The company thinks it could make millions of treatment courses of remdesivir available by the end of the year if it receives FDA approval, the Gilead CEO said.
, is moving very quickly with the FDA for authorization to get the drug to patients, the CEO of the company, Gilead Sciences, said Friday., CEO Daniel O'Day told the"TODAY" show in an exclusive interview.
The company thinks it could make millions of treatment courses available by the end of the year, O'Day said. Its production capacity has already gone from 5,000 treatment courses to 100,000, he said.At the same time, Gilead and the Food and Drug Administration's collaboration"has been terrific" on possible emergency-use authorization for remdesivir as a coronavirus treatment, O'Day said.
"I expect that they're going to act very quickly," O'Day said,"and we’re prepared as a company to make sure we get this medicine to as many patients as possible as soon as possible after that approval."Sign Up
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