FDA approves new vaccine for Influenza A prevention
HOLLY SPRINGS, N.C. -- The U.S. Food and Drug Administration (FDA) has approved AUDENZ™ (Influenza A (H5N1) Monovalent Vaccine, Adjuvanted) to help protect individuals six months of age and older against influenza A (H5N1).1 AUDENZ is the first-ever adjuvanted, cell-based influenza vaccine designed to protect against influenza A (H5N1) in the event of a pandemic. Seqirus, a global leader in influenza prevention and the pandemic response has been granted approval.
Influenza A monovalent vaccine, adjuvanted is an inactivated vaccine indicated for active immunization and is designed with the capability to be rapidly deployed and to be stockpiled for first responders in the event of a pandemic, according to the release from Seqirus. The vaccine was developed through a partnership between Seqirus and the Biomedical Advanced Research and Development Authority (BARDA), which is part of the Office of the Assistant Secretary for Preparedness and Response at the US Department of Health of Human Services.
The novel vaccine combines two leading-edge technologies—MF59® adjuvant and cell-based antigen manufacturing. AUDEN is designed to be rapidly deployed to help protect the U.S. population and can be stockpiled for first responders in the event of a pandemic."The approval of AUDENZ represents a key advance in influenza prevention and pandemic preparedness, combining leading-edge cell-based manufacturing and adjuvant technologies," said Russell Basser, MD, Chief Scientist and Senior Vice President of Research and Development at Seqirus.
"This pandemic influenza vaccine exemplifies our commitment to developing innovative technologies that can help provide a rapid response during a pandemic emergency."An influenza pandemic is a global epidemic caused by the emergence of a new influenza virus to which there is little or no pre-existing immunity in the human population.4 Pandemics are impossible to predict and can cause catastrophic morbidity and mortality globally.
The World Health Organization (WHO) Global Influenza Strategy for 2019-2030 states that a severe pandemic can result in widespread social and economic effects, including a loss of national economic productivity and severe economic burdens on affected citizens and communities.5Influenza vaccines using the MF59® adjuvant may enhance and broaden the body's immune response by inducing antibodies against virus strains that have mutated.
This adjuvant is an important part of pandemic preparedness planning as it reduces the amount of antigen required to produce an immune response, increasing the number of doses of the vaccine developed so that a large number of people can be protected as quickly as possible. The cell-based vaccine antigen, MF59® adjuvant, and formulated prefilled syringes used in the AUDENZ vaccine are all produced in the state-of-the-art Seqirus production facility in Holly Springs, N.C., built and supported through a multi-year public-private partnership between Seqirus and the Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response at the U.S. Department of Health and Human Services.11"Pandemic influenza viruses can be deadly and spread rapidly, making a production of safe, effective vaccines essential in saving lives," said BARDA Director Rick Bright, PhD.
"With this licensure – the latest FDA-approved vaccine to prevent H5N1 influenza – we celebrate a decade-long partnership to achieve health security goals set by the National Strategy for Pandemic Influenza and the 2019 Executive Order to speed the availability of influenza vaccine. Ultimately, this latest licensure means we can protect more people in an influenza pandemic."Seqirus is uniquely positioned to manufacture cell-based vaccines on a pandemic scale as a result of its public-private partnership with the BARDA