The fda is the arbiter of efficacy, right? And that's why those points are so value accreative at each phase. bioentac was just too small to do it on their own. They didn't have the muscles to run their own big clinical trial and stuff. If you put your investment analysts hat on for a second, thinking about the future, if mederna becomes the next genenta in the next five to ten years, w created that for them.

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