VBI Vaccines Inc VBIV has presented updated 12-month and 18-month overall survival (OS) data from the Phase 2a study of VBI-1901, the Company's recurrent glioblastoma (GBM) vaccine
- VBI-1901 + granulocyte-macrophage colony-stimulating factor (GM-CSF) arm showed 18-month OS of 30% (n=3/10)
- One patient is still on protocol past week 86, with a 93% tumor reduction relative to initiation of treatment at the beginning of the study.
- Two additional patients achieved OS of at least 20 months but are no longer on the protocol.
- VBI-1901 + GlaxoSmithKline Plc's GSK AS01 adjuvant system arm showed 12-month OS of 70% (n=7/10) and 18-month OS not yet reached.
- Historical control data have demonstrated OS to be around 60% at 6-months and about 30% at 12-months after treatment with a monotherapy.
- VBI expects to assess VBI-1901 in randomized, controlled clinical studies in both primary and recurrent GBM patients.
- The Company plans to start enrollment of patients with recurrent GBM in Q1 2022.
- Beginning mid-year 2022, VBI expects to evaluate VBI-1901 in INSIGhT Phase 2 adaptive platform trial with primary GBM.
- Also see: FDA Approves VBI Vaccines' 3-Antigen Hepatitis B Vaccine.
- Price Action: VBIV shares are down 7.69% at $2.88 during the premarket session on the last check Thursday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
Posted In: BiotechNewsPenny StocksHealth CareSmall CapMoversTrading IdeasGeneralbrain cancerBrain TumorBriefsPhase 2 Trial
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in