Drug intelligence / Profile preview

bioCSL Trivalent Influenza Virus Vaccine

Development stage
Unknown
Lead developer
CSL Seqirus
Modality
Whole Inactivated Vaccines → Inactivated Vaccines → Prophylactic Vaccines → Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

The bioCSL Trivalent Influenza Virus Vaccine is an inactivated, split-virion seasonal influenza vaccine formulated to provide active immunization against three strains of influenza virus. The trivalent formulation contains two influenza A subtypes (H1N1 and H3N2) and one influenza B virus (B/Victoria lineage). The specific viral strains included are selected annually based on global surveillance data and recommendations from health authorities such as the FDA and WHO. For the 2024–2025 season, the recommended composition includes an A(H1N1)pdm09-like virus, an A(H3N2)-like virus, and a B/Victoria-lineage-like virus[1][2][5]. The vaccine works by inducing neutralizing antibodies against hemagglutinin surface proteins of the included viruses, thereby preventing infection or reducing disease severity upon exposure to circulating strains. It is indicated for annual vaccination to prevent seasonal flu in individuals aged 6 months and older[2][5]. Developed originally by bioCSL (now part of CSL Seqirus), this product is manufactured using egg-based technology.

Brand names
bioCSL Trivalent Influenza Virus Vaccine
Other names
CSL Seqirus trivalent influenza vaccineAfluria Trivalent (historical)bioCSL TIV
02

Targets

HA (Hemagglutinin)

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