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Re: flipper44 post# 33739

Tuesday, 04/21/2015 10:20:19 PM

Tuesday, April 21, 2015 10:20:19 PM

Post# of 828171
Of course if you wanted to simply use PFS and OS as the primary and secondary endpoints for DCVax-L + CI combination trials, you could simply use the extracted tumors to make the lysate, but I think the thought is using the same patient profiles used previously for the CI trials which used ORR, but designing L in there as well as the pretreatment and concurrent combinational therapy.

ORR achieves faster approval.

Just musing while we await more data.

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