Its proven efficacy made Moderna’s COVID-19 vaccine to be a few steps away from receiving the EUA
Moderna is just a few steps away from receiving the US Food
and Drug Administration’s emergency use authorization (EUA).
According to insiders,
Moderna’s experimental COVID-19 vaccine meets the requirements, as it is
“highly effective” in preventing the potentially deadly complications caused by
the COVID-19 infection. Moreover, the Administration’s review confirms that the
potential medicine is indeed 94.1% effective.
“The 2-dose vaccination regimen was highly effective in
preventing PCR-confirmed COVID-19 occurring at least 14 days after receipt of
the second dose,” read the FDA’s statement. An official decision will be made
on Thursday and could be available to the public as early as next week.
Following the news, Moderna stock price traded 1.24% higher.
Sources: cnbc.com, thestreet.com
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