The FDA Strongly Hit I meant to imply that a scan

The FDA Strongly Hit
I meant to imply that a scandal may arise, involving remdesivir, plasma and the FDA possibly kicking Cytodyn aside. Favoring BP? Thus, the FDA could been accused of approving moderate efficacy drugs, while ignoring powerful efficacy drugs, which thus, would have allowed hundreds of thousands to die. A conservative response will be "we must trust the system of Clinical Trials and not deviate, deviation from FDA trial protocol is dangerous ground. Let the FDA and the trials do their approval process, it takes time, we must remain patient". (and 5 months afrer May 31, still 800 to 1000 die/day in the US, we are well over a million dead on the planet).
At the end of May, Dr Patterson had spoken to the world, bottom line stating that LL could cure covid-19. Coincidence about that same time, the FDA ending our eIND trials, which showed compelling evidence of LL efficacy, Dr P claimed zero viral load in I think 60 out of not sure 65 or 68 s/c patients. The FDA should have at least continued our eIND, and possibly then later, after more "compelling results", adapted something, adapt some of their protocol, to allow LL to be accessed. How many have died on the planet since May 31? Now still, great m/m Top Line results, but no EUA for m/m.
"Probably" great Interim s/c results, crisis gets worse on the planet, some hospitals overwhelmed, shutdowns, evictions, foreclosure and bankruptcies
increasing, but no EUA for LL s/c. Wait 2 or 4 months?????