Moderna Submits Covid-19 Vaccine For Emergency Approval, Says It Is 100% Effective At Preventing Severe Forms Of Disease

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Moderna will submit its Covid-19 vaccine for emergency use approval in the U.S. Monday after new trial data showed it to be 94% effective at preventing the disease, findings that are consistent withModerna will apply for emergency use approval for its Covid-19 vaccine Monday after promisingNew findings from the Phase 3 clinical trial, which involved over 30,000 participants, showed the vaccine to be 100% effective at preventing severe Covid-19 and 94% at preventing the disease more broadly.

The company says the findings are consistent across various demographics, including age, gender and ethnicity. No serious safety concerns were identified, the company said, with side effects limited to injection site pain, headaches and fatigue. Off the back of the results, and having collected the requisite two months of safety data, Moderna says it will apply for emergency use authorization from the U.S.’s Food and Drug Administration, as well as seek conditional marketing authorization from the European Medicines Agency.Big Number

20 million. That’s the total number of doses that Moderna expects to have ready to ship to the U.S. by the end of 2020, enough for 10 million people to be vaccinated as the vaccine requires two doses. The company says it is on track to manufacture between 500 million to 1 billion doses globally in 2021.Speaking about the results, CEO Stéphane Bancel emphasized the vaccine’s high success rate and, in particular, its ability to prevent severe disease.

 

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Is that claim of 100% chance of reducing cold/flu symptoms? or 100% chance of generating immunity to Covid-19? Definitions matter, especially when it's symptom reduction that the 'vaccines' are being measured against

FDA in December handing out approvals

thank you very much for your work

When it will be available for common public?

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