Drug intelligence / Profile preview

trivalent influenza split vaccine

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

Overview

**Trivalent influenza split vaccine** is an inactivated, split-virion vaccine that provides active immunization against influenza by inducing antibodies to the hemagglutinin antigens of three influenza virus strains. Each annual formulation contains two influenza A subtypes (typically H1N1 and H3N2) and one influenza B lineage virus (currently B/Victoria)[1][3][5][7]. The "split" process involves disruption of viral particles, usually with detergents like sodium deoxycholate, to reduce reactogenicity while retaining immunogenic components (mainly hemagglutinin and neuraminidase)[5][7]. The 2024–2025 US formulation includes: - A/Victoria/4897/2022 (H1N1)pdm09-like virus - A/Thailand/8/2022 (H3N2)-like virus - B/Austria/1359417/2021 (B/Victoria lineage)-like virus Vaccines are typically administered intramuscularly, and use may include single or multi-dose vials, some with preservative (thimerosal) in multi-dose format[5][7]. The vaccine is indicated for annual prevention of influenza in adults and children 6 months and older[7]. The mechanism of action is immunization against circulating strains by generating adaptive (humoral) immune responses to viral proteins (mainly hemagglutinin).

Brand names
FLULAVALAfluriaFluzone
Other names
trivalent influenza vaccinetrivalent seasonal influenza vaccineTIVtrivalent inactivated influenza vaccinetrivalent split-virion vaccineinfluenza virus vaccine (trivalent, split)
02

Targets

HA (Hemagglutinin)

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