Wednesday, November 20, 2024 6:38:56 PM
DocLee,
I suggest you take a look when the trial was started. We cannot expect to have the matching magnitude like fingerprint as the technology has been evolving with time.
I don't need to mention again about the fact that RevImmune is solely owned by LP.
The most important part is that the DC vaccine as mentioned in the paper had amazing efficacy on the patients with three types of tough cold tumors, which without doubt means DCs can be pulsed with tumor-associated antigens (a lot of them). No other technologies can make DC vaccines pulsed with tumor-associated antigens except the technology owned by NWBO.
If you take a look closely at those authors, can you see any one of them could be the developer of new technology? Would any of them apply for new funding if they developed such an amazing new technology? Would they license the technology to a company for commercialization just like what NCI did to lifileucel?
Again there is no difference in terms of being able to pulse dendritic cells with plenty tumor-associated antigens.
I suggest you take a look when the trial was started. We cannot expect to have the matching magnitude like fingerprint as the technology has been evolving with time.
I don't need to mention again about the fact that RevImmune is solely owned by LP.
The most important part is that the DC vaccine as mentioned in the paper had amazing efficacy on the patients with three types of tough cold tumors, which without doubt means DCs can be pulsed with tumor-associated antigens (a lot of them). No other technologies can make DC vaccines pulsed with tumor-associated antigens except the technology owned by NWBO.
If you take a look closely at those authors, can you see any one of them could be the developer of new technology? Would any of them apply for new funding if they developed such an amazing new technology? Would they license the technology to a company for commercialization just like what NCI did to lifileucel?
Again there is no difference in terms of being able to pulse dendritic cells with plenty tumor-associated antigens.
Recent NWBO News
- Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins As Strategic Adviser To Advance Dendritic Cell Cancer Vaccine Platform • PR Newswire (US) • 04/30/2026 04:38:00 PM
- Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins As Strategic Adviser To Advance Dendritic Cell Cancer Vaccine Platform • PR Newswire (US) • 04/30/2026 04:30:00 PM
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
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- 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
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- Form 8-K - Current report • Edgar (US Regulatory) • 01/15/2026 10:06:20 PM
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- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/28/2025 09:43:27 PM
- 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
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- 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
