Friday, March 05, 2010 6:54:48 PM
It's a nest egg - to hatch when needed, I guess. Although they said at one point recently (Seymour at that conference on the web - I listened) that financing was a serious endeavour-concern for them and was something to be discussed with participants there in private sessions. Seymour has said recently that money is needed, and is holding up progress if I read him rightly. Now who needs the financiers? I'm not sure if they are to be in the picture or not - methinks this public funding says, to me, the financiers are not needed. But if more than $40 million is needed then I suppose they might be in the picture or another shelf is needed. Could be the financiers will buy a tranche of shares and sell them or keep them depending on circumstances but we get the $40 million or part thereof to use as needed.
In figuring out the amount needed for this shelf I imagine that they figured what would be appropriate for the near future for various eventualities and this is what they came up with. I would have gone for MORE! Never hurts to show you mean business. And yet again they have said all along and quite recently that the plan is and always has been to involve big pharmas in distribution and manufacture. I have seen other startups that get big pharma footing the bill early on in the FDA process. Are we different? Could be. How? All I can think is that what we offer is miles above what these other startups are offering. If I had my druthers, I'd involve big pharma to suit US (!!) and go into manufacture as well to supply the market we keep to ourselves. Leave what we do not want to serve to big pharma and keep the rest and best for US. Dengue, for example - keep that for us (and Eva!!) exclusively and supply the market worldwide. For EKC, involve big pharma - a pick and choose approach. That way we gain the experience and GROW. Does that make sense? Alls I'm trying to do is make sense out of this $40 million. No money in Dengue? Ask those countries like Sri Lanka and Malasia and Indonesia what they think it is worth!
In figuring out the amount needed for this shelf I imagine that they figured what would be appropriate for the near future for various eventualities and this is what they came up with. I would have gone for MORE! Never hurts to show you mean business. And yet again they have said all along and quite recently that the plan is and always has been to involve big pharmas in distribution and manufacture. I have seen other startups that get big pharma footing the bill early on in the FDA process. Are we different? Could be. How? All I can think is that what we offer is miles above what these other startups are offering. If I had my druthers, I'd involve big pharma to suit US (!!) and go into manufacture as well to supply the market we keep to ourselves. Leave what we do not want to serve to big pharma and keep the rest and best for US. Dengue, for example - keep that for us (and Eva!!) exclusively and supply the market worldwide. For EKC, involve big pharma - a pick and choose approach. That way we gain the experience and GROW. Does that make sense? Alls I'm trying to do is make sense out of this $40 million. No money in Dengue? Ask those countries like Sri Lanka and Malasia and Indonesia what they think it is worth!
Recent NNVC News
- 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

