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FDA committee votes unanimously, says advantages of J&J’s COVID-19 vaccine outweigh the dangers


Shares of Johnson & Johnson had been up 1.3% in after-hours buying and selling on Friday after a Meals and Drug Administration advisory committee vote 22-Zero in favor of the regulator authorizing the corporate’s COVID-19 vaccine candidate. The FDA just isn’t required to observe the recommendation of the committee however usually does. The one-dose vaccine had an general efficacy charge of about 66% within the Part Three medical trial, and the U.S. arm of the trial confirmed an efficacy charge of about 72% and of 85% when defending in opposition to extreme or vital illness. The commonest opposed occasions had been ache on the injection website and fatigue. The trial was performed within the U.S., South Africa, and a number of other Central and South American international locations. If the FDA strikes ahead with authorizing the experimental vaccine, will probably be the third COVID-19 vaccine to be obtainable within the U.S. – and the primary to require just one dose. Each the Moderna Inc. and BioNTech SE and Pfizer Inc.’s vaccines, which had been individually licensed in December, require two doses spaced a number of weeks aside. J&J’s inventory has gained 10.7% over the previous 12 months, whereas the broader S&P 500 is up 22.4percentMarket Pulse Tales are Fast-fire, brief information bursts on shares and markets as they transfer. Go to MarketWatch.com for extra data on this information.

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2021-02-26



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