BioNTech and Pfizer announced today that the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) has granted a temporary authorization for emergency use for their COVID-19 vaccine BNT162b2.
This constitutes the first Emergency Use Authorization for the vaccine anywhere in the world.
The MHRA’s decision is based on a rolling submission, including data from the Phase III clinical study, which demonstrated a vaccine efficacy rate of 95%.
Pfizer and BioNTech have an agreement with the UK to supply 40 million doses of the BNT162b2; the delivery will occur throughout 2020 and 2021 in stages to ensure an equitable allocation of vaccines across the geographies with executed contracts.
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