Yeah, I think I would say two. The first is understanding how to manage on-target tumor-associated inflammatory neurologic impacts for patients with glioblastoma. So that experiential, you know, knowledge, I certainly believe was really key and important to the overall clinical benefit that we were able to see. Because essentially, when it comes to cell therapy, CAR therapy to GBM, you know, we want that anticipated immune response to occur...
Yeah, I think I would say two. The first is understanding how to manage on-target tumor-associated inflammatory neurologic impacts for patients with glioblastoma. So that experiential, you know, knowledge, I certainly believe was really key and important to the overall clinical benefit that we were able to see. Because essentially, when it comes to cell therapy, CAR therapy to GBM, you know, we want that anticipated immune response to occur. We want the on-target efficacy and engagement to happen. And when it comes to the brain, that on-target tumor-associated inflammation can cause neurologic sequelae. So we have to learn how to manage through that neurologic impact in order to maintain ongoing therapeutic potential. So I would say that one is really key. And that comes back to, again, the methodology of how frequently to give the B7H3 CAR T cell therapy, how you want to allow for that on-target immune inflammatory impact while not giving too much time for the tumor cells to replicate and take over, right? So it’s finding that balance of the scheduled, you know, dosing parameters while also managing through the inflammatory impacts in patient care.
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