A Study of MRG004A in Patients With Tissue Factor Positive Advanced or Metastatic Solid Tumors
2026年5月12日 更新者:Lepu Biopharma Co., Ltd.
An Open-Label, Multi-center, Phase I/II Dose Escalation and Expansion Study to Assess the Safety, Tolerability, Anti-Tumor Activity and Pharmacokinetics of MRG004A in Patients With Tissue Factor Positive Advanced or Metastatic Solid Tumors
The objective of this study is to evaluate the safety, efficacy, pharmacokinetics, and immunogenicity of MRG004A in patients with Tissue Factor positive advanced or metastatic solid tumors.
研究概览
详细说明
This study consists of two parts.
Part A is a dose escalation study to determine the maximum tolerated dose (MTD) and recommended phase II dose (RP2D) of MRG004A.
Part B is a disease specific multi-cohort dose expansion study to further assess the efficacy and safety of MRG004A at confirmed RP2D.
研究类型
介入性
注册 (实际的)
39
阶段
- 阶段2
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Hunan
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Changsha、Hunan、中国、410013
- Hunan Cancer Hospital
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、201321
- Fudan University Shanghai Cancer Center
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Zhejiang
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Hangzhou、Zhejiang、中国、310003
- The First Affiliated Hospital, College of Medicine, Zhejiang University
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California
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Orange、California、美国、92868-3201
- Chao Family Comprehensive Cancer Center
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New York
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New York、New York、美国、10065
- Memorial Sloan Kettering 60th Street Outpatient Center
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Ohio
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Canton、Ohio、美国、44718
- Gabrail Cancer Center Research
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Cincinnati、Ohio、美国、45219
- The Christ Hospital Cancer Center
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Pennsylvania
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Gettysburg、Pennsylvania、美国、17325
- Gettysburg Cancer Center
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Virginia
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Fairfax、Virginia、美国、22031
- Virginia Cancer Specialists
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
描述
Inclusion Criteria:
- Understands and provides written informed consent and willing to follow the requirements specified in protocol.
- Age ≥18 years.
- Life expectancy ≥6 months.
- For Part B patients, documented Tissue Factor (TF) presence in tumor biopsy specimens obtained from archival or re-biopsy specimens by immunohistochemistry (IHC) protein expression.
- Must have histologically or cytologically confirmed unresectable or metastatic cancer with documented disease progression during prior therapy, or relapse or progression following approved standard therapy for their tumor types- Part A and Part B.
- Part B: Patients who have documented progression during or relapse following standard therapy, no further treatment options that are known to improve survival, and participation in a clinical trial is a reasonable therapeutic option.
- Patients must have measurable disease per RECIST v1.1.
- ECOG performance status of 0 or 1.
- Acceptable bone marrow, hepatic, cardiac, renal, and coagulation function.
- A negative serum pregnancy test if female and aged between 18-55 years old.
- Patients, both females and males, of reproductive potential must agree to use adequate contraception during and for 180 days after the last infusion of MRG004A.
Exclusion Criteria:
- Archival or biopsy tumor shows TF IHC membrane or cytosolic score of zero, no TF-positive expression or no TF-positive staining in Part B patients.
- Toxicities (except alopecia & fatigue) due to prior antitumor therapy are greater than CTCAE v5.0 Grade 1.
- Toxicities due to prior radiotherapy that have not resolved to Grade ≤ 1 CTCAE v5.0 at least 21 days prior to the first treatment.
- Untreated, unstable or uncontrolled central nervous system (CNS) metastases.
- Any other type of anti-cancer therapy within 21 days of the first dose of study treatment. Use of any other type of anti-cancer treatment is prohibited throughout the study.
- Patients with increased bleeding risk.
- Presence of severe cardiac dysfunction.
- Pulmonary embolism or deep vein thrombosis within 3 months prior to the first dose of study drug.
- Concurrent malignancy within 5 years prior to entry.
- Uncontrolled or poorly controlled hypertension.
- History of ventricular tachycardia, or torsade des pointes.
- History of moderate to severe dyspnea at rest.
- Major surgery within 4 weeks of the first dose of study treatment and not fully recovered. Minor surgery within 2 weeks prior to study treatment.
- Known allergic reactions to any component or excipient of MRG004A or known allergic reactions to other prior anti-TF (including investigational) or other monoclonal antibody ≥ Grade 3.
- Patients who have any known liver disease, including chronic hepatitis B, hepatitis C, autoimmune hepatic disorders, primary biliary cirrhosis or sclerosing cholangitis; Patients who have concurrent, serious, uncontrolled infections or known infection with HIV, or have a diagnosed acquired immunodeficiency syndrome (AIDS); or an uncontrolled autoimmune disease, or have undergone organ transplant.
