Pfizer and BioNTech announce submission of initial data to U.S. FDA to support booster dose of COVID-19 vaccine

Pfizer

16 August 2021 - Phase 1 safety and immunogenicity data in individuals who received a third dose of the Pfizer-BioNTech vaccine (BNT162b2) show a favourable safety profile and robust immune responses.

 Pfizer  and BioNTech today announced that they have submitted Phase 1 data to the U.S. FDA to support the evaluation of a third, or booster, dose of the companies’ COVID-19 vaccine (BNT162b2) for future licensure.

Read Pfizer press release

Michael Wonder

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Michael Wonder

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US , Vaccine , Dossier , COVID-19