TGF-β受体抑制剂Galunisertib (LY2157299)和Enzalutamide在转移性去势抵抗性前列腺癌中的研究
使用 TGF-β 受体抑制剂 LY2157299 和恩杂鲁胺的新型组合克服转移性去势抵抗性前列腺癌的耐药性:一项随机多中心 II 期研究
The primary objective of this study is to compare the progression free survival (PFS) of patients with metastatic castration-resistant prostate cancer treated with enzalutamide in combination with LY2157299 (Arm 1) versus enzalutamide alone (Arm 2).
研究概览
研究类型
注册 (实际的)
阶段
- 阶段2
联系人和位置
学习地点
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District of Columbia
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Washington D.C.、District of Columbia、美国、20016
- Sibley Memorial Hospital
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Illinois
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Chicago、Illinois、美国、60611
- Northwestern University
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Chicago、Illinois、美国、60637
- University of Chicago
-
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Maryland
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Baltimore、Maryland、美国、21205
- Johns Hopkins University
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Have metastatic castration-resistant prostate cancer
- Must have had prior abiraterone treatment
- Life expectancy of greater than 3 months
- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 2
- Age ≥18 years
- Have measurable disease
- Patients acceptance to have a tumor biopsy of an accessible lesion at baseline and on treatment if the lesion can be biopsied with acceptable clinical risk (as judged by the investigator).
- Ability to take oral medication
- Patients must have adequate organ and marrow function defined by study-specified laboratory tests
- Must use acceptable form of birth control while on study
- Ability to understand and willingness to sign a written informed consent document
Exclusion Criteria:
- Known history or evidence of brain metastases
- Prior chemotherapy for metastatic disease in castration-resistant prostate cancer
- Had surgery within 4 weeks prior to the first dose of study drug
- Had radiation, biological, or other investigational cancer therapy within 2 weeks prior to the first dose of study drug
- Had second-line hormonal therapy within 2 weeks prior to the first dose of study drug
- Systemic steroids within 1 weeks prior to the first dose of study drug
- Had prior enzalutamide, ARN-509, or galeterone therapy
- Have moderate or severe cardiovascular disease
- Have a history of a seizure
- Have uncontrolled intercurrent illness, including but not limited to ongoing or active infection, systematic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric condition that would limit compliance with study requirements
- Have a history of any autoimmune disease:inflammatory bowel disease, (including ulcerative colitis and Crohn's Disease), rheumatoid arthritis, systemic progressive sclerosis (scleroderma), systemic lupus erythmatosus (SLE) autoimmune vasculitis (e.g., Wegener's Granulomatosis), central nervous system (CNS) or motor neuropathy considered to be of autoimmune origin (e.g., Guillian-Barre Syndrome, Myasthenia Gravis, Multiple Sclerosis)
- Have known history of infection with HIV, hepatitis B, or hepatitis C
学习计划
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:第 1 组:恩杂鲁胺和 LY2157299
|
160mg of enzalutamide is administered orally once a day on days 1-28 of each cycle.
其他名称:
150 mg of LY2157299 is administered orally twice a day on days 1-14 of each cycle.
其他名称:
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实验性的:第 2 组:单独使用恩杂鲁胺
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160mg of enzalutamide is administered orally once a day on days 1-28 of each cycle.
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Progression Free Survival in Patients With Metastatic Castration-resistant Prostate Cancer Treated With Enzalutamide and LY2157299 (Arm 1) Versus Enzalutamide Alone (Arm 2) Using RECIST 1.1 Criteria.
大体时间:8 years
|
8 years
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of Participants With (PSA50) Response
大体时间:4 years
|
PSA50 response in patients with metastatic castration-resistant prostate cancer treated with enzalutamide and LY2157299 |
4 years
|
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Overall Survival (OS) in Patients With Metastatic Castration-resistant Prostate Cancer Treated With Enzalutamide and LY2157299 (Arm 1) Versus Enzalutamide Alone (Arm 2).
大体时间:8 years
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8 years
|
|
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Number of Patients Experiencing Treatment-related Toxicities
大体时间:8 years
|
8 years
|
合作者和调查者
调查人员
- 首席研究员:Channing Paller, MD、Johns Hopkins University
出版物和有用的链接
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- J1557
- IRB00065746 (其他标识符:JHMIRB)
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