The daily business briefing: December 18, 2020

FDA panel recommends Moderna vaccine approval, states sue Google over "search-related monopolies," and more

The Moderna vaccine
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1. FDA panel recommends emergency approval of Moderna vaccine

A Food and Drug Administration advisory panel on Thursday recommended authorizing emergency use of Moderna's coronavirus vaccine. The 20-0 vote, with one abstention, cleared the way for FDA approval, which is expected on Friday. Moderna's late-phase trials concluded that the two-dose vaccine was 94 percent effective. "The evidence for the vaccine highly outweighs any issues that we have seen," said panel member Hayley Gans, a Stanford University pediatrics professor. Moderna's vaccine will be the second to receive emergency approval. A campaign to administer the vaccine made by Pfizer and its German partner, BioNTech, began this week. Moderna expects this month to deliver 20 million doses of its vaccine, which doesn't require special freezers like Pfizer's.

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Harold Maass, The Week US

Harold Maass is a contributing editor at The Week. He has been writing for The Week since the 2001 debut of the U.S. print edition and served as editor of TheWeek.com when it launched in 2008. Harold started his career as a newspaper reporter in South Florida and Haiti. He has previously worked for a variety of news outlets, including The Miami Herald, ABC News and Fox News, and for several years wrote a daily roundup of financial news for The Week and Yahoo Finance.