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Re: Black-Ops post# 137672

Saturday, 01/02/2021 2:40:48 PM

Saturday, January 02, 2021 2:40:48 PM

Post# of 232568
Question for you...or anyone that wants to chime in

Does the company need to officially submit something for FDA approval following unblinding or does that happen in accordance with primary endpoints being met following completion of the phase 3 trial?

Does the data need to be unblinded before the FDA makes a determination?

I’m trying to understand how covertly this process can be to avoid tipping off investors of what the intentions of the FDA would be
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