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Maverick0408

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Maverick0408

Re: Doc logic post# 597858

Friday, 06/02/2023 6:34:19 PM

Friday, June 02, 2023 6:34:19 PM

Post# of 702118
Manual production is not the issue for the regulatory application and approval. FDA or MHRA will not reject an application because of manual vs automated production and you know that. Pretty much all CAR-T therapies are done manually and their addressable patient base (even for a single indication) is much larger than GBM.

I will tell you this - if we’re to wait for Flaskworks, then 2024 will be a lost year too. Hopefully, they will submit an application in 2025 or later.
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