Drug intelligence / Profile preview

monovalent H1N1 influenza virus vaccine

Development stage
Unknown
Lead developer
Novartis
Modality
Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

The monovalent H1N1 influenza virus vaccine, most notably known by the brand name **Focetria**, is an inactivated subunit vaccine developed by **Novartis** to prevent infection from the 2009 pandemic H1N1 influenza A virus. It contains purified surface antigens, specifically hemagglutinin (HA) and neuraminidase (NA), derived from the A/California/7/2009 (H1N1)v-like strain (prepared from the reassortant virus NYMC X-179A). The vaccine is produced in embryonated chicken eggs and is typically formulated with the **MF59** adjuvant, a squalene-based oil-in-water emulsion designed to enhance the magnitude and breadth of the immune response, allowing for dose-sparing. Focetria was granted marketing authorization by the European Medicines Agency (EMA) during the 2009 pandemic and was evaluated in various populations, including children and the elderly, demonstrating high immunogenicity and a manageable safety profile. While Novartis was the original developer, its vaccine business was later acquired by **CSL (Seqirus)** and **GSK**.

Brand names
Focetria
Other names
pandemic influenza vaccine (H1N1) (surface antigen, inactivated, adjuvanted)A/H1N1 MF59-adjuvanted vaccineH1N1v vaccineH-1N1v vaccineH 1N1v vaccineA/H1N1 influenza subunit vaccine
02

Targets

Neuraminidase (Influenza A virus (A/California/07/2009(H1N1)))HA (Hemagglutinin (Influenza A virus A/California/07/2009 (H1N1)))

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