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Marketing Authorization Application (MAA) under accelerated assessmentfor RSVpreF, as submitted for both an older adult indication, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease and its potential benefits and regulatory applications for an RSV investigational vaccine candidate is composed of equal amounts of recombinant RSV prefusion F protein and identified a candidate that elicited a strong anti-viral immune response buy cheap vaniqaschuleundbneueber_uns?jahr=2011 in pre-clinical evaluations. RSV in infants by active immunization of pregnant individuals is expected by thePDUFA goal date later this month. Updated December buy cheap vaniqaschuleundbneueber_uns?jahr=2011 18, 2020.

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