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Hopeforthefuture3

12/14/25 3:10 PM

#802887 RE: Roman516 #802882

Roman, where do you get 'facts prove nwbo OS data surpassed the P3 data'?
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HyGro

12/14/25 9:06 PM

#802931 RE: Roman516 #802882

FDA & NWBO agreed that PFS was the primary endpoint - and DCVax-L didn't meet the primary endpoint. And right before the datalock, NWBO changed the protocol, the endpoints, the comparator - violating FDA guidance. Introduce significant bias into the trial that makes FDA very unhappy. And voila, FDA won't accept the data from the trial. That simple. NWBO has had almost three years to file with the FDA and has not.
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DocLee

12/15/25 2:27 AM

#802940 RE: Roman516 #802882

No wonder you don't flourish, NoGrow, with BS statements like this:

"NWBO clearly did not get the green light from FDA to file based on the P3 data" Not so . "The heavily manipulated trial violated multiple FDA guidelines regardless of how you spin it". Not So "That's why NWBO went to the UK. Not So

Tired old disproven lies and BS coming from a tired old liar and BS-er.