Would it be possible for BOT management to seek exemption from a phase iii trial?
Epidiolex already has FDA approval with a CBD active...
and it wouldn't be the first time, Painkiller "Rexista RX" didn't need to go through phase iii because it was deemed "bioequivalent" to the already FDA approved OxyContin.
Thoughts?
Ann: Investor Presentation, page-47
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