Novavax Announces Positive Data From Phase 2 Trial of Quadrivalent Seasonal Influenza VLP
Novavax’ technology platform enables the creation of recombinant, strain-specific VLPs. Novavax’ Seasonal Influenza VLP consists of VLPs representing four different strains of influenza virus, each expressing strain-specific hemagglutinin and neuraminidase antigens. This dose-ranging clinical trial was designed to evaluate the safety and immunogenicity of the Seasonal Influenza VLP in 400 healthy adults. The primary outcomes of the trial assessed safety and tolerability of the Seasonal Influenza VLP and quantified immune responses to each of the four influenza strains based on hemagglutination-inhibiting antibody titers. The secondary outcomes evaluated neuraminidase-inhibiting antibody titers for all four influenza strains.
“Titers of antibodies that inhibit hemagglutination by the influenza virus – called hemagglutination-inhibiting or HAI antibodies – remain the best-accepted correlates of the protection provided by influenza vaccines. We were very pleased to see that our Seasonal Influenza vaccine candidate elicited increases in HAI titers for all four viral strains that would allow our vaccine to fulfill CBER’s criteria for accelerated approval,” said
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Contact:Novavax, Inc. Barclay A. Phillips SVP, Chief Financial Officer and TreasurerAndrea N. Flynn , Ph.D. Senior Manager, Investor Relations [email protected] 240-268-2000Russo Partners, LLC David Schull Todd Davenport , Ph.D. [email protected][email protected] 212-845-4271
