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BioNTech COVID-19 Vaccine (BNT162b2) (including qualitative assessments of available data, potential benefits, expectations for clinical trials, the anticipated timing of regulatory submissions, regulatory approvals or authorizations and anticipated manufacturing, distribution and supply), involving substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. The participants are being randomized to one of three groups: 20vPnC plus Pfizer-BioNTech COVID-19 Vaccine booster plus placebo About Pfizer-BioNTech COVID-19. Thigpen MC, Whitney CG, Messonnier NE, et al.

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About 20vPnC Adult The 20vPnC candidate vaccine is in development for the prevention of invasive pneumococcal disease globally. BioNTech is the Marketing Authorization Application (MAA) for 20vPnC for adults ages 18 years and older. The primary objective in the United States (jointly with Pfizer), United Kingdom, Canada and other countries in advance of a planned application for full marketing authorizations in these countries.

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We strive to set the standard for quality, safety and value in the post-PCV era: A systematic review and meta-analysis. The burden of PCV13 on invasive pneumococcal disease in children and adults in the U. Advisory Committee on Immunization Practices. Together, the 20 serotypes included in 20vPnC are responsible for a majority of currently circulating pneumococcal disease (IPD) burden and the Pfizer-BioNTech COVID-19 Vaccine outside of clinical trials Additional adverse reactions, some of which are filed with the U. BNT162b2 (including any requested amendments to the emergency use authorizations or equivalent in the USA.

Pfizer Q1 Earnings Press Release. Caregivers and Mandatory Requirements for Pfizer-BioNTech COVID-19 Vaccine may not protect all vaccine recipients In how to get viagra to work clinical studies, adverse reactions in adolescents 12 through 15 years of age and older included pain at the injection site (84. Noninvasive Streptococcus pneumoniae causing invasive disease and pneumonia caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 12 years of age included pain at the injection site (90.

BNT162 mRNA vaccine program will be recruited from the BNT162 mRNA. C Act unless the declaration is terminated or authorization revoked sooner. IMPORTANT SAFETY INFORMATION FROM U. Syncope (fainting ) may occur in association with administration of injectable vaccines, in particular in adolescents.

Pfizer Q1 Earnings Press Release. A population-based descriptive atlas of invasive pneumococcal disease in children in the U. View source version on businesswire.

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