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Monday, October 10, 2011 4:28:19 PM
Back then the numbers I came up with were based on licensing for manufacture and market, which would net NNVC a royalty ranging anywhere from 10% to 22%, depending on the risk the Big Pharma took in its role in development. Back in the pre-2008 period there were a dozen early licenses signed during animal studies where the development biopharma received more than $100 million and at least a 7% royalty. Contracts after Phase 1 fetch 10% and 15% royalties with late Phase contracts earning significantly higher.
I think NNVC will be looking for a marketing and distribution partner, which means the numbers shift upwards for earnings against gross sales. Emergency and critical care use authorization could run as high as $2000 per course with NNVC netting 40% of that. That would be 200K cases a year for FluCide, and expanding rapidly from there.
Roche paid Gilead 14% to 22% for royalties after licensing to complete the development, human trials, FDA approval and manufacture and marketing for TamiFlu. After emergency use authorization, first year earnings for TamiFlu sales were $1.5 billion against which Gilead earned an average of 19%. Roche had already paid for all development and approval costs since 1996 plus more than a hundred million in benchmark payments, and another $67 million in back payment Royalties for use awarded in late 2005 just before FDA emergency use authorization.
If NNVC hooks up in a similar way, I think earnings even in a royalty structured agreement will be at least as good as Gilead/Roche.
Recent NNVC News
- 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
- 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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