The approvals and authorizations come amid a late summer surge in the virus that is tracking a bit earlier than the early fall wave in the US in 2023.
FDA has approved and granted an Emergency Use Authorization (EUA) for the updated, 2024–2025 formulas of messenger RNA (mRNA) vaccines manufactured by Moderna and Pfizer, as announced in a press release on Aug. 22, 2024 (1). These vaccines include a monovalent, or single, component corresponding to the Omicron variant KP.2 strain of SARS-CoV-2.
In a separate press release, Pfizer said its version would begin shipping “immediately” and would be available in pharmacies, hospitals, and clinics across the United States within days (2).
“Vaccination continues to be the cornerstone of COVID-19 prevention,” said Peter Marks, MD, PhD, director of FDA’s Center for Biologics Evaluation and Research, in the FDA press release. “These updated vaccines meet the agency’s rigorous, scientific standards for safety, effectiveness, and manufacturing quality. Given waning immunity of the population from previous exposure to the virus and from prior vaccination, we strongly encourage those who are eligible to consider receiving an updated COVID-19 vaccine to provide better protection against currently circulating variants.”
In anticipation that SARS-CoV-2 variants would continue to develop and emerge, in April 2024 the European Medicines Agency (EMA) published a report, stemming from a workshop in February 2024, on COVID-19 vaccine strains (3). At that time, EMA stressed the importance of developing updated vaccines and reviewing them for approval.
Without even predicting 2024’s late-summer COVID surge, the February workshop anticipated the timeline by which updated vaccines would most likely need to be approved and made available.
“Looking at the global picture, a strain recommendation by regulatory authorities in November/December or April/May should allow all authorized vaccine technologies (mRNA, protein/adjuvanted, inactivated) to meet the start of the autumn vaccination campaign in both hemispheres,” the report, Global Perspectives on COVID-19 Vaccines Strain Update, said (3).
“International convergence on the process and timing of COVID-19 vaccine strain updates are therefore critical in view of the continuous evolution of SARS-CoV-2,” EMA said in a press release detailing the April report (4).
FDA notified manufacturers in June 2024 that the 2024–2025 formula should be a monovalent JN.1-lineage vaccine, and later updated that guidance to inform those manufacturers that KP.2 should be the targeted strain, if possible (1).
FDA published the following guidelines for those wishing to be vaccinated:
1. FDA. FDA Approves and Authorizes Updated mRNA COVID-19 Vaccines to Better Protect Against Currently Circulating Variants. Press Release. Aug. 22, 2024.
2. Pfizer. Pfizer and BioNTech Receive US FDA Approval & Authorization for Omicron KP.2-adapted COVID-19 Vaccine. Press Release. Aug. 22, 2024.
3. Haigney, S. Report on COVID-19 Vaccine Strains Promotes Updates on Vaccine Compositions. BioPharmInternational.com, Apr. 22, 2024.
4. EMA. COVID-19 Vaccine Strain Updates: Global Regulators Agree on Timing and Data Requirements. Press Release. Apr. 17, 2024.
Texas' MD Anderson Cancer Center Creates New Cell Therapy Institute
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