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A Phase III Study of SYHA1813 for Recurrent or Progressive High-Grade Meningiomas

SYHA1813 vs Investigators' Choice Treatment in Patients With Recurrent or Progressive High-Grade Meningiomas: A Randomized, Controlled, Multicenter, Phase III Study

This is a randomized, controlled, open-label, multicenter, Phase III clinical study designed to compare the efficacy and safety of SYHA1813 versus treatment of investigators' choice in patients with recurrent or progressive high-grade meningioma not amenable to local therapy.

研究概览

详细说明

Approximately136 participants with recurrent or progressive high-grade meningioma who have received surgical resection and radiotherapy will be enrolled and randomized 1:1 to receive either SYHA1813 (experimental group) or investigators' choice (control group) treatment. The primary endpoint is progression-free survival (PFS) assessed by blinded Independent Review Committee (BIRC) using the Response Assessment in Neuro-Oncology Working Group (RANO criteria) for meningioma.

研究类型

介入性

注册 (估计的)

136

阶段

  • 第三阶段

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:Clinical Trials Information Group Officer
  • 电话号码:86-0311-69085587
  • 邮箱ctr-contact@cspc.cn

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

描述

Inclusion Criteria:

  • 1. Aged >= 18 years.
  • 2. Histologically confirmed WHO grade II/III meningioma (WHO CNS 5th) that is progressive or recurrent.
  • 3. Individuals must have received surgery and radiation therapy.
  • 4. There is at least one measurable intracranial tumor lesion in the baseline period (RANO-meningioma).
  • 5. KPS≥60.
  • 6. The expected survival time is >=3 months.
  • 7. The organ function level and related laboratory indicators must meet requirement.
  • 8. Agree to use reliable and effective methods of contraception during the study treatment period and for at least 3 months after the last study treatment.

Exclusion Criteria:

  • 1. Individuals who are known to have severe allergic reaction to the study drug or any other ingredients/excipients in the formulation.
  • 2. Meets one of the following conditions: patients with brainstem involvement or extracranial metastasis; patients with severe brain herniation or at risk of brain herniation.
  • 3. History of other malignant tumors within 3 years or concurrent active malignant tumors.
  • 4. The toxic reactions of previous anti-tumor treatments have not yet recovered to ≤ Grade 1.
  • 5. Have used potent inhibitors or inducers of CYP3A4, CYP2C19 or CYP1A2 within the 14 days prior to randomization or are still requiring continued use of such agents.
  • 6. Individuals currently receiving warfarin or other oral anticoagulants (excluding those who use low-dose anticoagulants to maintain patency of central venous access or prevent deep vein thrombosis).
  • 7. Individuals who are unable to undergo enhanced MRI (such as those with pacemakers, metal dentures, claustrophobia, contrast agent allergies, etc.).
  • 8. Individuals with evidence or medical history of bleeding tendency within 2 months prior to randomization.
  • 9. Individuals with urine protein ≥ 2+, and 24-hour quantitative urine protein ≥ 1.0 g/24 h upon testing.
  • 10. History of acquired immunodeficiency syndrome or HIV antibody positivity in the past; Active hepatitis C; Active hepatitis B.
  • 11. Individuals with poorly healing wounds or ulcers, or fractures that require treatment or exhibit poor healing.
  • 12. Within 14 days prior to randomization, there were severe chronic or active infections (including tuberculosis infections) that required intravenous injection of antibacterial, antifungal or antiviral therapy.
  • 13. Individuals with cardiovascular and cerebrovascular diseases of significant clinical significance.
  • 14. Have undergone surgery of major vital organs within 28 days prior to randomization (excluding puncture biopsy).
  • 15. Individuals with swallowing difficulties or known medication absorption disorders.
  • 16. Pregnant or lactating women.
  • 17. Any other conditions that may interfere with the participant's adherence to study procedures, compromise the participant's best interests in participating in the study, or affect study results.

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:随机化
  • 介入模型:并行分配
  • 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:实验组
SYHA1813
SYHA1813 20mg QD
有源比较器:对照组
研究者选择的治疗
Investigator's Choice Treatment:bevacizumab, temozolomide or hydroxyurea

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Progression-Free Survival (PFS) as Assessed by RANO Criteria and Evaluated by BIRC
大体时间:Up to approximately 4 years
Up to approximately 4 years

次要结果测量

结果测量
大体时间
总生存期(OS)
大体时间:最长约 4 年
最长约 4 年
PFS as Assessed by RANO Criteria and Evaluated by investigators
大体时间:Up to approximately 4 years
Up to approximately 4 years
Overall Survival Rate at 12 Months (OS-12)
大体时间:Up to approximately 4 years
Up to approximately 4 years
Progression Free Survival Rate at 6 Months (PFS-6) as Assessed by RANO Criteria
大体时间:Up to approximately 4 years
Up to approximately 4 years
Objective Response Rate (ORR) as Assessed by RANO Criteria
大体时间:Up to approximately 4 years
Up to approximately 4 years
Disease Control Rate (DCR) as Assessed by RANO Criteria
大体时间:Up to approximately 4 years
Up to approximately 4 years
Frequency and severity of TEAEs and SAEs
大体时间:Up to approximately 4 years
Up to approximately 4 years
Cmax of SYHA1813
大体时间:Cycles 1, 2, 3
Cycles 1, 2, 3
Tmax of SYHA1813
大体时间:Cycles 1, 2, 3
Cycles 1, 2, 3
AUClast of SYHA1813
大体时间:Cycles 1, 2, 3
Cycles 1, 2, 3
AUCinf of SYHA1813
大体时间:Cycles 1, 2, 3
Cycles 1, 2, 3
t1/2 of SYHA1813
大体时间:Cycles 1, 2, 3
Cycles 1, 2, 3

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。

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5月20日

初级完成 (估计的)

2029年7月31日

研究完成 (估计的)

2029年10月15日

研究注册日期

首次提交

2026年5月18日

首先提交符合 QC 标准的

2026年5月21日

首次发布 (实际的)

2026年5月29日

研究记录更新

最后更新发布 (实际的)

2026年5月29日

上次提交的符合 QC 标准的更新

2026年5月21日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • SYHA1814-006

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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