CI

At a glance

ClinicalIndex Comparison Record
Phase 1Active· 50 enrolled / 50 target
Drug / intervention
Bevacizumab +3 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02142803
NCT02142803Phase 1ActiveUpdate Overdue (0.3/mo)Completion was 65mo ago

A Phase 1 Study of MLN0128 and Bevacizumab in Patients With Recurrent Glioblastoma and Other Solid Tumors

National Cancer Institute (NCI)·interventional·Posted May 20, 2014·Updated Jun 26, 2026

In Brief

A Phase 1 clinical trial evaluating Bevacizumab, Laboratory Biomarker Analysis, and 2 other interventions for Adult Glioblastoma and 23 related conditions. Active but no longer recruiting, targeting 50 participants across 3 sites.

Signals

Enrollment appears stalled

Detailed Summary

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.

Study Details

Timeline

Phase 1Active
2015201620172018201920202021202220232024202520262027
First PostedMay 20, 2014
Enrollment StartMay 20, 2014
Primary CompletionDec 31, 2020
Study CompletionOct 16, 2026
TodayJul 2, 2026
Enrollment to primary: 6.6 yearsPosted 12.1 years ago

Arms & Interventions

Treatment (TORC1/2 inhibitor INK128, bevacizumab)experimental

Patients receive TORC1/2 inhibitor INK128 PO QD on days 1-28 and bevacizumab IV on days 1 and 15. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Biological: BevacizumabOther: Laboratory Biomarker AnalysisOther: Pharmacological StudyDrug: Sapanisertib

Interventions

Bevacizumabbiological

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Pharmacological Studyother

Correlative studies

Sapanisertibdrug

Given PO