You are citing the FDA rule/regulations. Fine. Should FDA allow toxic Cannabis go to market without clinical trials? The law/regulations should apply equally to all companies. Why the exception, the double-standard, with toxic Cannabis? We are a small biotech company with low toxicity, fast acting, effective nanoviricides. Six thousand animal subjects survived lethal doses viruses like Influenza, Dengue, etc., thanks to nanoviricides.
Why does the FDA put hurdles on our small biotech company??? Why find the toxic dose? FDA could have requested the toxic dose for later and that would have been ok. All of this while you see vaccine makers getting all kinds of taxpayers money and I am referring to big cap companies in comparison to our small biotech. And how generous of some companies/governments to donate vaccine doses that were made possible/manufactured with taxpayers money. It is as if they were saying, "...use those vaccine doses quickly because if the virus mutates they will become worthless...". And whatever happened with Tamiflu data? Billions were spent by governments just to find out later that the vaccine was marginally effective.
The PEG molecule is common to all nanoviricides, yes? The difference among nanoviricides What products are out there in the market with PEG that have been, by FDA regulations, required to undergo clinical studies. What were their results and are they in the market today? Perhaps it may be easier to cite the failures, if any.
If EbolaCide tests in BSL-4 facility and if found to be highly efficient, why not employ it right away to fight Ebola? How far did Zmapp go, in meeting goals according to FDA regulations, before it was employed in the US and in Liberia, Africa?
If we are not delayed for FluCide, we are not delayed for 2015. Why would any one say "not delayed" and skip the entire 2015? You said it in one of your posts, time will wait for no one, not even NNVC.
Thirteen weeks (13 weeks)? We are advancing with FluCide in paralell to EbolaCide. Are FluCide GLP full tox studies worth anything in relation to EbolaCide and FDA regulations/requirements?
I don't have the time to post any other questions this morning. Perhaps in the evening.
