So in that trial, these are patients that are in the intermediate stage. And this is first line. So they’re systemically naive. We’re combining epoetin alfa was not mentioned but another drug was, and cabozantinib with TACE in those patients in hopes of extending overall survival and also progression-free survival. We did note a 28% complete response in that trial, which is very encouraging...
So in that trial, these are patients that are in the intermediate stage. And this is first line. So they’re systemically naive. We’re combining epoetin alfa was not mentioned but another drug was, and cabozantinib with TACE in those patients in hopes of extending overall survival and also progression-free survival. We did note a 28% complete response in that trial, which is very encouraging. There were not a lot of adverse events, which was pretty well tolerated, and so the combination of all three seemed to be positive. I think the main thing with this is that what we’re looking for, and this is something we noted, and it’s not mentioned in the abstract with the TTP or PFS or other study, but we have data on the TCR clones. So we’re looking at peripherally in the blood and we note that patients who have a response have an expansion of their CD8 clones and both new clones and expansion of existing clones. And I think, so there is immunomodulation by the combination therapy. And I think that’s kind of really the synergy and what’s at heart is that we need to find the right combinations to really induce that immune activation.
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