; 4.Require urgent treatment, such as vena cava syndrome and spinal cord compression syndrome; 5.Abnormal liver function, defined as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 3 times the upper limit of the normal reference range (in patients without liver metastases) or 5 times (in patients with liver metastases); 6.Renal function abnormality, defined as serum creatinine ≥ 1.5 times the upper limit of the normal reference range or eGFR <= 60 ml/min; 7.Screen patients who received romiplostim treatment within the previous month; 8.Received platelet transfusion therapy within 1 week before enrollment; 9.Pregnant or lactating women; 10.Those who are allergic to the test drug or its ingredients; 11.Subjects who participated in other drug clinical trials or interventional studies within the past month; 12.Other conditions judged by the researcher as unsuitable for enrollment in this study; |
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研究实施时间: Study execute time: |
从 From 2025-07-30 00:00:00至 To 2027-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2026-01-23 00:00:00 至 To 2027-04-30 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): |
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: |
无 |
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Blinding: |
None |
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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): |
在试验结束后,研究者有权发表或发布本临床试验自己承担的部分病例的研究结果,但在发表或发布之前,应征得申办者的书面同意,且未经申办者同意,不得私自发表论文。 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
At the conclusion of the trial, the investigator has the right to publish or present research results based on the portion of clinical trial cases for which they are responsible. However, prior to publication or presentation, written consent must be obtained from the sponsor. Research papers may not be published without the sponsor's approval. |
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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: |
病历记录表、电子采集和病历系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Report Form, Electronic Data Capture (EDC), and the medical record system. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |