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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: |
ChiCTR2500110587 |
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最近更新日期: Date of Last Refreshed on: |
2025-10-16 09:28:51 |
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注册时间: Date of Registration: |
2025-10-16 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: |
注射用QLC5508联合用药治疗在晚期实体瘤患者中的安全性、耐受性、药代动力学和有效性的开放、多中心Ib/II期临床研究 |
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Public title: |
An open-label, multicenter Phase Ib/II clinical study on the safety, tolerability, pharmacokinetics, and efficacy of QLC5508 injection combined therapy in patients with advanced solid tumors |
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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: |
注射用QLC5508联合用药治疗在晚期实体瘤患者中的安全性、耐受性、药代动力学和有效性的开放、多中心Ib/II期临床研究 |
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Scientific title: |
An open-label, multicenter Phase Ib/II clinical study on the safety, tolerability, pharmacokinetics, and efficacy of QLC5508 injection combined therapy in patients with advanced solid tumors |
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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: |
刘倩芸 |
研究负责人: |
周彩存 |
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Applicant: |
Qianyun Liu |
Study leader: |
Caicun Zhou |
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申请注册联系人电话: Applicant telephone: |
+86 531 5582 1177 |
研究负责人电话:
Study leader's |
+86 21 5882 2171 |
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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: |
qianyun.liu@qilu-pharma.com |
研究负责人电子邮件: Study leader's E-mail: |
caicunzhoudr@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: |
山东省济南市历城区旅游路8888号 |
研究负责人通讯地址: |
上海市浦东新区云台路1800号 |
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Applicant address: |
8888 Lvyou Road, Licheng District, Jinan, Shandong, China |
Study leader's address: |
150 Jimo Road, Pudong New District, Shanghai, 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: |
齐鲁制药有限公司 |
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Applicant's institution: |
Qilu Pharmaceutical Co. |
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研究负责人所在单位: |
上海市东方医院 |
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Affiliation of the Leader: |
Shanghai East 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: |
[2025]临审(073)号 |
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: |
上海市东方医院药物/器械临床试验伦理委员会 |
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Name of the ethic committee: |
Shanghai East Hospital Medical Ethics Committee (Drug/Device Clinical Trial) |
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伦理委员会批准日期: Date of approved by ethic committee: |
2025-08-05 00:00:00 | ||
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伦理委员会联系人: |
鲍思蔚 |
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Contact Name of the ethic committee: |
Siwei Bao |
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伦理委员会联系地址: |
上海市浦东新区云台路1800号 |
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Contact Address of the ethic committee: |
1800 Yuntai Road, Pudong New Area, Shanghai, China |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 21 3880 4518 |
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: |
上海市东方医院 |
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Primary sponsor: |
Shanghai East Hospital |
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研究实施负责(组长)单位地址: |
上海市浦东新区云台路1800号 |
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Primary sponsor's address: |
1800 Yuntai Road, Pudong New Area, Shanghai, 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: |
齐鲁制药有限公司 |
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Source(s) of funding: |
Qilu Pharmaceutical Co. |
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研究疾病: |
晚期实体瘤 |
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Target disease: |
Advanced Solid Tumor |
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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: |
I期+II期 | ||||||||||||||||||||||
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Study phase: |
1-2 |
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研究设计: |
单臂 |
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Study design: |
