WASHINGTON (Reuters): Moderna Inc will apply for US and European emergency authorisation for its Covid-19 vaccine on Monday (Nov 30) after full results from a late-stage study showed it was 94.1% effective with no serious safety concerns, the company said.
Moderna also reported that its vaccine's efficacy rate was consistent across age, race, ethnicity and gender demographics as well as having a 100% success rate in preventing severe cases of a disease that has killed nearly 1.5 million people.
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