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Clinical Trial Summary

This is an open label, multi-center, phase 1 safety run-in and phase 2 study of BBI608 in combination with temozolomide in patients with recurrent or progressive glioblastoma who have not received prior bevacizumab therapy.


Clinical Trial Description

In arm A, patients who are candidates for surgical resection will receive BBI608 as monotherapy prior to resection, followed by post-operative BBI608 administered in combination with temozolomide. In arm B, patients who are not candidates for surgical resection will receive BBI608 administered orally, daily, in combination with temozolomide. In the phase 1/dose-limiting toxicity (DLT) cohort portion of this study, pharmacokinetics will be evaluated for both arms A and B. Pharmacodynamics will be evaluated in all patients who undergo surgical resection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02315534
Study type Interventional
Source Sumitomo Pharma America, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 2015
Completion date June 24, 2019

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