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Sunday, July 14, 2024 12:49:12 PM
I will assume this is simply ignorance and not baseless pumping,.
The patient level data in question is from the ECA.. NWBO does not posses it, so cannot provide. There is a reason why the FDA and others state this level of data is needed. And this submission does not have. And even the JAMA paper notes it, are they lying?
Moreover, Mr ignorant Basher, if NWBO ignored the FDA mandate to (for logical ethical reasons) have the placebo GBM patients NOT randomize to the treatment arm and thus die to be able to compare this data with the treatment arm then that would have made no difference with ECA comparing. You see my ignorant basher friend every person is different. To imply that the medical trial could have only been conducted by comparing a placebo group with a treatment group is BS not even considering the ethical problems this presents. A placebo group (with SOC treatment of course) is by definition a different set of people besides age and gender than a treatment arm simply because as I just said every person and patient is different. Therefore comparing DCVAXL-treated patients with ECA is the same as comparing it if they had compared it with a placebo group if not much better.
Crickets
Are you saying the video posted here was a fake?
SHOW ME THAT VIDEO NOW. Yes Im saying alomst everything you say is fake
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