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Study identifier: NCT03382977 Synced from ClinicalTrials.gov · July 31, 2026
● Terminated

Study to Evaluate Safety, Tolerability, and Optimal Dose of Candidate GBM Vaccine VBI-1901 in Recurrent GBM Subjects

Condition: Glioblastoma Multiforme  ·  Sponsor: VBI Vaccines Inc.

PhasePhase 1/Phase 2
Planned participants70
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to assess the safety and tolerability of VBI-1901 in subjects with recurrent malignant gliomas (glioblastoma, or GBM).

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (12)

University of California, IrvineIrvine, California, United States
University of California, San DiegoLa Jolla, California, United States
University of California, Los Angeles Neuro-Oncology ProgramLos Angeles, California, United States
StanfordStanford, California, United States
Miami Cancer InstituteMiami, Florida, United States
Massachusetts General HospitalBoston, Massachusetts, United States
Dana-Farber Cancer InstituteBoston, Massachusetts, United States
The Valley Hospital - Neurosurgeons of New JerseyRidgewood, New Jersey, United States
The Neurological Institute of New York Columbia University Medical CenterNew York, New York, United States
Vanderbilt University Medical CenterNashville, Tennessee, United States
MD Anderson Cancer CenterHouston, Texas, United States
Providence - Swedish Medical CenterSeattle, Washington, United States

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Source record: clinicaltrials.gov/study/NCT03382977