Saturday, March 29, 2025 12:35:34 PM
xkr,
You’re actually highlighting the beauty of the Roswell deal—time⏱️…
The most exciting aspect of acquiring the Roswell DC platform is that we are already years into its development and clinical investigation as a combo agent. When the NWBO press release was published, we were already in PII which took years to achieve!
When the news quoted and linked below was first published in 2020, the ongoing DC trials had not even started yet. Today, we know that the Phase I Roswell trials were successful and advanced to Phase II, with funding that includes peer-reviewed U.S. government grants.
The trials at Roswell resulted from peer-reviewed research that also took years …NWBO was quite fortunate to acquire the Roswell DC platform at Phase II, and those trials involve more than one distinct type of cancer too!
“Our approach overcame both primary, or initial, and acquired resistance, and we also saw evidence of tumor-specific systemic immunological memory, suggesting that this strategy may generate long-term anticancer responses even against hard-to-treat melanoma and breast tumors.”
https://www.broadcastmed.com/cancer/9753/news/new-roswell-park-strategy-for-overcoming-resistance-to-immunotherapy-unleashes-power-of-dendritic-cells
https://www.nature.com/articles/s41467-020-19192-z
Jump ahead a few YEARS from that 2020 headline and see where we are now with the Roswell DC platform …
https://clinicaltrials.gov/study/NCT04348747?a=15&b=29
https://clinicaltrials.gov/study/NCT04093323?a=39
https://www.prnewswire.com/news-releases/northwest-biotherapeutics-announces-exclusive-in-license-of-portfolio-of-dendritic-cell-technology-and-intellectual-property-302174237.html
I would argue that all scientific and regulatory milestones relevant to “cancer treatment” will swiftly become relevant for investors. The ‘Health & Wealth’ NWBO investment rationale is grounded in science and clinical data, which will ultimately outweigh OTC market manipulation as more data emerge and more peer-reviewed analyses further validate the crucial role DC platforms may play in developing targeted, less toxic combination therapies as SoC for a range of diseases.
While I’m not an expert in the pharma industry or any financial or medical field—and I don’t make specific predictions—I would suggest that there is evidence supporting the expectation of multiple catalysts unfolding in swift succession, rather than just one, such as the MHRA decision…
I’d direct your attention to page 28 of the recent SEC filing. The full document is publicly available, and anyone can access it directly on the SEC.gov site.
The significance of the “contract” references relates to combination therapies, which arguably may be the most meaningful aspect of NWBO from a shareholder perspective (speaking as a shareholder myself).
Currently, we already know that two of the novel platform technologies owned by NWBO are in combo trials at UCLA and at Roswell Park. The combo trials include Merck’s pembrolizumab, the studies have reached PII, interim efficacy data are beginning to emerge, and the three combo studies (one at UCLA and two at Roswell) are supported by continuing peer-reviewed grants awarded by the U.S. NIH and the U.S. DoD.
The references to “contracts” in the10-Q are particularly intriguing, considering what we already know, and we can reasonably expect further details to emerge. Given that these references appear in an official SEC filing, they are factual statements, suggesting that significant news may be forthcoming.
https://www.sec.gov/ix?doc=/Archives/edgar/data/1072379/000141057824001879/nwbo-20240930x10q.htm
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=175992369
You’re actually highlighting the beauty of the Roswell deal—time⏱️…
The most exciting aspect of acquiring the Roswell DC platform is that we are already years into its development and clinical investigation as a combo agent. When the NWBO press release was published, we were already in PII which took years to achieve!
When the news quoted and linked below was first published in 2020, the ongoing DC trials had not even started yet. Today, we know that the Phase I Roswell trials were successful and advanced to Phase II, with funding that includes peer-reviewed U.S. government grants.
The trials at Roswell resulted from peer-reviewed research that also took years …NWBO was quite fortunate to acquire the Roswell DC platform at Phase II, and those trials involve more than one distinct type of cancer too!
“Our approach overcame both primary, or initial, and acquired resistance, and we also saw evidence of tumor-specific systemic immunological memory, suggesting that this strategy may generate long-term anticancer responses even against hard-to-treat melanoma and breast tumors.”
https://www.broadcastmed.com/cancer/9753/news/new-roswell-park-strategy-for-overcoming-resistance-to-immunotherapy-unleashes-power-of-dendritic-cells
https://www.nature.com/articles/s41467-020-19192-z
Jump ahead a few YEARS from that 2020 headline and see where we are now with the Roswell DC platform …
https://clinicaltrials.gov/study/NCT04348747?a=15&b=29
https://clinicaltrials.gov/study/NCT04093323?a=39
https://www.prnewswire.com/news-releases/northwest-biotherapeutics-announces-exclusive-in-license-of-portfolio-of-dendritic-cell-technology-and-intellectual-property-302174237.html
I would argue that all scientific and regulatory milestones relevant to “cancer treatment” will swiftly become relevant for investors. The ‘Health & Wealth’ NWBO investment rationale is grounded in science and clinical data, which will ultimately outweigh OTC market manipulation as more data emerge and more peer-reviewed analyses further validate the crucial role DC platforms may play in developing targeted, less toxic combination therapies as SoC for a range of diseases.
While I’m not an expert in the pharma industry or any financial or medical field—and I don’t make specific predictions—I would suggest that there is evidence supporting the expectation of multiple catalysts unfolding in swift succession, rather than just one, such as the MHRA decision…
I’d direct your attention to page 28 of the recent SEC filing. The full document is publicly available, and anyone can access it directly on the SEC.gov site.
The significance of the “contract” references relates to combination therapies, which arguably may be the most meaningful aspect of NWBO from a shareholder perspective (speaking as a shareholder myself).
Currently, we already know that two of the novel platform technologies owned by NWBO are in combo trials at UCLA and at Roswell Park. The combo trials include Merck’s pembrolizumab, the studies have reached PII, interim efficacy data are beginning to emerge, and the three combo studies (one at UCLA and two at Roswell) are supported by continuing peer-reviewed grants awarded by the U.S. NIH and the U.S. DoD.
The references to “contracts” in the10-Q are particularly intriguing, considering what we already know, and we can reasonably expect further details to emerge. Given that these references appear in an official SEC filing, they are factual statements, suggesting that significant news may be forthcoming.
https://www.sec.gov/ix?doc=/Archives/edgar/data/1072379/000141057824001879/nwbo-20240930x10q.htm
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=175992369
Bullish
Believe carefully. This is the greatest and most powerful lesson that I have learned since arriving on Earth. Examine what you believe about yourself most importantly, and then believe carefully as you interact with the world.
Recent NWBO News
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 04/16/2026 09:25:30 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/07/2026 04:30:50 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) • 03/31/2026 09:04:37 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/15/2026 10:06:20 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/02/2026 10:14:59 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/28/2025 09:43:27 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 11/26/2025 05:15:34 AM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/25/2025 10:23:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/20/2025 09:26:03 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 11/19/2025 09:15:48 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:44:21 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/31/2025 04:29:10 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/30/2025 08:40:05 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/24/2025 04:28:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/14/2025 06:22:26 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2025 09:00:38 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 07/01/2025 09:04:38 PM
