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Tuesday, August 10, 2021 2:43:19 PM
Just look at the PR CYDY put out. Notice how Nader/Kelly omitted "stop the trial because no chance of hitting endpoint"? instead THE ONLY SAY "STOP TRIAL BECUASE OF SAFETY" Everyone knows LL is safe which is another red flag for its MOA. Notice how they avoided the DSMC recommendation for second review? They gave a BS response about not following recommendation for time efficiency. Just like Nader claim that the fda not wanting a meeting and instead have a phone call is actually better. They avoided the review from DSMC because then they would have to issue the results that the trial was going to fail ( which it did do to lack of PHase3 in US) AND NOW TRYING FOR EVERY EMERGING MARKET UNDER THE SUN.
https://www.cytodyn.com/newsroom/press-releases/detail/477/cytodyn-receives-positive-dsmc-recommendation-after-interim
Noticed THIS GEM, WHATEVER HAPPEND TO ALL THE BS ABOUT MHRA?
Clinical trial sites in the U.K. are expected to initiate enrollment in the coming days.
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