In my mind it was a no brainer, we should of gone straight to Europe for the HD PIII. Amazing that they didn't put it to the FDA on the first day. What will it take? To be asked after more than 18 months to supply more data means someone has gone off on their own.
Hopefully something will come of this time in the wilderness and they have designed a better PIII study.
Ann: Prana provides regulatory update for PBT2-PBT.AX, page-4
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