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Monday, 12/13/2021 2:10:25 PM

Monday, December 13, 2021 2:10:25 PM

Post# of 705733
Out of curiosity, in testing the FlaskWork device, do people here believe that they use patients who's tumor is sufficient to make two batches of the vaccine, one made in a clean room, the other by FlaskWork and comparing the two. I wonder if these patients are getting the vaccine under compassionate use, and paying for it, or if it's considered a trial, where the company is paying. In terms of what the patient receives, until the FlaskWork is deemed to be acceptable, I'd think they'd receive the conventionally made vaccine.

I believe the company is all in for FlaskWork's and planning for commercial production that's totally reliant on it. That said, I do believe they'll certify sufficient clean room capability to gain approvals even if FlaskWork is delayed. I still believe that CRL is the key to using a massive number of clean rooms, but in time they'll also have an arrangement for the FlaskWork device once it's approved.

Gary
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