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Re: Doc logic post# 770535

Thursday, 06/05/2025 4:33:39 PM

Thursday, June 05, 2025 4:33:39 PM

Post# of 823836
Bullshit. Medicenna has a database of patient level data for their GBM trial. The FDA told them they needed it when THEY ACTUALLY MET WITH THEM in the P3 design phase, not after p3 failure.

It’s on the company to provide it as evidenced by the company’s inability to submit a BLA because the control is not only bullshit, but incomplete bullshit.
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