Saturday, January 01, 2022 1:21:54 AM
Happy New Year JRIII. I’ll admit that you and others were right when you predicted no TLD in 2021 and I was 100% wrong.
I’m not gonna argue about how the FDA will view the SAP changes, although I agree with Gary.
I’m not sure if you’ve ever experienced first hand what it is like to watch someone you care about suffer and die from GBM. It is an understatement to call it a horrible disease.
Everything about GBM is torture, from the lack of any treatment that works, to the brain trauma and rapid decline, to the horrible side effects of the current SOC, to the hopelessness and helplessness of patients and their families - mothers and fathers, sons and daughters, husbands and wives, brothers and sisters.
I can tell you first hand that my friend who got DCVAX at UCLA is still alive and enjoying life 9 years later, while my stepfather lasted 6 horrific months that I can’t even begin to describe. I’ll just say that we had to lock his doors and hide all the knives in the house because the man we knew was long gone and replaced by an emaciated memoryless wreck with traumatic brain injury who didn’t even recognize his own daughter.
So I respectfully ask that you consider the effects of GBM on millions of lives and the FACT that DCVAX safely extends many peoples lives (OS) far beyond any approved treatment and without any of the horrible side effects.
For the sake of those suffering from this devastating and heartbreaking disease, let’s all hope DCVAX gets approval and quickly.
If it doesn’t based on the use of historical controls due to compassionate crossover of the trial’s original control arm and a reordering of endpoints to address a newly discovered issue of pseudo progression, then it will be be one of the biggest travesties in the history of medicine. The suffering of us investors will pale in comparison to the millions of patients and families that will be destroyed.
I’m not gonna argue about how the FDA will view the SAP changes, although I agree with Gary.
I’m not sure if you’ve ever experienced first hand what it is like to watch someone you care about suffer and die from GBM. It is an understatement to call it a horrible disease.
Everything about GBM is torture, from the lack of any treatment that works, to the brain trauma and rapid decline, to the horrible side effects of the current SOC, to the hopelessness and helplessness of patients and their families - mothers and fathers, sons and daughters, husbands and wives, brothers and sisters.
I can tell you first hand that my friend who got DCVAX at UCLA is still alive and enjoying life 9 years later, while my stepfather lasted 6 horrific months that I can’t even begin to describe. I’ll just say that we had to lock his doors and hide all the knives in the house because the man we knew was long gone and replaced by an emaciated memoryless wreck with traumatic brain injury who didn’t even recognize his own daughter.
So I respectfully ask that you consider the effects of GBM on millions of lives and the FACT that DCVAX safely extends many peoples lives (OS) far beyond any approved treatment and without any of the horrible side effects.
For the sake of those suffering from this devastating and heartbreaking disease, let’s all hope DCVAX gets approval and quickly.
If it doesn’t based on the use of historical controls due to compassionate crossover of the trial’s original control arm and a reordering of endpoints to address a newly discovered issue of pseudo progression, then it will be be one of the biggest travesties in the history of medicine. The suffering of us investors will pale in comparison to the millions of patients and families that will be destroyed.
Recent NWBO News
- 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
