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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: |
ChiCTR2500110467 |
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最近更新日期: Date of Last Refreshed on: |
2025-10-14 15:47:16 |
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注册时间: Date of Registration: |
2025-10-14 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: |
氟泽雷塞治疗晚期KRAS G12C突变NSCLC疗效和安全性评估,一项多中心、非干预、观察性研究(IBI351-RWS-001) |
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Public title: |
Efficacy and Safety Evaluation of Fulzerasib in the Treatment of Advanced NSCLC with KRAS G12C Mutation: A Multicenter, Non-Interventional, Observational Study (IBI351-RWS-001) |
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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: |
氟泽雷塞治疗晚期KRAS G12C突变NSCLC疗效和安全性评估,一项多中心、非干预、观察性研究(IBI351-RWS-001) |
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Scientific title: |
Efficacy and Safety Evaluation of Fulzerasib in the Treatment of Advanced NSCLC with KRAS G12C Mutation: A Multicenter, Non-Interventional, Observational Study (IBI351-RWS-001) |
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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: |
王燕 |
研究负责人: |
王燕 |
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Applicant: |
Wang Yan |
Study leader: |
Wang Yan |
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申请注册联系人电话: Applicant telephone: |
+86 10 87787471 |
研究负责人电话:
Study leader's |
+86 10 87787471 |
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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: |
wangyanyifu@163.com |
研究负责人电子邮件: Study leader's E-mail: |
wangyanyifu@163.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: |
北京市朝阳区潘家园南里17号院 |
研究负责人通讯地址: |
北京市朝阳区潘家园南里17号 |
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Applicant address: |
No. 17, South Panjiayuan, Chaoyang District, Beijing |
Study leader's address: |
No. 17, South Panjiayuan, Chaoyang District, Beijing |
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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: |
中国医学科学院肿瘤医院 |
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Applicant's institution: |
Cancer Hospital Chinese Academy of Medical Science |
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研究负责人所在单位: |
中国医学科学院肿瘤医院 |
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Affiliation of the Leader: |
Cancer Hospital Chinese Academy of Medical Sciences |
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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: |
25/119-5065 |
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: |
中国医学科学院肿瘤医院伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of Chinese Academy of Medical Sciences and Peking Union Medical College |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-03-27 00:00:00 | ||
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伦理委员会联系人: |
吴大维 |
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Contact Name of the ethic committee: |
Wu Dawei |
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伦理委员会联系地址: |
北京市朝阳区潘家园南里17号院 |
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Contact Address of the ethic committee: |
No. 17, South Panjiayuan, Chaoyang District, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 87788495 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
wumingshi-117@163.com |
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研究实施负责(组长)单位: |
中国医学科学院肿瘤医院 |
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Primary sponsor: |
Cancer Hospital Chinese Academy of Medical Sciences |
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研究实施负责(组长)单位地址: |
北京市朝阳区潘家园南里17号院 |
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Primary sponsor's address: |
No. 17, South Panjiayuan, Chaoyang 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: |
信达生物制药(苏州)有限公司 |
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Source(s) of funding: |
Innovent Biologics (Suzhou) Co. Ltd. |
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研究疾病: |
晚期KRASG12C突变NSCLC |
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Target disease: |
Advanced NSCLC with KRAS-G12C mutation |
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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: |
观察性研究 |
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Study type: |
Observational 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: |
连续入组 |
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Study design: |
Sequential |
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研究目的: |
氟泽雷塞在真实世界中使用的治疗模式及有效性和安全性评估 |
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Objectives of Study: |
Evaluation of Treatment Patterns, Efficacy and Safety of Fluzoparib in Real-World |
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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.病理确认为NSCLC; 2. 根据国际肺癌研究协会和美国癌症分类联合委员会第9版肺癌TNM分期,具有组织学或细胞学证实的不能手术切除且不能接受根治性同步放化疗的局部晚期(III B/ III C期)、转移性或复发性(IV期)NSCLC受试者; 3. 分子检测确定KRAS G12C突变; 4. 经研究者评估拟接受氟泽雷塞治疗。 |
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Inclusion criteria |
1. NSCLC confirmed by pathology; 2. Patients with histologically or cytologically confirmed locally advanced (stage IIIB/IIIC), metastatic or recurrent (stage IV) NSCLC according to the International Association for the Study of Lung Cancer and American Joint Committee on Classification of Cancer 9th Edition TNM staging system for lung cancer, who are inoperable for surgical resection and cannot receive definitive concurrent chemoradiotherapy; 3.KRAS G12C mutation was identified by molecular analysis; 4. Intention to receive fluzeresel, as assessed by the investigator. |
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排除标准: |
1.标准治疗有效的驱动基因阳性患者包括但不限于EGFR/MET/ROS1/ALK等,尚未进行标准治疗,或标准治疗后尚未进展。 2. 妊娠或哺乳的女性患者。 3. 未控制的并发性疾病,研究者评估不接受靶向治疗的患者,包括但不限于: 1) HIV 感染者(HIV抗体阳性)。 2)处于活动期或临床控制不佳的严重感染。 3)存在严重或不能控制的全身性疾病(如严重的精神、神经疾病、癫痫或痴呆,不稳定或不能代偿的呼吸、心血管、肝或肾脏疾病,未得到控制的高血压[即指经过药物治疗后仍为大于或等于CTCAE 2级高血压])的证据。 4)有活动性出血或新发血栓性疾病正在服用治疗量抗凝药物或有出血倾向者。 |
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Exclusion criteria: |
1. Driver gene positive patients who responded to standard therapy, including but not limited to EGFR/MET/ROS1/ALK, have not received standard therapy, or have not progressed after standard therapy. 2. Pregnant or lactating women. 3. Uncontrolled co-morbidity, as assessed by investigators in patients not receiving targeted therapy, including but not limited to: 1) patients with HIV infection (HIV antibody positive). 2) severe infections that are active or poorly controlled clinically. 3) evidence of severe or uncontrolled systemic illness (e.g., severe psychiatric, neurological illness, epilepsy, or dementia, unstable or decompensated respiratory, cardiovascular, hepatic, or renal disease, uncontrolled hypertension [i.e., hypertension greater than or equal to CTCAE class 2 despite medical treatment]). 4) patients with active bleeding, new thrombotic disease taking therapeutic dose of anticoagulant drugs, or bleeding tendency. |
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研究实施时间: Study execute time: |
从 From 2025-01-30 00:00:00至 To 2027-11-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-10-16 00:00:00 至 To 2026-12-30 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 |
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): |
无 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
None |
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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;EDC |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
CRF;EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |