Monday, September 26, 2016 4:46:45 PM
Let's look at what we do know and what might happen because of it in the simplest possible scenarios. First we know and big pharma knows that DC treatment potentiates checkpoint inhibitors. These pharmas can either look at NWBO or look for other DCs which may or may not work as well as DCVax in their view. If they skip this approach they would need to experiment with other therapies for use in combinations where safety might be more of an issue. DCVax-L is already a good ways through the path to approval and if Direct moves into registrational status, utilizes optimized endpoints and receives an SPA it might be too. The shotgun approach takes a good deal of time and DC therapies close to approval are very few. If they can get their products used 3× more while perhaps using less product with a better safety profile in a relatively short period of time with potentially 2 types of DC treatment vs having a big question mark in front of them for quite a while, what do you think will make the most sense to their shareholders who also have their own experiences with cancer?
Now is the time that pharma has some leverage with NWBO but if Linda plays hardball and we go into extra innings that leverage will be lost if L is approved before they strike a deal. In most cases, pharma would want better validation but they basically already convinced themselves. Hardball could hurt investors in the short run if potential partners balk at Linda's terms but if NWBO begins monetization without a deal the potential partners could lose in a much bigger way. Their worst case scenario would be if NWBO monetizes and the investigstion finds one or more was found to be playing dirty with NWBO. I really hope this is not the case. Best wishes.
Recent NWBO News
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 09/03/2024 08:01:40 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 08/13/2024 08:01:24 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/09/2024 09:06:07 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 08/08/2024 08:30:09 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 08/02/2024 02:42:28 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 07/30/2024 11:49:38 PM
- Biophma Announces Exclusive In License for Dendritic Cell Technology, Sending Shares Higher • AllPennyStocks.com • 06/17/2024 04:40:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 06/04/2024 09:11:16 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 06/03/2024 09:22:55 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 05/22/2024 08:13:36 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 05/10/2024 09:04:57 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) • 03/01/2024 10:04:38 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 12/02/2023 01:31:35 AM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/16/2023 10:11:54 PM
- Epazz, Inc. (OTC Pink: EPAZ) ZenaDrone Demonstration to Defense Departments of UAE and Saudi Arabia • InvestorsHub NewsWire • 11/15/2023 12:19:31 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/09/2023 09:30:39 PM
- Epazz, Inc. (OTC Pink: EPAZ) US Navy Collaboration ZenaDrone 1000 • InvestorsHub NewsWire • 11/09/2023 01:00:34 PM
- Epazz, Inc. (OTC Pink: EPAZ) US Navy Collaboration ZenaDrone 1000 Extreme Weather Demo • InvestorsHub NewsWire • 11/07/2023 12:29:43 PM
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Integrated Ventures, Inc Announces Strategic Partnership For GLP-1 (Semaglutide) Procurement Through MedWell USA, LLC. • INTV • Sep 24, 2024 8:45 AM