The Advisory Committee on Immunization Practices' Interim Recommendation for Use of Moderna COVID-19 Vaccine - United States, December 2020.

@article{Oliver2021TheAC,
  title={The Advisory Committee on Immunization Practices' Interim Recommendation for Use of Moderna COVID-19 Vaccine - United States, December 2020.},
  author={Sara E Oliver and J. Gargano and M. Marin and Megan Wallace and K. Curran and M. Chamberland and Nancy McClung and D. Campos-Outcalt and R. Morgan and Sarah A. Mbaeyi and J. Romero and H. Talbot and G. Lee and B. Bell and Kathleen Dooling},
  journal={MMWR. Morbidity and mortality weekly report},
  year={2021},
  volume={69 5152},
  pages={
          1653-1656
        }
}
On December 18, 2020, the Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the Moderna COVID-19 (mRNA-1273) vaccine (ModernaTX, Inc; Cambridge, Massachusetts), a lipid nanoparticle-encapsulated, nucleoside-modified mRNA vaccine encoding the stabilized prefusion spike glycoprotein of SARS-CoV-2, the virus that causes coronavirus disease 2019 (COVID-19) (1). This vaccine is the second COVID-19 vaccine authorized under an EUA for the prevention of COVID-19 in the… Expand
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