COVID-19 vaccines: In the rush for regulatory approval, do we need more data?

BMJ

18 May 2021 - After rollout under emergency authorisation, manufacturers of COVID-19 vaccines now have their sights on regulatory approval. 

But what’s the rush, asks Peter Doshi, and is just six months of data from now unblinded trials acceptable?

In April 2021, Pfizer and Moderna announced efficacy results at the six month mark from the phase III trials of their respective COVID-19 vaccines.

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Michael Wonder

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Michael Wonder

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US , Regulation , Vaccine , Data , COVID-19