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10.1038/s41591-021-01230-y

http://scihub22266oqcxt.onion/10.1038/s41591-021-01230-y
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33469205!ä!33469205

suck abstract from ncbi

pmid33469205      Nat+Med 2021 ; 27 (2): 205-211
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  • Looking beyond COVID-19 vaccine phase 3 trials #MMPMID33469205
  • Kim JH; Marks F; Clemens JD
  • Nat Med 2021[Feb]; 27 (2): 205-211 PMID33469205show ga
  • After the recent announcement of COVID-19 vaccine efficacy in clinical trials by several manufacturers for protection against severe disease, a comprehensive post-efficacy strategy for the next steps to ensure vaccination of the global population is now required. These considerations should include how to manufacture billions of doses of high-quality vaccines, support for vaccine purchase, coordination of supply, the equitable distribution of vaccines and the logistics of global vaccine delivery, all of which are a prelude to a massive vaccination campaign targeting people of all ages. Furthermore, additional scientific questions about the vaccines remain that should be answered to improve vaccine efficacy, including questions regarding the optimization of vaccination regimens, booster doses, the correlates of protection, vaccine effectiveness, safety and enhanced surveillance. The timely and coordinated execution of these post-efficacy tasks will bring the pandemic to an effective, and efficient, close.
  • |*Clinical Trials, Phase III as Topic[MESH]
  • |COVID-19 Vaccines/*immunology[MESH]
  • |COVID-19/epidemiology/*immunology/virology[MESH]
  • |Humans[MESH]
  • |Immunity, Herd[MESH]
  • |SARS-CoV-2/*physiology[MESH]


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