Sunday, August 28, 2016 3:11:52 AM
The absolute best we can hope for:
1. NNVC does in fact select a candidate for ocular Herpescide by the end of this year. That is all they expect to accomplish according to their SEC filings. And of course NNVC has never yet met any of their own time tables. So far we have no indication that any samples have even gone out to any of the universities doing the testing, so this optimistic time table requires that an awful lot be done in the next four months after 8 months of no discernable progress.
2. Then the best we can hope for is that NNVC somehow gets tox done before 2017 is over. Remember that in 2014 it took a full year to make 200g of Flucide (nowhere near enough to complete tox) and then do the little bit of tox testing that could be done with that 200g. So I say one full year to get Herpescide tox done. Minimum.
3. So, we will be at the end of 2017 with no clinical trials in sight. But wait -- NNVC can't do clinical trials until it gets IND approval from the FDA. Figure at least 6 months for this -- it involves the federal government.
So, like I said, no clinical trials for Herpescide in 2016 or 2017. Bank on it. There's a very good chance that there will be no clinical trials in 2018, either, as NNVC typically misses its time tables by factors of 2 or more.
1. NNVC does in fact select a candidate for ocular Herpescide by the end of this year. That is all they expect to accomplish according to their SEC filings. And of course NNVC has never yet met any of their own time tables. So far we have no indication that any samples have even gone out to any of the universities doing the testing, so this optimistic time table requires that an awful lot be done in the next four months after 8 months of no discernable progress.
2. Then the best we can hope for is that NNVC somehow gets tox done before 2017 is over. Remember that in 2014 it took a full year to make 200g of Flucide (nowhere near enough to complete tox) and then do the little bit of tox testing that could be done with that 200g. So I say one full year to get Herpescide tox done. Minimum.
3. So, we will be at the end of 2017 with no clinical trials in sight. But wait -- NNVC can't do clinical trials until it gets IND approval from the FDA. Figure at least 6 months for this -- it involves the federal government.
So, like I said, no clinical trials for Herpescide in 2016 or 2017. Bank on it. There's a very good chance that there will be no clinical trials in 2018, either, as NNVC typically misses its time tables by factors of 2 or more.
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
