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.
Labcorp to offer FDA-cleared pTau-217 blood test for Alzheimer's assessment
Tempus announces receipt of FDA clearance for AI pulmonary hypertension detection product
European Commission grants orphan designation for Vanda's imsidolimab
United Therapeutics wins FDA acceptance for ralinepag PAH filing
Acadia wins EU approval for DAYBU as first treatment for Rett syndrome
Gilead expands Trodelvy role in first-line metastatic triple-negative breast cancer in Europe
GSK's Jemperli wins FDA priority review for advanced rectal cancer
European Commission grants orphan designation for Lundbeck's asedebart
Pulnovo Medical commences enrolment in PULSE-LHD IDE clinical trial
Nuvation Bio's safusidenib granted FDA Fast Track Designation for IDH1-mutant glioma treatment