But here's what I don't understand -- why would th

But here's what I don't understand -- why would the FDA have allowed Leronlimab to be used for 30 or so EIND critically ill patients, if not to hopefully save lives?
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Because the FDA, just any other state agency, must first and foremost cover their behinds. It's a part of the game. Let's suppose the "American public" is something that really exist and even can wage a powerful protest through "free press" which would make TPTB to investigate the FDA's games with CYDY. The agency then will have the irrefutable evidence of its good will, nay, its eagerness to go an extra mile for the sake of the American people. They allowed Leron as many COVID-19 EINDs as were requested. They speedily approved its two clinical studies for COVID-19. They approved a basket cancer trial and gave other similar goodies to NP. They had approved Leron for the HIV combo! And if all this evidence is still not enough for the American public and FBI, listen to each and every public appearance of Mr. Pourhassan in which he showers our agency with endless praises! Of course, none of the above matters at all! For the FDA, as any other state agency, has up its sleeve the endless number of tricks not to allow the commercialization of any drug that they for whatever reason don't want to succeed. On my short memory of following CYDY they used only one of those tricks when out of the blue they told NP to change the clinical part of BLA just "nine days" before it was ready to be submitted. And this little trick alone has cost us already 4 months and counting. Yep, it will be a lengthy uphill struggle with by no means certain results.

Whatever happens, we have got
Le-Ron-Li-Mab, and they have not.