Single arm |
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研究目的: |
评价QLC5508各联合治疗方案在晚期实体瘤患者中的安全性和耐受性。 |
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Objectives of Study: |
The objectives of this study are to investigate the safety, tolerability, pharmacokinetics, and antitumor activity of QLC5508 in combination with other anticancer agents in patients with advanced solid tumors. |
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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.肿瘤诊断和既往抗肿瘤治疗史; 2.年满18周岁(≥18周岁)的男性或女性; 3.根据RECIST 1.1,受试者至少有1个靶病灶; 4.美国东部肿瘤协作组(ECOG)体力状况评分(PS)为0~1分; 5.最小预期生存大于12周; 6.具有生育能力的女性患者愿意在从签署知情同意起到末次给药或终止治疗后6个月内采取合适的避孕措施; 7.女性患者在首次给药前7天内,血妊娠试验结果为阴性; 8.自愿参加本次临床试验,理解研究程序且能够书面签署知情同意书。 |
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Inclusion criteria |
1.Tumor diagnosis and history of prior anti-tumor therapy; 2.At least 18 years of age at screening; 3.At least one measurable target lesion according to RECIST v1.1; 4.Eastern Cooperative Oncology Group (ECOG) Performance Status of 0~1; 5.Life expectancy >=12 weeks; 6.Female or male participants should be willing to use appropriate contraceptive measures throughout the study; 7. Female participants should have a negative blood pregnancy test within 7 days prior to the first dose or have evidence of non-childbearing potential; 8. A signed written Informed Consent Form. |
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排除标准: |
1.既往接受过或正在进行B7-H3为靶点、拓扑异构酶I抑制物类药物的治疗; 2.存在既往治疗遗留的按不良事件常用术语标准(CTCAE 5.0版)≥2级的毒性; 3.其他原发性实体瘤病史; 4.骨髓储备或肝肾器官功能不足; 5.严重的心脏疾病; 6.有严重、未控制的系统性疾病; 7.首次给药前4周内发生过严重感染或筛选期存在为控制的活动性感染; 8.已知或可疑有间质性肺炎; 9.存在消化道出血或腹腔出血的高风险; 10.首次给药前3 个月内有临床意义的消化道疾病; 11.既往有严重的神经或精神障碍史; 12.经研究者判断可能对研究的程序和要求依从性不佳的患者; 13.经研究者判断存在任何危及患者安全或干扰研究评估的状况的患者。 |
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Exclusion criteria: |
1.Previous or current treatment with B7-H3-targeted investigational therapy or topoisomerase I inhibitors; 2.Unresolved AEs ≥ Grade 2 (CTCAE v5.0) from prior therapy except for alopecia and residual neuropathy; 3.Previous or concurrent primary malignancies; 4.Inadequate bone marrow reserve or organ dysfunction; 5.Evidence of cardiovascular risk; 6.Evidence of current severe or uncontrolled systemic diseases; 7.Severe infection within 4 weeks prior to the first dose; or uncontrolled active infection at screening; 8.Known or suspected interstitial lung disease; 9.High risk of gastrointestinal or abdominal bleeding; 10.Gastrointestinal diseases of clinical significance within 3 months prior to the first dose; 11.History of severe neuropathy or mental disorders; 12.Unlikely to comply with study procedures and requirements in the opinion of the investigator; 13. Any disease or condition that, in the opinion of the investigator, would compromise participant safety or interfere with study assessments; |
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研究实施时间: Study execute time: |
从 From 2025-08-01 00:00:00至 To 2028-06-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2025-10-24 00:00:00 至 To 2026-10-31 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: |
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: |
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Blinding: |
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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: |
研究医生根据受试者的原始观察记录,将数据及时、完整、正确、清晰地载入病例报告表。经过监查员审核、签字后的调查表应及时送交临床研究数据管理员。 当所有病例报告表输入并核对无误后,由数据管理员写出数据库检查报告,其内容包括研究完成情况(含脱落受试者清单)、入选/排除标准检查、完整性检查、逻辑一致性检查、离群数据检查、时间窗检查、合并用药检查、不良事件检查等。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The study investigator shall transcribe the data from the subject's original observations into the case report form (CRF) in a timely, complete, accurate, and legible manner. The CRFs, after being reviewed and signed by the monitor, should be promptly submitted to the clinical data manager. After all CRFs have been entered and verified, the data manager shall generate a database audit report. This report shall include, but not be limited to, the following: study completion status (including a list of screen failures and discontinued subjects), checks against inclusion/exclusion criteria, completeness checks, logical consistency checks, outlier checks, time window checks, concomitant medication checks, and adverse event checks. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |