Wednesday, June 18, 2025 12:05:47 AM
I understand just as much as you by reading your earlier posts, not an expert by any means but spent more time on it than I would have liked.
I can write whatever I want as long as I don't brake forum rules, dude, so I suggest you get down from your high horse, you fanboys are just incredible!
The company is diluting all shareholder's worth into nothing, you have to buy about 20% of your share count each year, in order to maintain your % of the company! I refuse to do that, I am done buying as much as a single share more.
Why are the company presenting new data from an old P1 trial? And D not L? Odd man. They should be concentrating about getting L over the line instead.
Why is that approval dragging out for such a long time, I don't believe it's manufacturing as some hinted.
The links I posted got me even more worried, Google don't seem to "know" anything about NWBO and DC-Vax.
Why are Harvard and Yale concentrating about developing new personalized cancer vaccines when we got DC-Vax, Huh? They are maybe not interested and think they can make something that's better or Linda P is impossible to work with (no partners over all those years!)? It can only be one of the 3, so which is it?
FDA's new rapid approval politics could move them very quickly forward, not spending decades on it.
I come to realize that my investment here is maybe lost. If I sell now, I'II get less than 1/2 of my investment back, LOL, so I stay until approval or refusal.
Thankfully, my investments are spread out so I can walk away with my shirt on.
I can write whatever I want as long as I don't brake forum rules, dude, so I suggest you get down from your high horse, you fanboys are just incredible!
The company is diluting all shareholder's worth into nothing, you have to buy about 20% of your share count each year, in order to maintain your % of the company! I refuse to do that, I am done buying as much as a single share more.
Why are the company presenting new data from an old P1 trial? And D not L? Odd man. They should be concentrating about getting L over the line instead.
Why is that approval dragging out for such a long time, I don't believe it's manufacturing as some hinted.
The links I posted got me even more worried, Google don't seem to "know" anything about NWBO and DC-Vax.
Why are Harvard and Yale concentrating about developing new personalized cancer vaccines when we got DC-Vax, Huh? They are maybe not interested and think they can make something that's better or Linda P is impossible to work with (no partners over all those years!)? It can only be one of the 3, so which is it?
FDA's new rapid approval politics could move them very quickly forward, not spending decades on it.
I come to realize that my investment here is maybe lost. If I sell now, I'II get less than 1/2 of my investment back, LOL, so I stay until approval or refusal.
Thankfully, my investments are spread out so I can walk away with my shirt on.
Recent NWBO News
- CNS Drug Delivery Breakthroughs Unlock Significant Biotech Market Opportunities • InvestorsHub NewsWire • 05/11/2026 01:00:00 PM
- CNS Drug Delivery Breakthroughs Unlock Significant Biotech Market Opportunities • GlobeNewswire Inc. • 05/11/2026 12:30:00 PM
- Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins As Strategic Adviser To Advance Dendritic Cell Cancer Vaccine Platform • PR Newswire (US) • 04/30/2026 04:38:00 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
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 04/21/2026 04:15:08 AM
- 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 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