- Active uncontrolled bacterial, viral, fungal, rickettsial, or parasitic infection.
- Use of systemic corticosteroids within 4 weeks prior to the first dose of treatment.
- Use of strong CYP3A4 inhibitors or inducers with MRG004A.
- Other excluded medications or treatment: therapeutic anti-coagulative, or long-term anti-platelet treatment; multivitamins, calcium, vitamin D, and prophylactic anti-RANKL (denosumab) and zoledronic acid therapies for bone metastases are allowed.
- Any patient with a positive pregnancy or is breast-feeding.
- Any severe and/or uncontrolled systemic disease that at the discretion of investigator and sponsor makes it undesirable for the patient to participate in this study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:MRG004A
All patients in Part A (dose escalation) and Part B (dose expansion) will be administrated MRG004A on Day 1 of every 3 weeks (21-day cycle).
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Administrated intravenously
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Maximum Tolerated Dose (MTD)
大体时间:DLT will be evaluated during the first treatment cycle (Day 1-21)
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The highest dose confirmed wherein less than 2 out of 6, or < 33% of evaluable patients in a treatment cohort experiences dose-limiting toxicity (DLT).
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DLT will be evaluated during the first treatment cycle (Day 1-21)
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Recommended Phase II Dose (RP2D)
大体时间:Baseline to study completion (up to 24 months)
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The dose level of MRG004A recommended for further clinical studies based on assessment of the safety, efficacy and PK data from Part A of this study.
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Baseline to study completion (up to 24 months)
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Objective Response Rate (ORR)
大体时间:Baseline to study completion (up to 24 months)
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The proportion of patients who achieve complete response (CR) or partial response (PR) as assessed by the Independent Central Review (ICR).
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Baseline to study completion (up to 24 months)
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Adverse Events (AEs)
大体时间:From signing informed consent until 45 days after the last dose of MRG004A
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Any reaction, side effect, or untoward event that occurs during the course of the clinical trial whether or not the event is considered related to the study drug.
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From signing informed consent until 45 days after the last dose of MRG004A
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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响应持续时间(DOR)
大体时间:学习完成的基线(最多24个月)
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最早的合格反应日期与任何原因的疾病进展或死亡日期之间的时间间隔(以较早者为准)。
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学习完成的基线(最多24个月)
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Disease Control Rate (DCR)
大体时间:Baseline to study completion (up to 24 months)
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The proportion of patients who achieve CR, PR, or stable disease (SD) ≥ 6 weeks based on RECIST v1.1.
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Baseline to study completion (up to 24 months)
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Progression Free Survival (PFS)
大体时间:Baseline to study completion (up to 24 months)
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The time from the date of first study dose to disease progression or death whichever occurs first.
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Baseline to study completion (up to 24 months)
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Overall Survive (OS)
大体时间:Baseline to study completion (up to 24 months)
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The time from start of study treatment to date of death as a result of any cause.
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Baseline to study completion (up to 24 months)
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Pharmacokinetics (PK) Parameter of MRG004A: Cmax
大体时间:Baseline to 30 days after the last dose of study treatment
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Maximum observed plasma concentration.
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Baseline to 30 days after the last dose of study treatment
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Pharmacokinetics (PK) Parameter of MRG004A: Tmax
大体时间:Baseline to 30 days after the last dose of study treatment
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Time to reach the maximum plasma concentration.
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Baseline to 30 days after the last dose of study treatment
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Pharmacokinetics (PK) Parameter of MRG004A: AUClast
大体时间:Baseline to 30 days after the last dose of study treatment
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Area under the plasma concentration-time curve from time 0 to the time of last quantifiable concentration.
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Baseline to 30 days after the last dose of study treatment
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抗药抗体(ADA)发生率
大体时间:基线至最后一剂研究治疗药物后 30 天
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ADA 免疫原性结果阳性的患者比例。
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基线至最后一剂研究治疗药物后 30 天
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Nashat Y Gabrail, MD、Gabrail Cancer Center Research
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2021年7月26日
初级完成 (实际的)
2024年3月20日
研究完成 (实际的)
2024年7月26日
研究注册日期
首次提交
2021年4月8日
首先提交符合 QC 标准的
2021年4月11日
首次发布 (实际的)
2021年4月13日
研究记录更新
最后更新发布 (实际的)
2026年5月15日
上次提交的符合 QC 标准的更新
2026年5月12日
最后验证
2026年5月1日
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
是的
研究美国 FDA 监管的设备产品
不
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.