With the FDA as the exclusive arbiter of whether C
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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.