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A panel of the Food and Drug Administration meets Thursday to vote on whether to recommend approval of Moderna’s coronavirus vaccine for emergency use.
Before the vote, which is expected to take place at the end of the day, the Agency’s Advisory Committee on Vaccines and Related Biological Products will review and discuss Moderna clinical trial data and provide its opinion on the vaccine, including whether the benefits are the risks for a vaccine, emergency approval predominates.
The FDA is not required to follow the advice of the advisory group, but it often does.
A positive vote from the committee will likely pave the way for the FDA to approve Moderna’s emergency vaccine. It would be the second to be approved for use in the US after Pfizer’s vaccine.
The all-day meeting takes place from 9 a.m. to 5.15 p.m.
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