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The VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate RSVpreF or PF-06928316. These results buy myambutol 1000 mg online from wisconsinschuleundbne were also recently published in The New England Journal of Medicine. The vaccine candidate is currently the only company pursuing regulatory applications for an RSV investigational vaccine candidate. The bivalent vaccine candidate 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. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing.

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