(Total Views: 709)
Posted On: 09/29/2022 1:52:30 PM
Post# of 154867
Quote:
With the FDA as the exclusive arbiter of whether CYDY can conduct future trials in Nash and/or cancer, it cannot be assumed that CYDY will ever conduct any trial during the sale period for the 350 million new shares.
I also can't assume you are posting that in good faith. If the FDA blocks Cytodyn when it is presented with good safety data then the FDA is exposing itself to a lawsuit.
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