HLB's US subsidiary scores FDA fast track designation for Merkel cell cancer vaccine

4 November 2022 - HLB said on Friday that the anti-cancer vaccine candidate ITI-3000 aiming to treat Merkel cell cancer ...

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Codagenix receives FDA fast track designation for live attenuated, intranasal RSV vaccine candidate CodaVax-RSV

2 November 2022 - Codagenix today announced that the US FDA has granted fast track designation to CodaVax-RSV, an intranasal, live ...

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GSK’s respiratory syncytial virus older adult vaccine candidate granted priority review by US FDA

2 November 2022 - US FDA has set a Prescription Drug User Fee Act action date of 3 May 2023. ...

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Pfizer COVID vaccine price hike to boost revenue for years, rivals may follow

21 October 2022 - Pfizer's plan to as much as quadruple US prices for its COVID-19 vaccine next year is ...

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US FDA grants emergency use authorisation for Novavax COVID-19 Vaccine, adjuvanted as a booster for adults

19 October 2022 - Novavax today announced that the Novavax COVID-19 Vaccine, Adjuvanted (NVX-CoV2373) has received emergency use authorisation from the ...

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US FDA approves Menveo in a new single vial presentation to help prevent disease caused by meningococcal bacteria serogroups A, C, Y, and W

17 October 2022 - Single vial presentation option removes the need for reconstitution of Menveo before use in individuals 10 ...

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FDA authorises Moderna and Pfizer-BioNTech bivalent COVID-19 vaccines for use as a booster dose in younger age groups

12 October 2022 - Today, the US FDA amended the emergency use authorisations of the Moderna COVID-19 Vaccine, Bivalent and the ...

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FDA approves vaccine for use during third trimester of pregnancy to prevent whooping cough in infants younger than two months of age

7 October 2022 - Today, the US FDA approved Boostrix (Tetanus toxoid, reduced Diphtheria toxoid and acellular Pertussis vaccine, adsorbed) for ...

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Pfizer and BioNTech submit application to U.S. FDA for Emergency Use Authorisation of Omicron BA.4/BA.5 adapted bivalent vaccine booster in children 5 through 11 years of age

26 September 2022 - Pfizer and BioNTech today announced they have completed a submission to the US FDA requesting Emergency Use ...

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Moderna asks FDA to authorise omicron Covid boosters for children as young as 6 years old

23 September 2022 - The Centers for Disease Control and Prevention, in a document published Tuesday, said it expects children to ...

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Statement by President Biden on FDA and CDC authorising updated COVID-⁠19 vaccines

6 September 2022 - This week, we begin a new phase in our COVID-19 response. We are launching a new ...

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FDA grants breakthrough therapy designation to Pfizer’s Group B Streptococcus vaccine candidate to help prevent infection in infants via immunisation of pregnant women

7 September 2022 - Pfizer today announced that its investigational Group B Streptococcus vaccine candidate, GBS6 or PF-06760805, received breakthrough ...

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FDA authorises Moderna, Pfizer-BioNTech bivalent COVID-19 vaccines for use as a booster dose

31 August 2022 - Today, the US FDA amended the emergency use authorisations of the Moderna COVID-19 Vaccine and the Pfizer-BioNTech ...

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FDA expected to authorise Moderna, Pfizer-BioNTech Omicron boosters

29 August 2022 - The move would set the stage for the Biden administration to begin offering the reformulated vaccine shortly ...

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FDA plans to authorise bivalent boosters by Labor Day, sources say

24 August 2022 - The FDA plans to authorise updated versions of Pfizer-BioNTech’s and Moderna’s Covid boosters around Labor Day, ...

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