Gilead Sciences’ (NASDAQ:GILD) coronavirus-fighting drug will be in the hands of doctors and patients as early as this week, the biotechnology company’s CEO said Sunday.
“We intend to get [remdesivir] to patients in the early part of this next week, beginning to work with the government which will determine which cities are most vulnerable and where the patients are that need this medicine,” Gilead Sciences chairman and CEO Daniel O’Day told CBS’ “Face of the Nation.”
The scourge has caused unprecedented societal and financial disruption in the U.S. and worldwide. Gilead’s antiviral drug — remdesivir — has been a source of hope for the more than 1.1 million Americans diagnosed with the fast-spreading illness as well as market participants hoping for a swift reopening of the economy.
Gilead released preliminary results from its clinical trial on its antiviral drug remdesivir last week, showing at least 50% of the COVID-19 patients treated with a five-day dosage of the drug improved.
The National Institute of Allergy and Infectious Diseases then released a study that showed COVID-19 patients who took remdesivir usually recovered after 11 days, four days faster than those who didn’t take the drug.
Following these successful trials, the Food and Drug Administration granted emergency use authorization for the drug to treat COVID-19.
That means the drug has not undergone the same review as FDA-approved treatments, but doctors will be allowed to administer remdesivir to patients hospitalized with the disease. All of the drug supply will go to the government to allocate around the nation.
GILD shares dropped 42 cents to $79.52.