Some of those may have doubled up but im sure everyone can work it out. The EOP reads as it is, end of phase meeting Q4 which i think it will be the fda telling Alterity what path they can or need to walk next once they have collaberated the full phase 2 results (201-202) which can only be done after phase 2 202 topline data is released mid year . It also states that companies will have multiple meetings with fda in between. Everything seems to be cruising along as it should be without corners being cut as far as I can tell.
my thoughts not yours
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