Pfizer Inc. pulled into a virtual tie with GSK plc in the five-company race to bring to market a new vaccine to prevent respiratory syncytial virus (RSV) infections, announcing data on 25 August that show its bivalent candidate RSVpreF demonstrated efficacy in adults 60 and older with two or more symptoms of related lower respiratory tract infections and in patients with three or more symptoms as well.
GSK said on 10 June that its adjuvanted protein vaccine candidate, GSK3844766A, showed what it called “exceptional” results in healthy volunteers aged 60 and older, but unlike Pfizer, did not release numerical data from its Phase III study. (Also see "GSK Registers A Win For Older People RSV Vaccine – But Awaited Data Will Be Crucial" - Scrip, 10 June, 2022.) Pfizer’s top-line data readout from its Phase III RENOIR trial showed vaccine efficacy in 66
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