An Emergency Use Authorization was granted for the Regeneron antibody cocktail by the FDA yesterday, as expected (and slightly surprised it was granted later than Lilly's EUA for their antibody treatment which does not look as effective). Both the Lilly and Regeneron monoclonal antibody treatments are for mild/moderately ill COVID patients prior to hospitalization, where they've had good clinical trial results, so far (especially the Regeneron one).
https://www.cnn.com/2020/11/21/health/regeneron-fda-clearance-trump-coronavirus/index.html
"Regeneron now expects to have REGEN-COV2 treatment doses ready for approximately 80,000 patients by the end of November, approximately 200,000 patients by the first week of January, and approximately 300,000 patients in total by the end of January 2021," the company said in their news release yesterday.
This is a start, but only a start, given that we're almost seeing 200,000 cases per day now - these monoclonal antibody drugs will be reserved for elderly patients and those with high risk factors (like Trump and Christie, who both received the Regeneron treatment). Unfortunately, the Regeneron cocktail clinical trial was put on hold for patients on ventilators and those receiving supplemental oxygen - many (including me) had hoped it would work as well in seriously ill patients.
https://investor.regeneron.com/news...cov2-first-antibody-cocktail-covid-19-receive