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Friday, March 06, 2020 2:45:32 PM
1) NNVC doesn't actually have a license from Diwan/Theracour to produce a medicine for this virus or group of viruses at this stage,... and that would have to be 'negotiated' in some way.
2) NNVC doesn't have any actual test data - model organism or otherwise - of which we are aware that indicates that their proposed medicine does anything useful,... so they would have to spend a year or more generating some actual data.
3) NNVC doesn't have any toxicity testing data for an ingested or injected version of any of their drugs,... so they would have to first make enough quantity (this capability is debatable of course) to do toxicity testing and then do the testing.
4) Aren't they actually supposed to be working on clinical testing for their topical anti-shingles treatment currently?
Just because you can doesn't mean you should.
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
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