Thursday, December 28, 2023 12:53:45 PM
Per the guidance, once the clock starts (Validation or "Acceptance") Assessment phase I will be completed within 80 days. During this period, eligibility for grant of orphan status is also determined. If there are issues requiring clarification (RFI), the clock turns off and RFI should be address within 60 days. NWBO can request an extension of an additional 60 days, but these are granted only for exceptions (not common).
Once RFI is addressed and sent to MHRA, clock turns back on and they have 70 days to provide a decision on approvability.
Max time: 80-Phase I+60-RFI+60-RFI Extension+70 = 270 days - > September 30th approval
Min time: Either no RFI (improbable) or RFI for simple things -> Approval a few weeks after CHM meeting scheduled for March 21 & March 22.
I think there is a possibility that we are approved by MHRA by the end of March, early April. The MHRA knows the treatment well, has been through the manufacturing facility several times, and the safety profile of the treatment has an excellent benefit/risk profile.
Once RFI is addressed and sent to MHRA, clock turns back on and they have 70 days to provide a decision on approvability.
Max time: 80-Phase I+60-RFI+60-RFI Extension+70 = 270 days - > September 30th approval
Min time: Either no RFI (improbable) or RFI for simple things -> Approval a few weeks after CHM meeting scheduled for March 21 & March 22.
I think there is a possibility that we are approved by MHRA by the end of March, early April. The MHRA knows the treatment well, has been through the manufacturing facility several times, and the safety profile of the treatment has an excellent benefit/risk profile.
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
- 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
