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Thursday, 03/11/2021 12:34:55 PM

Thursday, March 11, 2021 12:34:55 PM

Post# of 233055
FDA knows LL works! Otherwise they would have shut down EIND last week for severe to critical COVID patients, and not approved ph2 for LH studies. Perhaps no one at the FDA wants to stick their neck out for a small biotech firm (and perhaps set a precedence), but deep within they know very well that the drug works as intended. Therefore, they are asking CYDY to run a quick 140 patient trial with critical patients, which everyone knows will be a home run! Would they have taken a similar approach with big pharma (say a Gilead, Pfizer, J&J)? No, and that's what is painful - their double standards. It's unfortunate, but credibility and money influences a lot of decision making than real data points!

Silver lining for us, once we hit EUA on COVID critical patients in 3 months, sky is the limit! Until then we get back to around $5?
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