However, the DNA needs to be conserved at -80°C, which complicates worldwide distribution enormously.
The vaccine, still at the clinical trials phase and involving 44 000 volunteers and 154 testing sites across the US, may qualify for “Emergency Use Authorization”, granted by drug safety authorities in the country. This EUA can only be put in place 2 months after half of the trial’s participants have received their last dose of the vaccine.
For the moment the United States has ordered 100 million doses of the vaccine and the EU 300 million. However, even if in a best-case scenario the vaccine began to be commercialised before the end of the year, restrictive sanitary measures would continue during the vaccination period. It’s clear that social distancing will not be ending in the immediate future.