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Seqirus' Audenz Receives the US FDA's Approval as the First Adjuvanted Cell-Based Pandemic Influenza A (H5N1) Vaccine

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Seqirus' Audenz Receives the US FDA's Approval as the First Adjuvanted Cell-Based Pandemic Influenza A (H5N1) Vaccine

Shots:

  • The US FDA has approved Audenz (Influenza A (H5N1) monovalent vaccine- adjuvanted) to protect patients aged ≥6mos. against influenza A
  • The novel vaccine combines two technologies i.e- MF59 adjuvant and cell-based antigen manufacturing. The MF59 adjuvant and formulated prefilled syringes used in the Audenz vaccine- produced in the facility at Holly Springs- NC- supported by its partnership with the BARDA
  • Audenz is the first and only adjuvanted- cell-based pandemic vaccine- designed to provide active immunization against the influenza A virus H5N1 strain and has received FDA’s FT designation to prevent pandemic influenza caused by A (H5N1) virus in Dec’2015

Click here ­to­ read full press release/ article | Ref: PRNewswire | Image: WRAL Techwire


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This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

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