Wednesday, March 16, 2022 2:25:53 PM
1. It will indirectly shorten time to prove automated DCVax-l production equivalent to manual. Good for originating company and patients.
2. Once IP protections are expired (Aka: patents, exclusive use) it will make it easier/faster for generics/biosimilars to encroach on originating Company profits and reduce biological product prices. Good for biosimilar companies and patients.
3. It will create a biological state of the art arms race, wherein the original company will keep developing better, faster and more cost effective manufacturing to stay one step ahead of competition economics. Good for originating company and patients.
4. It will drive companies like NWBO to speed up Direct development once/if L is approved, in order to move toward new IP protections which biosimilars will not be able to compete against until about 2035. Good for originating company and patients.
Note: not everything here is rosy for patients, because big pharma tends to roll out new/better treatments after the prior treatment has lost IP protection. It is a given for most companies, and a flaw in the system.
2. Once IP protections are expired (Aka: patents, exclusive use) it will make it easier/faster for generics/biosimilars to encroach on originating Company profits and reduce biological product prices. Good for biosimilar companies and patients.
3. It will create a biological state of the art arms race, wherein the original company will keep developing better, faster and more cost effective manufacturing to stay one step ahead of competition economics. Good for originating company and patients.
4. It will drive companies like NWBO to speed up Direct development once/if L is approved, in order to move toward new IP protections which biosimilars will not be able to compete against until about 2035. Good for originating company and patients.
Note: not everything here is rosy for patients, because big pharma tends to roll out new/better treatments after the prior treatment has lost IP protection. It is a given for most companies, and a flaw in the system.
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
