The purpose of this study is to evaluate the safety, tolerability and efficacy of VB-111 in patients with Relapsed Glioblastoma Multiforme.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
75
Upon progression, subjects will receive a combination therapy of VB-111 and standard of care bevacizumab
Dana Farber Cancer Institute
Boston, Massachusetts, United States
Duke University Medical Center
Durham, North Carolina, United States
Uthsc- Ctrc
San Antonio, Texas, United States
Tel Aviv Sourasky Medical Center
Tel Aviv, Israel
Overall Survival
Time frame: From date of study entry until the date of death from any cause (up to 10 years)
Progression Free Survival
Time frame: 6 months
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