Tuesday, April 21, 2015 10:20:19 PM
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.
ORR achieves faster approval.
Just musing while we await more data.
Respect Risk. Conduct Your Own Due Diligence. Manage your assets wisely. Diversify.
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