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Re: polska post# 733751

Wednesday, 11/27/2024 7:39:01 PM

Wednesday, November 27, 2024 7:39:01 PM

Post# of 821103
PFS is relevant because NWBO and FDA agreed that it was the PRIMARY ENDPOINT for the P3 trial. DCVax-L failed the primary endpoint and NWBO tossed it out and redid the whole trial protocol after the trial was virtually completed.
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