Drug intelligence / Profile preview

prepandemic influenza vaccine (h5n1) (surface antigen, inactivated, adjuvanted)

Development stage
Approved
Lead developer
CSL Seqirus
Modality
Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

Aflunov is a prepandemic monovalent, subunit, inactivated influenza vaccine designed to provide active immunization against the H5N1 subtype of Influenza A virus (avian influenza). Originally developed by Novartis Vaccines and Diagnostics and now managed by CSL Seqirus, the vaccine contains 7.5 μg of hemagglutinin (HA) surface antigen derived from the A/Vietnam/1194/2004 (H5N1) strain. It is adjuvanted with MF59, an oil-in-water emulsion, to enhance the immune response by promoting the recruitment and activation of antigen-presenting cells. The vaccine is indicated for use in individuals aged 6 months and older to prepare for or respond to an H5N1 pandemic. It received European Union marketing authorization in 2011.

Brand names
Aflunov
Other names
Novartis Investigational H5N1 vaccineadjuvanted H5N1 vaccineH5N1 influenza vaccineH-5N1 influenza vaccineH 5N1 influenza vaccineInfluenza A virus A/Vietnam/1194/2004 (H5N1) antigen (formaldehyde inactivated)
02

Targets

Sialoglycan (Cell-surface sialoglycan)BCR (Immunoglobulin G B Cell Receptor)H5 HA (Influenza A hemagglutinin H5)

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