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Re: FDApproved post# 8046

Wednesday, 11/08/2017 3:46:06 PM

Wednesday, November 08, 2017 3:46:06 PM

Post# of 44784
If they wanted it sooooooo bad like you think, wouldn't it have just been easier to start the trial right after dosing was done. Much easier and way less bureaucracy. But when your ideas don't come to fruition like most times, you switch to some crazy scheme. All one big front to get R18. Just like Lonza theory. LMBO