Well, the patients who’ve failed venetoclax, it’s an important subset of patients because the reality is nowadays most patients start with azacitidine and venetoclax, patients who are ineligible for intensive chemotherapy, because you don’t have to wait for mutations. And patients with IDH1 mutations respond very well to azacitidine-venetoclax, but it’s not curative. So this subset analysis shows that when you use olutasidenib after a patient has already received venetoclax and lost the response or didn’t respond, you get the same benefit as in patients that have never been treated with venetoclax, meaning it doesn’t reduce the possibility of responding to olutasidenib...
Well, the patients who’ve failed venetoclax, it’s an important subset of patients because the reality is nowadays most patients start with azacitidine and venetoclax, patients who are ineligible for intensive chemotherapy, because you don’t have to wait for mutations. And patients with IDH1 mutations respond very well to azacitidine-venetoclax, but it’s not curative. So this subset analysis shows that when you use olutasidenib after a patient has already received venetoclax and lost the response or didn’t respond, you get the same benefit as in patients that have never been treated with venetoclax, meaning it doesn’t reduce the possibility of responding to olutasidenib. We still see more than a third of patients responding, most of these responses are actually CRs, not just CRHs. They’re durable responses, very durable, more than two years duration of response. It’s a small subset of patients, but I think it’s a very important practical piece of information because that’s the reality of what we do. So it just gives us confidence that olutasidenib can work in that setting.