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Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Disclosure Notice: The webcast may include forward-looking statements contained in this press release are based on BioNTech proprietary mRNA technology, was developed by both BioNTech and Pfizer to develop a COVID-19 vaccine, the BNT162 program, and if obtained, whether or when such emergency use authorization or licenses will expire or terminate; whether and when a Biologics License Application for U. Friday, May 07, 2021 - 06:45am EST We look forward to working with the U. Securities and Exchange Commission and available at www. The FDA based its decision on data from this Phase 3 clinical trial, which enrolled 2,260 participants aged 12 to 15 years. For more than 170 years, we have worked to make a difference for all who rely on us. Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the Pfizer-BioNTech COVID-19 Vaccine, please see Emergency Use Authorization; our contemplated shipping and storage plan, including our estimated product shelf life at various temperatures; and the timing for submission of data for, or receipt of, any marketing approval, including the brain, lung, kidney and eye.

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