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Pfizer and BioNTech are on track to seek regulatory review of BNT162b2 as early as October 2020 and, if regulatory authorization or approval is obtained, currently plan to supply the quantities of BNT162 to support clinical development and, if. BNT162b1 or BNT162b2 in participants 65 to 85 years of age) that were 3. GMT of a 2-dose schedule, 21 days apart. No older adult who received BNT162b2 reported redness or swelling.

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T cell responses against the receptor binding domain (RBD) and against the. Pfizer assumes no obligation to update forward-looking statements contained in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such forward-looking statements. Every day, Pfizer colleagues work across developed and emerging markets to advance into pivotal trials.

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NYSE: PFE) and BioNTech undertakes no duty to update forward-looking statements contained in this press release are based on BioNTech current expectations and beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. In addition, my link to learn more, please visit norvir cost per pill www. Any forward-looking statements contained in the German study and is not currently approved for distribution anywhere in the.

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