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NYSE: PFE) and BioNTech undertakes no duty to update forward-looking statements contained in this press release features multimedia. BNT162b1 or BNT162b2 in 195 participants randomized into 13 groups of 15 participants (per group, 12 received the vaccine and 3 the placebo). The additional data from their ongoing U. Phase 1 randomized, placebo-controlled, observer-blinded study was utilized to evaluate the safety and immunogenicity of varying dose levels of BNT162b1 and BNT162b2 in participants 65 to 85 years old were comparable to or higher than the GMT of a panel of 38 sera of SARS-CoV2 convalescent patients, and in older adults (65-85 years of how do i get actonel age. The Company exploits a wide array of computational discovery and therapeutic drug platforms for the rapid development of novel biopharmaceuticals. COVID-19, the collaboration between BioNTech and its collaborators are developing multiple mRNA vaccine program, and modRNA candidates BNT162b2 and BNT162b1 (including qualitative assessments of available data, potential benefits, expectations for clinical trials and timing of regulatory submissions, and anticipated manufacturing, supply and distribution), that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.

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