COVID-19 vaccine strain updates: global regulators agree on timing and data requirements

17 April 2024 - International regulators have published a report today presenting the outcomes of a workshop on COVID-19 vaccine ...

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GSK’s 5 in 1 meningococcal ABCWY vaccine candidate accepted for regulatory review by US FDA

16 April 2024 - Submission based on results from pivotal Phase III trial showing all primary outcomes met. ...

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EU recommendations for 2024/2025 seasonal flu vaccine composition

26 March 2024 - EMA has issued recommendations for the influenza virus strains that vaccine manufacturers should include in vaccines for ...

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ImmVira's oncolytic product MVR-T3011 IT intratumoral injection receives FDA fast track designation for HNSCC treatment

15 March 2024 - ImmVira has recently announced that the US FDA has granted fast track designation for oncolytic virus product ...

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European Commission approves Pfizer’s Prevenar 20 to help protect infants and children against pneumococcal disease

13 March 2024 - Prevenar 20 (20 valent pneumococcal conjugate vaccine) offers the broadest serotype coverage of any paediatric pneumococcal ...

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COVID-19 2024 vaccine advice

29 February 2024 - The Australian Government has accepted the latest advice from the Australian Technical Advisory Group on Immunisation ...

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New Zealand Pharmaceutical Schedule - 1 March 2024

1 March 2024 - The March 2024 issue of the New Zealand Pharmaceutical Schedule is now available and in effect. ...

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GSK's RSV vaccine, Arexvy, accepted for review by Health Canada for prevention of RSV disease in adults aged 50-59 at increased risk

26 February 2024 - Submission supported by positive results of a Phase 3 study showing immune response and tolerability in adults ...

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COVID-19 vaccine available in March

22 February 2024 - Joint media release with Health New Zealand. ...

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CAN-3110 receives FDA fast track designation for treatment of recurrent high-grade glioma

13 February 2024 - Candel Therapeutics today announced that the US FDA granted fast track designation for CAN-3110 -- a first ...

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MHRA approvals for Comirnaty (Pfizer/BioNTech) and Nuvaxovid (Novavax) COVID-19 vaccines

10 February 2024 - Approval of a change to the licence of Comirnaty COVID-19 vaccine will enable thawing and re-labelling of ...

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GSK’s RSV vaccine, Arexvy, accepted under priority review in US for the prevention of RSV disease in adults aged 50-59 at increased risk

6 February 2024 - Application supported by positive results of a Phase 3 trial showing immune response and acceptable tolerability profile ...

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Ultimovacs receives FDA fast track designation for UV1 cancer vaccine for the treatment of patients with unresectable mesothelioma

5 February 2024 - The designation was granted by the US FDA based on results from the randomised Phase II clinical ...

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GSK’s RSV vaccine, Arexvy, accepted for regulatory review by the EMA for the prevention of RSV disease in adults aged 50-59 at increased risk

29 January 2024 - Application supported by positive results of a Phase 3 trial showing immune response and acceptable tolerability ...

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TGA approves RSV vaccine for use through private prescription for Australians over 60

17 January 2024 - A vaccine for respiratory syncytial virus has been approved by the TGA and will be available through ...

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