Update (11/30): Moderna will submit its Covid-19 vaccine to the Food and Drug Administration for emergency use authorization after the biotech firm completed its Phase 3 trial, NBC News report. The study found that the vaccine was 94.1% effective at preventing Covid-19, and 100% effective at preventing severe cases (along with the drug needing Fda approval, the study itself still needs to be peer-reviewed). The Fda’s Vaccines and Related Biological Products Advisory Committee will meet and discuss the Moderna vaccine December 17th, one week after it discusses another promising vaccine developed by Pfizer and BioNTech.
- 11/30/2020
- by Jon Blistein
- Rollingstone.com
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