Tuesday, October 08, 2013 9:51:04 AM
If someone can only look at the issue in such generic terms and comes up with such a deeply flawed analysis that they missperceive one of the most positive events that can happen to a drug candidate at this stage [[the toxicity is SO LOW that preliminary tox tests are required. OH< and BTW: there's a strong possibility that the drug may qualify for a FAST TRACK. And the time to the end of clinical trials will be much FASTER]]
Perhaps some are investing in a sector where their understanding is dangerously inadequate.
BTW: the OTHER major qualification for a fast track (other than very low toxicity) is high efficacy, which NNVC's drug also appears to have "in spades".
PS!!! Also note that getting a "fast track" very greatly speeds up the process of clinical trials IN ADDITION to all the other factors. (shouldn't have to point that out, but considering past posts .....)
Recent NNVC News
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 09/27/2024 08:15:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/09/2024 08:30:39 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 08/09/2024 08:05:25 PM
- 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
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