New York: As America begins a historic vaccination campaign, the US Food and Drug Administration posted a preliminary analysis confirming the safety and effectiveness of the Covid-19 vaccine developed by Moderna in collaboration with the National Institutes of Health, bringing it ever closer to an emergency use authorisation.
Moderna's vaccine is based on the same technology as Pfizer's - mRNA. The actual virus is not embedded inside these vaccines and people who get the shots can't catch the virus from it. Instead, the vaccine contains a piece of genetic code that trains the body's immune system to recognize the spike protein on the surface of the Covid-19 virus and helps mount an organic defence when the attack comes.
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The FDA uncovered "no specific safety concerns" or allergic reactions in the Moderna trials. Typical reactions included temporary fever, fatigue and aches, especially after the second dose as the vaccine revs up the immune system. These are similar to the reactions seen in Pfizer's vaccine. About 1.5% of vaccine recipients reported possible "hypersensitivity".The Moderna vaccine was more than 94% effective overall at preventing COVID-19 illness, and 86% effective in people 65 and older.
Moderna's safety data is based on an interim analysis of approximately 30,350 participants over 18 years of age randomised 1:1 to vaccine or placebo with a median of 7 weeks of follow-up after the second dose.