TORC1/2 Inhibitor MLN0128 and Bevacizumab in Treating Patients With Recurrent Glioblastoma or Advanced Solid Tumors
1期
进行中(已停止招募)
NCT02142803
| 适应症 | Adult Glioblastoma, Endometrial Clear Cell Adenocarcinoma, Endometrial Serous Adenocarcinoma, Ovarian Clear Cell Cystadenocarcinoma |
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| 分期 | 1期 |
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| 申办方 | National Cancer Institute (NCI) |
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| 状态 | 进行中(已停止招募) |
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| 受试者人数 | 50 人 |
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| 干预(药物) | Bevacizumab, Laboratory Biomarker Analysis, Pharmacological Study, Sapanisertib |
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| 开始日期 | 2014年5月20日 |
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| 完成日期 | 2020年12月31日 |
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| 结果公布日 | 2023年10月4日 |
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摘要
This phase I trial studies the side effects and best dose of raptor/rictor-mammalian target of rapamycin (mTOR) (TORC1/2) inhibitor MLN0128 when given in combination with bevacizumab in treating patients with glioblastoma, a type of brain tumor, or a solid tumor that has spread and not responded to standard treatment. TORC1/2 inhibitor MLN0128 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as bevacizumab, may interfere with the ability of tumor cells to grow and spread. Bevacizumab may also stop the progression of tumors by blocking the growth of new blood vessels necessary for tumor growth.
Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (R2PD) of Daily Oral MLN0128 When Administered With Bevacizumab
28 days · mg/day
| Stage 1: Dose Escalation to Estimate MTD/RP2D | 5 mg/day |
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Most Common Related Toxicities That Led to Dose Hold/Reductions
Up to 2 years · participants
| Dose Level 1 - 3 mg MLN0128 Daily | 0 participants |
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| Dose Level 2 - 4 mg MLN0128 Daily | 0 participants |
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| Dose Level 3 - 5 mg MLN0128 Daily | 2 participants |
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| Dose Level 1 - 3 mg MLN0128 Daily | 0 participants |
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| Dose Level 2 - 4 mg MLN0128 Daily | 0 participants |
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| Dose Level 3 - 5 mg MLN0128 Daily | 1 participants |
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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。