PHARMAC expands access to meningococcal B vaccine for children under 5

31 July 2025 - PHARMAC is extending access to the meningococcal B vaccine (Bexsero), with up to 77,000 more children ...

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EMA CHMP adopts positive opinion recommending authorisation of Moderna's COVID-19 mRNA vaccine targeting the SARS-CoV-2 variant LP.8.1

25 July 2025 - Moderna's updated COVID-19 mRNA vaccine will be available for the 2025-2026 vaccination season, pending a European ...

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Pfizer and BioNTech receive positive CHMP opinion for LP.8.1 adapted COVID-19 vaccine in the European Union

25 July 2025 - Data indicate that the LP.8.1-adapted COVID-19 vaccine confers improved immune response against currently dominant and emerging sub-lineages ...

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Bavarian Nordic receives acceptance from Health Canada for review of the new drug submission for its chikungunya vaccine

22 July 2025 -  Bavarian Nordic announced today that Health Canada has accepted for review the Company’s application for licensure ...

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US FDA approves GSK’s Shingrix in a pre-filled syringe presentation

17 July 2025 - Pre-filled syringe presentation offers a convenient administration option to health care professionals. ...

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Call for RSV vaccine subsidies for elderly as severe hospitalisations on rise

16 July 2025 - RSV has outstripped severe Covid and flu hospitalisation rates and proved itself more fatal than either of ...

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US FDA accepts application to review expanded use of GSK’s RSV vaccine, Arexvy, for adults 18-49 at increased risk

14 July 2025 - FDA decision anticipated H1, 2026 ...

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Moderna receives full US FDA approval for COVID-19 vaccine, Spikevax, in children aged 6 months through 11 years at increased risk for COVID-19 disease

10 July 2025 - Spikevax is now approved for all adults aged 65 years and older, and individuals aged 6 ...

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GSK’s RSV vaccine, Arexvy, accepted for regulatory review by the EMA to expand use in adults 18 years and older

13 June 2025 - Regulatory decision anticipated H1, 2026. ...

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Moderna receives US FDA approval for RSV vaccine, mRESVIA, in adults aged 18–59 at increased risk for RSV disease

12 June 2025 - Expanded indication builds on existing US FDA approval of mRESVIA for adults aged 60 and older. ...

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Oxford vaccine against deadly Nipah virus granted EMA PRIME designation

11 June 2025 - The University of Oxford’s vaccine to protect people from deadly Nipah virus has been granted support from ...

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Moderna receives US FDA approval for COVID-19 vaccine mNEXSPIKE

31 May 2025 - mNEXSPIKE becomes Moderna's third FDA approved product. ...

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Pfizer and BioNTech submit EMA application for COVID-19 vaccine targeting LP.8.1 for 2025-2026 season

28 May 2025 -  2025 -- Pfizer and BioNTech today announced that they have submitted a regulatory application to the ...

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Moderna files FDA application for the LP.8.1 targeting COVID-19 vaccine

23 May 2025 - Moderna today announced that it has submitted an application to the US FDA for review of its ...

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Moderna provides update on BLA submission for combination vaccine against influenza and COVID-19

21 May 2025 -  Moderna today announced that in consultation with the US FDA, the Company has voluntarily withdrawn the ...

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