Replies to post #108620 on NanoViricides Inc. (NNVC)

[erdoc1958]

Big K, I recall a post of yours sometime in 2012 or 2013 when you said if NNVC not deep into the FDA approval process by 2014 it would not happen. What do you think now and have you changed your opinion?

[Rawnoc]

BK: Can you explain what you meant when you said:

what you seem to refuse to understand is Human consumption does not need FDA approval; nnvc only needs IND going effective. Of course that's only for the US market. With approval from Uganda's FDA nnvc can do Human use there, among a dozen African nations that are desperate for an HIV antiviral option. This can be accomplished simply by completing the tox package.

Similarly, nnvc working with the help of Dr. Harris could very easily get a clearance for clinical Huanitarian use from any among the dozens of governments under Dengue threat south of the US mainland.

In both cases, nnvc is within a year of Human testing.

What did you mean they only need IND going effective to get human consumption of the codes in the US?

Since there is ZERO focus on either of these 2 previous candidates, and we are years later, is Uganda still looking to do HIVcide testing and Dr. Harris is close to getting clearance from any of the dozens of govt.'s under dengue threat south of the US mainland (are those countries still even under such a threat)?

And is nnvc was within a year of Human testing or is there a new timeline?