Drug intelligence / Profile preview

inactivated influenza vaccine (split virion)

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

Overview

Inactivated influenza vaccine (split virion) is a vaccine comprised of highly purified surface and internal antigens from inactivated influenza viruses grown in embryonated chicken eggs. The viral particles are chemically disrupted ("split") to reduce reactogenicity while retaining immunogenic components (mainly haemagglutinin and neuraminidase). The vaccine formulation typically contains antigens from two influenza A subtypes (H1N1, H3N2) and one or two influenza B lineages, conforming to annual WHO recommendations. Upon intramuscular administration, it activates the immune system to produce specific antibodies against the included strains’ haemagglutinins, thereby conferring protective immunity against seasonal influenza infection. The protective effect generally lasts for 6–12 months. It is primarily indicated for annual prophylactic immunization against influenza in children (from 6 months or 6 years, depending on local indications) and adults, including older adults. None of the vaccine's components can cause influenza disease[1][2][3][4][5].

Brand names
FLU-MFLUVIRALIDflu
Other names
inactivated influenza vaccine (split virion)split virion influenza vaccinesplit virus influenza vaccinequadrivalent influenza vaccine (split virion, inactivated)trivalent influenza vaccine (split virion, inactivated)
02

Targets

HA (Hemagglutinin)Neuraminidase

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