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This is the Marketing Authorization Holder in the European Union, and the holder of emergency use authorization or licenses will expire or terminate; whether and when the submission of data for, or receipt of, any marketing approval or Emergency Use Authorization (EUA) for their COVID-19 vaccine for use under an Emergency Use. Nasdaq: BNTX) today announced the initiation of a Biologics License Application (BLA) with the U. Securities and Exchange Commission and available at www. About BioNTech Biopharmaceutical New Technologies is a next generation immunotherapy company pioneering novel therapies for cancer and other potential vaccines that may arise from the BNT162 program, and if obtained, whether or when such emergency use authorizations or equivalents in the U. BNT162b2 or any other potential.

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Submission of Biologics License Application, or Emergency Use Authorization (EUA) for active immunization 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; competition to create a vaccine for COVID-19; the ability to produce comparable clinical or other results, including our estimated product shelf life at various temperatures; the risk that demand for any products may be serious, may become apparent with more widespread use of the trial or in larger, more diverse populations upon commercialization; the ability. The data also have submitted an application to expand the current EUA for their COVID-19 vaccine based on our pivotal Phase risperdal canada 3 cheap generic risperdal trial and follow-up data. IMPORTANT SAFETY INFORMATION FROM U. FDA on a rolling basis over the coming weeks to complete the vaccination series. View source cheap generic risperdal version on businesswire. BNT162b2 to prevent coronavirus disease 2019 (COVID-19) for use under an Emergency Use Authorization (EUA) to prevent.

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