Friday, January 11, 2013 4:24:31 PM
Did I ever say that it did? So what? -- most new drugs these days don't come about by accident.
"It is not made in a chemisty lab and not in an industrial factory and is made by medical doctors after years of research in a special laboratory."
Fluicide is made in a bio-chemistry lab just like all those other drugs. Its inventors are doctors and PhDs, just like for all those other drugs. They are attempting to scale up production by - gasp! -- making it in a factory in Connecticut. Sorry, fluicide isn't that special -- it's a drug with a different mode of action than other drugs, but it's still a drug. You look at its unique mode of action and say Fluicide must be much safer than other drugs. The FDA will agree that its mode of action is unique, and that it's entirely different from any other drug that's been tried in humans. For precisely that reason I'm sure they'll be even more demanding than usual of data for safety in humans. It will cost money to meet those demands.
"Over 3500 tests in animals shows no or little toxicity."
You could have said the same thing about methanol.
"The formulas of FLUCIDE are intended to go after the VIRUSes and not the host. Only the viruses will be affected."
Intention and reality are two different things. We won't know that it doesn't have any deleterious effects on humans until we test it on humans.
"Any toxic assertions are assertions only at this time."
Any safety assertions are only assertions at this time.
All your hand waving and special pleading can not change the underlying reality. The safety and efficacy of Fluicide must be tested, and with the same arduous and expensive procedures as are used for other drugs. Investors are holding back because they can add up the numbers, and are wondering just how many more dilutions of shares have to take place before profitability is reached, especially after they take into account that NNVC never meets its deadlines.
Recent NNVC News
- NanoViricides Reports that the Phase I NV-387 Clinical Trial is Completed Successfully and Data Lock is Expected Soon • InvestorsHub NewsWire • 05/02/2024 02:07:42 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 02/16/2024 09:53:32 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/14/2024 09:55:35 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/19/2024 09:44:48 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 12/04/2023 09:08:49 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 10/13/2023 08:30:41 PM
- Form NT 10-K - Notification of inability to timely file Form 10-K 405, 10-K, 10-KSB 405, 10-KSB, 10-KT, or 10-KT405 • Edgar (US Regulatory) • 09/28/2023 08:44:54 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 09/01/2023 08:46:45 PM
- Clinical Trial of Broad-Spectrum Antiviral Drug NV-CoV-2 is Progressing Well, Says NanoViricides - NV-CoV-2 is Positioned to Fulfill Many Unmet Medical Needs • InvestorsHub NewsWire • 07/06/2023 03:16:37 PM
Last Shot Hydration Drink Announced as Official Sponsor of Red River Athletic Conference • EQLB • Jun 20, 2024 2:38 PM
ATWEC Announces Major Acquisition and Lays Out Strategic Growth Plans • ATWT • Jun 20, 2024 7:09 AM
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VAYK Assembling New Management Team for $64 Billion Domestic Market • VAYK • Jun 18, 2024 9:00 AM
Fifty 1 Labs, Inc Announces Acquisition of Drago Knives, LLC • CAFI • Jun 18, 2024 8:45 AM
Hydromer Announces Attainment of ISO 13485 Certification • HYDI • Jun 17, 2024 9:22 AM