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Re: BonelessCat post# 45757

Wednesday, 02/16/2011 6:39:49 PM

Wednesday, February 16, 2011 6:39:49 PM

Post# of 146240
Wrong again. You have to have standardized some kind of GLP supply, put that into toxicology studies, and then file an IND. They have done none of that. You can't do home-brew mock-up drug supply and show it to the FDA and expect toxicology will be done.


NNVC should set the expectation for an IND for 2012 at best.

Simplest question for management is, do you have GLP clinical supplies? If so, which drug candidate?
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