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After this important discovery, Pfizer tested numerous versions of a stabilized prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing. NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of medically attended lower respiratory infections due to respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. We routinely post information that may be important to investors on our website at www.
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The bivalent vaccine candidate has the potential to be the first maternal immunization and 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.
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