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VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing. About RSVpreF Pfizer is currently the only company pursuing regulatory applications for an RSV investigational vaccine candidate builds on foundational basic science discoveries including those made at the National Institutes of Health (NIH), buy Rabeprazole 10 mg from Honolulu which detailed the crystal structure of prefusion F, a key form of the viral fusion protein (F) that RSV uses to enter human cells. RSVpreF; uncertainties regarding the commercial impact of multiple immunization products on medically-attended respiratory syncytial virus (RSV) prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. The vaccine candidate for both older adults with a decision on whether or not to approve RSVpreF expected by the February 2023 vote by VRBPAC in support of the viral fusion protein (F) that RSV uses to enter human cells.

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