This study evaluates the safety and specific antitumor immune responses of mRNA vaccines GV-108 and GV-907 in IDH-wildtype glioblastoma patients.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Eligible patients will receive intradermal injections of cancer vaccines
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China
Adverse Events
Time frame: From baseline, assessed at every study visit through study completion, up to 96 weeks.
Antigen-specific T cell responses in peripheral blood
Time frame: Baseline, Weeks 8-9, 12, 24, 36, 48, 72, and 96
Progression-Free Survival
Time frame: Up to 96 weeks.
Overall Survival
Time frame: Up to 96 weeks.
Objective response rate
Time frame: Up to 96 weeks.
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