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Re: brazen22 post# 625198

Sunday, 08/27/2023 11:33:19 AM

Sunday, August 27, 2023 11:33:19 AM

Post# of 703872
brazen22,

I hear you—we are all eagerly anticipating press on regulatory advisory.

FDA is of course the focus, but I think that the U.K. will prove vastly significant too! King’s College and the Specials Program and MHRA developments are all very significant!

Additionally, I recommend that you review the forthcoming NICE appraisal of the DCVax-L cell-based technology. Stay tuned!


https://www.nice.org.uk/guidance/indevelopment/gid-ta10143




https://www.fda.gov/about-fda/oncology-center-excellence/project-orbis





https://www.kcl.ac.uk/people/keyoumars-ashkan

The MIA was approved recently and is evidence of a regulatory filing plan that has begun to unfold. Further RA applications have been under construction for a significant period of time and include a voluminous catalog of clinical data and analyses. The announcements of regulatory filings are forthcoming.

The recent MIA approval is an important step in the regulatory process, and this commercial manufacturing license will allow DCVax-L to be exported globally from Sawston. The MIA is a prerequisite of the MAA application.

“Companies applying for a marketing authorisation (also known as a product licence) need to have a manufacturer licence first. The manufacturer licence will be granted first providing the product is in the process of being approved.” —MHRA

https://www.gov.uk/guidance/apply-for-manufacturer-or-wholesaler-of-medicines-licences

https://finance.yahoo.com/news/northwest-biotherapeutics-advent-bioservices-announce-234600744.html

https://finance.yahoo.com/news/northwest-biotherapeutics-announces-approval-pediatric-133900403.html

https://investorshub.advfn.com/boards/read_msg.aspx?message_id=172639755%5B/color%5D
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