Sunday, October 05, 2014 12:35:54 AM
Yes everyone has an opinion, and the collective opinion of investors is what determines the market cap. Right now, NNVC hasn't shown enough for investors to really buy the story. It remains a great story, if they can start to deliver. I agree that right now, they haven't delivered all that much, just slow and steady progress towards their goals - getting the cides into humans to show they are safe and effective. What's one more year to wait for this incredible potential?
Yes, if it takes one more year I will be surprised. I think things are going to burst in about a month- or less.
I expect a few stages in the rocket launch. First, when the contract is signed with the lab for EBOLACIDE.
Next when preliminary results of that testing surface.
Next when it is clear that the first sample sent to tox studies for FLUcide is followed by a second and third and so on, showing their capacity to produce flucide samples is robust.
Fourth as the EBOLAcide starts showing real promise and the world turns their eyes on Sheldon, Connecticut
and Finally, when Ebolacide is clearly proven to be successful in animals, primates, and humans.
Then, of course, flu season hits with a vengeance... and on and on it goes.
Too good to be true- maybe. But then, maybe not. Also, too bad to be true- unfortunately, for those in the trouble spots.
Recent NNVC News
- Deadly Measles Cases Accentuate the Need for a Treatment - NV-387 is Here to Help Patients and Control Spread, Says NanoViricides • ACCESS Newswire • 04/21/2026 12:30:00 PM
- Measles Rare Pediatric Disease Drug Designation Application Filed for NV-387, PRV Provides for Strong Business Case, Says NanoViricides • ACCESS Newswire • 04/07/2026 12:30:00 PM
- Phase II Clinical Trial of Monkeypox Treatment by NV-387 to Commence Soon, Announces NanoViricides • ACCESS Newswire • 04/01/2026 12:30:00 PM
- NanoViricides Presenting at NIBA's 152nd Investment Conference in Fort Lauderdale, FL March 12, 2026 - Announces Manufacture of Phase II Clinical Product NV-387 Oral Gummies is Complete • ACCESS Newswire • 03/11/2026 12:30:00 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 02/17/2026 09:30:47 PM
- MPox Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/12/2026 01:30:00 PM
- Measles Orphan Drug Designation Application Filed for NV-387, Declares NanoViricides • ACCESS Newswire • 02/10/2026 01:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 12/30/2025 09:30:18 PM
- Form DEL AM - Delaying amendment • Edgar (US Regulatory) • 12/16/2025 09:30:05 PM
- Form S-3 - Registration statement under Securities Act of 1933 • Edgar (US Regulatory) • 12/15/2025 09:26:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/26/2025 09:30:33 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:32:10 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 07:54:28 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/12/2025 04:29:54 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/01/2025 09:07:54 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 09/29/2025 08:33:17 PM
