US biopharmaceutical company Pfizer Inc (NYSE:PFE) and German biotechnology company BioNTech SE (NASDAQ:BNTX) announced on Thursday that the US Food and Drug Administration (FDA) has approved their 2026-2027 COVID-19 vaccine formula targeting the XFG variant (COMIRNATY XFG).
The vaccine is authorised for adults aged 65 and older and for people aged 5-64 with at least one underlying condition that increases their risk of severe outcomes from COVID-19. This approval is supported by previously submitted clinical, non-clinical and real-world data, along with manufacturing and quality data.
The companies said the XFG-adapted vaccine generated strong immune responses against circulating SARS-CoV-2 variants, including XFG, XFG.1.1, NB.1.8.1, PQ.17 and PQ.2.8.1. The XFG formulation follows FDA guidance for the preferred US COVID-19 vaccine composition beginning in autumn 2026.
Shipments will begin immediately, with the vaccine expected to become available at pharmacies, hospitals and clinics across the United States in the coming days. More than five billion doses of COMIRNATY have been distributed globally to date.
CelLBxHealth secures USD65,000 pharmaceutical research contract
Racura Oncology receives approval for RC220 trial to proceed to higher dose
Blue Lake Biotechnology reports interim data from Phase 1/2a paediatric clinical trial of BLB201
Solvonis signs Portugal agreement to assess European expansion of Phase 3 alcohol addiction trial
ABL Texcell Diagnostics acquires IntegraGen assets to expand into precision oncology
Akeso reports first patient dosed in Phase III study of cadonilimab in colon cancer
Natera secures FDA Breakthrough Device designation for multi-cancer early detection assay
FDA approves Genentech's Tecentriq combination therapy for stage III colon cancer
Alpheus Medical starts new clinical trial of PoMA therapy in butterfly glioblastoma
Sophos IRB and ALCMI partner to support lung cancer research
Northwest Biotherapeutics and NHSBT collaborate to support production of DCVax-L
argenx reports positive Phase 2 results for FB102 in coeliac disease