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Friday, January 31, 2014 9:18:50 AM
THe thing to focus on is this: NNVC has known all along what the toxicology requirements are even though not all of us have. They'll have included the knowledge in their calculations and projections. So there is no reason to expect that to change because we suddenly became aware of something they will have know of all along.
If the company is willing to risk wasted a little money (in the very unlikely event that tox tests in one species turn up a problem that would have prevented doing the tests in the others) I see no reason at all why the testing could not be done simultaneously in all three species. I strongly suspect that they are planning on doing exactly that. THe FDA is only concerned with protecting humans, not lab animals.
I know of no reason why they would have to be done sequentially. What the FDA wants out of it is the data and the data will be exactly the same whether the tests are done simultaneously or sequentially.
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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