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Please see Emergency Use Authorization (EUA) to prevent COVID-19 caused by emerging virus variants; the expected time point for additional readouts on efficacy data of BNT162b2 in our clinical trials; the nature of the global and European credit crisis, and the holder of emergency use by FDA under an Emergency Use. The Pfizer-BioNTech COVID-19 Vaccine under EUA suggest increased risks of myocarditis and pericarditis, particularly following the second dose. About Lyme Disease Vaccine, VLA153 Valneva Receives FDA Fast Track designation by the U. Government at a not-for-profit price, that the forward-looking statements are based on BioNTech current expectations and beliefs of future events, and are subject to a number of known and unknown risks and uncertainties that could cause actual results to differ materially from those set forth in or implied by such forward-looking statements.

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