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IN10018 in Combination With Dalpiciclib for Progressive Meningiomas

2026年8月5日 更新者:Hongwei Zhang、Capital Medical University

An Open-Label Phase Ib Clinical Study Evaluating the Safety, Tolerability, and Efficacy of IN10018 in Combination With Dalpiciclib in Participants With Progressive Meningiomas

This open-label Phase Ib study will evaluate the safety, tolerability, and preliminary effectiveness of IN10018 in combination with dalpiciclib in adults with progressive meningiomas. Progressive meningiomas are tumors arising from the membranes surrounding the brain that have continued to grow or have returned after previous treatment.

Participants will receive both study drugs by mouth in 28-day treatment cycles. IN10018 will be taken once daily throughout each cycle, and dalpiciclib will be taken once daily for 21 days followed by 7 days without dalpiciclib. Treatment may continue until the tumor progresses, unacceptable side effects occur, or another reason for stopping treatment applies.

The study includes a dose-confirmation phase and a dose-expansion phase. The main goals are to evaluate side effects and determine a recommended dose of the combination for further study. Researchers will also assess whether the treatment can shrink tumors or delay tumor growth, measure how the drugs are processed in the body, and explore tumor and blood biomarkers that may be associated with treatment response.

研究概览

研究类型

介入性

注册 (估计的)

24

阶段

  • 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。

学习联系方式

  • 姓名:Research Secretary
  • 电话号码:+86 18701200112
  • 邮箱:503071697@qq.com

学习地点

      • Beijing、中国
        • 尚未招聘
        • Sanbo Brain Hospital, Capital Medical University
    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100093
        • 招聘中
        • Beijing Sanbo Brain Hospital, Capital Medical University
        • 接触:

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

Inclusion Criteria:

Participants must be able to understand and willing to sign a written informed consent form and agree to comply with all study requirements. Written informed consent must be obtained before any study-related examination or procedure is performed.

Aged 18 years or older, male or female.

Histologically confirmed meningioma meeting at least one of the following conditions:

  1. World Health Organization (WHO) Grade 2 or Grade 3 meningioma; or
  2. WHO Grade 1 meningioma that has recurred after surgery or radiotherapy and demonstrates clear radiographic or clinical progression, as determined by the investigator.

No available standard treatment option, or failure of standard treatment, including surgery, radiotherapy, or other systemic therapy.

At least 24 weeks must have elapsed since completion of radiotherapy, including external beam radiation therapy, brachytherapy, or radiosurgery such as Gamma Knife or CyberKnife.

At least one measurable lesion according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1), as confirmed by the investigator.

Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2. Estimated life expectancy of at least 3 months, as determined by the investigator.

Adverse effects caused by previous treatments must have recovered to Grade 1 or lower according to the Common Terminology Criteria for Adverse Events (CTCAE), except for alopecia and fatigue.

The dose of corticosteroids or other hormonal treatment must have been stable for at least 4 days before enrollment.

Adequate hematologic and organ function, based on laboratory tests performed within 7 days before the first dose, as follows:

Hematologic function:

  1. Hemoglobin of at least 100 g/L, without dependence on red blood cell transfusion or erythropoietin.
  2. Platelet count of at least 100 × 10^9/L, without dependence on platelet transfusion.
  3. Absolute neutrophil count of at least 1.5 × 10^9/L, without the use of colony-stimulating factors.

    Hepatic function:

  4. Total bilirubin no greater than the upper limit of normal.
  5. Alanine aminotransferase and aspartate aminotransferase no greater than 2.5 times the upper limit of normal.

    Renal function:

  6. Serum creatinine no greater than 1.5 times the upper limit of normal.
  7. Either creatinine clearance calculated using the Cockcroft-Gault formula of at least 60 mL/min or estimated glomerular filtration rate calculated using the Modification of Diet in Renal Disease formula of at least 60 mL/min/1.73 m².

    Urinary protein and coagulation function:

  8. Urine protein negative or trace. Participants with urine protein of 1+ must have a morning spot urine protein-to-creatinine ratio of less than 0.5 or 24-hour urinary protein of less than 0.5 g/24 hours.
  9. International normalized ratio no greater than 1.5 and activated partial thromboplastin time no greater than 1.5 times the upper limit of normal.

Female participants must not be pregnant or breastfeeding and must meet one of the following conditions:

  1. Not be a woman of childbearing potential; or
  2. If a woman of childbearing potential, agree to follow the protocol-specified contraceptive requirements during study treatment and for 3 months after the last dose.

Exclusion Criteria:

Major surgery or major trauma within 28 days before the first dose, or diagnostic biopsy within 14 days before the first dose.

Receipt of systemic anticancer treatment, including an investigational drug, within the protocol-specified washout period, including chemotherapy or targeted therapy within 14 days or 5 half-lives before the first dose, whichever is shorter, or immunotherapy within 28 days before the first dose.

Previous treatment with a focal adhesion kinase inhibitor or a cyclin-dependent kinase 4/6 inhibitor, including dalpiciclib.

A serious cardiovascular event or clinically significant cardiovascular condition within 6 months before initiation of study treatment, including but not limited to:

  1. Left ventricular ejection fraction below 50%;
  2. Corrected QT interval greater than 480 milliseconds;
  3. New York Heart Association functional class 2 or higher;
  4. History of serious arrhythmia or cardiomyopathy. Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage. Participants with small-volume effusions detectable only by imaging may be considered eligible.

Malabsorption syndrome or inability to take oral medication. Serious gastrointestinal disease, including uncontrolled inflammatory gastrointestinal disease, active Crohn disease, active ulcerative colitis, or uncontrolled gastrointestinal bleeding.

