Det vi snakket om tidligere i dag;
They (Agenus) are running also PD1 and CTLA4 studies in melanoma, so which should allow us to sort of compare the data from different trails, and then satisfy the requirements of the FDA, to demonstrate contribution of different components.
And this also explains the individual components in the combination study, because obviously, eventually we are aiming at pretty sophisticated combinations, which will include our virus, anti PD1 and this new generation CTLA4. So we have to establish dosing, demonstrate contribution of individual components and then proceed to the pivotal study.
But the fact that we are doing the trail that i presented and that Agenus are running their own dose escalation studies and combination studies in melanoma. Will allow us to present the full package to the FDA