Thank you for your post, you make good arguments. If you read my previous posts, I do not disagree. There is as I said before just a fews BUT's. For all this to take place NWBO, UNDER PRESENT FDA REGULATIONS, needs to step and lift up its present platform! Now, again under present FDA regulation, NWBO will "only" receive permission to administer treatment for GBM.
Yes you are right when you say:
And in theory it shouldn't matter what part of the body the primary tumor started, so DCVAX could be used on all solid tumors
But that's a big IF. It would mean that the FDA does need to give this permission first. So for NWBO to cater a bigger market than "just" GBM the FDA mountain has to move or NWBO has to start acting and expand its product. Or both.
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