A Three-part, Phase I/II Dose-Escalation Study to Define the Safety, Tolerability, and Optimal Dose of Candidate GBM vaccine VBI-1901 with Subsequent Extension of Optimal Dose in Recurrent GBM subjects (Brain Tumors)
Study of Vaccine for Cytomegalovirus (CMV) in Patients with Brain Tumors
Sponsor: VBI Vaccines, Inc.
Enrolling: Male and Female Patients
IRB Number: AAAR5300
U.S. Govt. ID: NCT03382977
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this study is to test the safety of a new vaccine, VBI-1901, and to know more about its ability to boost the response of the immune system against Cytomegalovirus. The reason for testing this vaccine in people with a brain tumor is that it might one day be used to boost the ability of the immune system to fight a certain type of brain tumor. This type of treatment for brain tumors is called immunotherapy.
Investigator
Andrew Lassman, MD
Do You Qualify?
Are you between the ages of 18-70? Yes No
Have you been diagnosed with a glioblastoma (type of brain cancer)? Yes No
Has your tumor come back or progressed after an initial treatment? Yes No
Have you recovered from surgery? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162
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