Active infection that is not adequately controlled by systemic treatment. Known human immunodeficiency virus infection. Human immunodeficiency virus testing is not required during screening unless mandated by local regulations or institutional policy.

Known active hepatitis B virus or hepatitis C virus infection. Hepatitis B virus and hepatitis C virus testing is not required during screening unless mandated by local regulations or institutional policy.

Any medical history, treatment, laboratory abnormality, or other condition that, in the investigator's judgment, could confound interpretation of the study results, interfere with participant compliance, or compromise the participant's safety or interests.

Known psychiatric illness or substance abuse that could interfere with compliance with study requirements.

Known hypersensitivity to IN10018, dalpiciclib, or any component of either study drug.

Systemic treatment with a strong inhibitor or inducer of CYP3A4, CYP2D6, or P-glycoprotein within 14 days before the first dose, or anticipated need for such treatment during the study treatment period.

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
实验性的:IN10018 Plus Dalpiciclib
Participants will receive oral IN10018 in combination with oral dalpiciclib in 28-day treatment cycles. IN10018 will be administered once daily continuously at 100 mg, with a permitted reduced dose of 50 mg. Dalpiciclib will be administered once daily at 125 mg on Days 1 through 21 of each cycle, followed by 7 days off treatment, with a permitted reduced dose of 100 mg. A modified 3+3 design will be used during dose confirmation to determine the recommended dose. Participants enrolled in the dose-expansion phase will receive the combination at the recommended dose. Treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined discontinuation criterion.
Ifebemtinib (IN10018) is an investigational oral focal adhesion kinase inhibitor. It will be administered once daily continuously during each 28-day treatment cycle. The starting dose is 100 mg once daily. If the starting dose is not tolerated, the dose may be reduced to 50 mg once daily. Ifebemtinib will be administered in combination with dalpiciclib until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined discontinuation criterion.
Dalpiciclib is an oral, selective cyclin-dependent kinase 4 and 6 inhibitor. It will be administered at a starting dose of 125 mg once daily on Days 1 through 21 of each 28-day treatment cycle, followed by 7 days without dalpiciclib. If the starting dose is not tolerated, the dose may be reduced to 100 mg once daily. Dalpiciclib will be administered in combination with ifebemtinib until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined discontinuation criterion.

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
Incidence of Dose-Limiting Toxicities (DLTs)
大体时间:Dose-limiting toxicities will be assessed at the end of Cycle 1 (each cycle is 28 days).
The number and percentage of participants who experience at least one protocol-defined dose-limiting toxicity during Cycle 1. Dose-limiting toxicities will be assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0, and must be considered related to IN10018 and/or dalpiciclib.
Dose-limiting toxicities will be assessed at the end of Cycle 1 (each cycle is 28 days).
Incidence of Treatment-Emergent Adverse Events
大体时间:Adverse events will be assessed from the first dose through 30 days after the last dose of study treatment, up to approximately 24 months.
Number and percentage of participants who experience treatment-emergent adverse events, treatment-related adverse events, serious adverse events, Grade 3 or higher adverse events, or adverse events resulting in treatment interruption, dose reduction, or permanent treatment discontinuation. Adverse events will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE), version 5.0.
Adverse events will be assessed from the first dose through 30 days after the last dose of study treatment, up to approximately 24 months.

次要结果测量

结果测量
措施说明
大体时间
Objective Response Rate (ORR)
大体时间:From first dose until disease progression, initiation of new anticancer therapy, withdrawal, death, or study completion, up to 36 months.
Percentage of participants with a best overall response of complete response or partial response according to RANO for Meningioma.
From first dose until disease progression, initiation of new anticancer therapy, withdrawal, death, or study completion, up to 36 months.
Six-Month Progression-Free Survival Rate (PFS-6)
大体时间:At 6 months after the first dose.
Percentage of participants alive without radiographic disease progression at 6 months after the first dose of study treatment.
At 6 months after the first dose.
Disease Control Rate (DCR)
大体时间:From first dose until disease progression, withdrawal, death, or study completion, up to 36 months.
Percentage of participants achieving CR, PR, minor response (MR), or stable disease (SD) lasting at least 8 weeks.
From first dose until disease progression, withdrawal, death, or study completion, up to 36 months.
Duration of Response (DoR)
大体时间:From first documented response until disease progression or death, up to 36 months.
Time from the first documented objective response (CR or PR) until disease progression or death from any cause.
From first documented response until disease progression or death, up to 36 months.
Progression-Free Survival (PFS)
大体时间:From first dose until disease progression or death, up to 36 months.
Time from the first dose of study treatment until radiographic disease progression according to RANO criteria or death from any cause.
From first dose until disease progression or death, up to 36 months.
Overall Survival (OS)
大体时间:From first dose until death from any cause, up to 36 months.
Time from the first dose of study treatment until death from any cause.
From first dose until death from any cause, up to 36 months.

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:Hongwei Zhang, MD, PhD、Beijing Sanbo Brain Hospital, Capital Medical University

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 (估计的)

2026年8月1日

初级完成 (估计的)

2028年8月1日

研究完成 (估计的)

2029年8月1日

研究注册日期

首次提交

2026年6月5日

首先提交符合 QC 标准的

2026年6月11日

首次发布 (实际的)

2026年6月17日

研究记录更新

最后更新发布 (实际的)

2026年8月7日

上次提交的符合 QC 标准的更新

2026年8月5日

最后验证

2026年8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

不

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.

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