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Re: None

Tuesday, 01/08/2019 9:49:44 PM

Tuesday, January 08, 2019 9:49:44 PM

Post# of 44784
So, let me get this straight. After all that time spent working with the DOD and BARDA, after all that time radiating and analyzing monkeys, we are going to have to start a phase 1 trial like any other FDA approval process. Great job, guys.

And since this trial is recruiting patients that have been accidentally exposed to radiation as opposed to chemo patients, we could be waiting a very long time. And hopefully we are (meaning I don’t wish anyone be accidentally radiated)!

No doubt I am missing something, but how has any step taken in this R18 process, including this new trial, been “efficient”.. by any possible stretch of the imagination? This seems like them saying “well kids, we fed you BS for years that you in turn fed to your shareholders, buuuut you’re gonna have to start at square one.”