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Re: mike00h post# 627007

Thursday, 08/31/2023 11:03:50 AM

Thursday, August 31, 2023 11:03:50 AM

Post# of 698805
The FDA will have no problem approving DCVAXL on present RWE and SPA as currently presented by NWBO. The FDA could however decline a request for approval if NWBO does not have its production in order as it declined Outlook Therapeutics BLA.
https://finance.yahoo.com/news/outlook-therapeutics-provides-regulatory-fda-100000177.html

the Agency concluded it could not approve the BLA during this review cycle due to several CMC issues, open observations from pre-approval manufacturing inspections, and a lack of substantial evidence



I do not believe that the delay in submitting a BLA to the FDA has anything to do with consultants being slow, politics or data not being in order, it has everything todo with manufacturing capacity at Sawston or even CRL. Lets hope that NWBO's manufacturing capacity is in order after MHRA approval or otherwise we are in for another long wait after MHRA approval until the capacity or quantity is at the level it meets FDA criteria.
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