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Wednesday, May 16, 2012 12:59:23 PM
The following steps have to take place:
1. The necessary toxicity studies have to be completed and the IND must be approved by the FDA.
2. Phase I trials have to be carried out. They have to be successful (no significant toxicity in humans).
3. The FDA has to approve Phase II or combined Phase II/III trials.
4. NNVC must raise enough money to carry out these far more expensive trials. That means more dilution of shares.
5. The trials have to actually cure the flu in human beings. We all hope this will be the case, but nobody knows whether it will work as of now.
6. The FDA has to approve the drug.
My most optimistic timeline is that it will be 2 years before NNVC has any drug curing any human disease, with 3 years being more likely. That assumes that the basic technology is sound, and will actually cure viral diseases in humans.
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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