Trump pushes quick FDA approval of COVID-19 antibody treatments

Both the White House and FDA decreased to comment to the Post..

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The pressure from the president for the FDA to authorize the treatments may make it appear the company is driven by politics, not science, the Post reported.

” Once they provide the [authorization], it will eliminate the trials, and as a society we will have less information moving forward as far as who does it work in, and who to prioritize,” David Boulware, MD, an infectious diseases physician at the University of Minnesota Medical School in Minneapolis, told the Post..

Eli Lilly said it should have about 1 million dosages of its antibody drug by the end of the year..

The president claimed in videos posted on Twitter today that Regenerons drug is a “treatment” for COVID-19 and that it would be broadly readily available soon. Regeneron has actually said that, in the next couple of months, it will have only sufficient supply to deal with the variety of individuals in the U.S. who have become sick in the last week, about 300,000 dosages the Post reported.

Both guys have actually called FDA Commissioner Stephen Hahn in current days to advise him to accelerate the firms evaluation of the drug, two senior administration authorities told the Post..

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Numerous physicians and researchers have actually stated antibody drugs are among the most appealing treatments for COVID-19, however medical trials of the drugs have actually not been completed..

They are likewise promoting Eli Lillys COVID-19 antibody drug, which resembles Regenerons, to receive permission. Both business said today that they have requested emergency situation permissions..

” The fundamental problem with monoclonal antibodies is theres inadequate around the world capacity to produce adequate of them to have a real influence on the disease,” Ezekiel Emanuel, a health policy professional who is encouraging the campaign of Joe Biden, informed the Post. “Yes, they might be great, but for a little number of clients.”.

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Friday, October 9th, 2020
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President Donald Trump and White House Chief of Staff Mark Meadows are both prompting the FDA to rapidly approve an emergency usage permission for Regenerons antibody drug, which the president got as a treatment for COVID-19, The Washington Post reported..