BENITIONSClinical Trial Intelligence

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
分期1期
申办方National Cancer Institute (NCI)
状态进行中(已停止招募)
受试者人数50 人
干预(药物)Bevacizumab, Laboratory Biomarker Analysis, Pharmacological Study, Sapanisertib
开始日期2014年5月20日
完成日期2020年12月31日
结果公布日2023年10月4日

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/RP2D5 mg/day

Most Common Related Toxicities That Led to Dose Hold/Reductions

Up to 2 years · participants

Dose Level 1 - 3 mg MLN0128 Daily0 participants
Dose Level 2 - 4 mg MLN0128 Daily0 participants
Dose Level 3 - 5 mg MLN0128 Daily2 participants
Dose Level 1 - 3 mg MLN0128 Daily0 participants
Dose Level 2 - 4 mg MLN0128 Daily0 participants
Dose Level 3 - 5 mg MLN0128 Daily1 participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

同一适应症的其他试验

全部试验

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。