The U.S. Food and Drug Administration has said it wants at least two
months of safety data before authorizing emergency use of any
experimental coronavirus vaccine.
Based on current trial enrollment and dosing pace, Pfizer expects to
have that safety data in the third week of November, Chief Executive
Officer Albert Bourla said in a statement.
Pfizer had said previously that it expected late-stage trial data in
October. (https://bit.ly/31bWdpP)
(Reporting by Manojna Maddipatla and Manas Mishra in Bengaluru;
Editing by Saumyadeb Chakrabarty)
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