In a five-minute video posted to his Twitter account on Wednesday, President Trump stood in entrance of the White House and supplied a lavish endorsement for a remedy he had obtained whereas hospitalized at Walter Reed National Military Medical Center.
“They gave me Regeneron, and it was like, unbelievable — I felt good immediately,” he stated, referring to an experimental cocktail of monoclonal antibodies produced by the pharmaceutical firm Regeneron. “I want everybody to be given the same treatment as your president.”
The president’s video raised many questions, together with whether or not the antibody cocktail may have such a big impact in such a short while. (Some physicians have been skeptical.)
But for the query of how he deliberate to make sure that a remedy not but accepted by the Food and Drug Administration would quickly be obtainable, he had a solution: “I have emergency-use authorization all set,” he stated within the video. “And we’ve got to get it signed now.”
Vaccines, medicine and medical gadgets bought within the United States usually require F.D.A. approval. But for greater than 15 years, the company has had the authority, when sure situations are met, to grant emergency-use authorizations, which permit the sale of unapproved medical merchandise.
It has used such authorizations throughout a number of illness outbreaks, together with H1N1 flu in 2009 and Zika in 2016, however the coronavirus has introduced their deployment on a brand new scale.
Since February, the company has granted greater than 300 Covid-related emergency-use authorizations, and lots of observers count on that Covid vaccines will first be made obtainable within the United States underneath a such a process.