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HyGro

09/14/22 8:55 PM

#513952 RE: Roman516 #513792

PFS was the primary endpoint of the DCVax-L trial. naive OS was the secondary endpoint. From the original protocol posted on clinicaltrials.gov:

Primary Outcome Measures:
1. The primary objective of this study is to compare progression free survival from time of randomization between patients treated with DCVax-L and control patients.
[ Time Frame: Time to tumor progression or death ]

Secondary Outcome Measures:
1. The secondary objective is to compare overall survival and time to disease progression between DCVax-L treated and control patients.
[ Time Frame: Until Death ]

Bottomline, PFS and OS are both "REAL" data results.