Gilead's Coronavirus Drug Could Soon Gain Emergency Authorization: Report [Investor's Business Daily]
Gilead Sciences, Inc. (GILD)
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Related news Gilead Sciences ( GILD ) said Wednesday its experimental coronavirus treatment succeeded in a Phase 2 study — leading to suggestions the Food and Drug Administration could grant an emergency authorization for the drug this afternoon. According to the New York Times, the FDA's emergency use authorization for the drug known as remdesivir is imminent. Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said he was "very optimistic" on the study. The NIAID hosted the Phase 2 study. Gilead said the coronavirus treatment met the key goal of that test. The NIAID will reveal that data in an upcoming presentation, Gilead said in a news release. In addition, Gilead said its own Phase 3 study of remdesivir in severe Covid-19 patients showed a similar benefit was seen from a five-day course as for a 10-day regimen. This could expand the number of doses Gilead can make of the coronavirus treatment. Needham analyst Alan Carr called the news encour
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- Gilead Sciences (NASDAQ:GILD) had its price target lowered by analysts at Royal Bank Of Canada from $105.00 to $100.00. They now have a "sector perform" rating on the stock.MarketBeat
- Gilead Sciences (NASDAQ:GILD) had its price target raised by analysts at The Goldman Sachs Group, Inc. from $110.00 to $115.00. They now have a "neutral" rating on the stock.MarketBeat
- Hopping Mad Over Drug Company Product Hopping [Forbes]Forbes
- Gilead Sciences (NASDAQ:GILD) had its "buy" rating reaffirmed by analysts at UBS Group AG.MarketBeat
GILD
Earnings
- 10/30/25 - Beat
GILD
Sec Filings
- 1/16/26 - Form 4
- 1/16/26 - Form 4
- 1/15/26 - Form 144
- GILD's page on the SEC website