Posted on 11/10/2020 6:21:57 AM PST by RoosterRedux
The U.S. Food and Drug Administration has given Eli Lilly & Co. the first emergency use authorization for its COVID-19 antibody treatment, which the pharmaceutical leader hopes will help infected people avoid hospitalization.
Eli Lillys bamlanivimab therapy will help people 12 and older with mild or moderate coronavirus get a one-time treatment through an IV. The experimental therapy is similar to the treatment President Donald Trump received after contracting the virus last month.
The latest development in COVID vaccine raised Eli Lilly stock by as much as 5.2 percent in late trading on Monday. The Indianapolis-based drugmakers stock had gained 8.3 percent this year.
Eli Lilly antibody treatment to fight COVID-19 David Ricks, Eli Lillys CEO, believes the bamlanivimab therapy is a valuable tool for doctors fighting the now-increasing burden of this global pandemic.
(Excerpt) Read more at industryleadersmagazine.com ...
Right after the election these guys are the worst human beings in American history
The Pandemic will be OVER in a matter of 3-6 moths, over.
Lilly (LLE) and Pfizer (PFE) are both up over 3%+ in premarket trading this morning.
Lilly and Regeneron both have effective antibodies. Pfizer test results show 90% effective inoculation immunity, and Sinopharm has a sample set of 56,000 inoculated with zero cases of infection by people who are traveling internationally. Science won it’s now up to distribution of these preventative and the cures for those already infected. 6 months is a fair timeline for complete saturation of both methods of controlling the China bioweapon which means a year from release to squashing it absolutely historic in success no other pathogen has been neutralized in a time frame even approaching this.
Trump should have won in a landslide on that alone.
What constitutes an emergency? They say it treats mild cases. How can you get this treatment?
You have to get a mild case that is an emergency.
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