I think there are three or four major combination therapies in MF. One of those is surely represented by ruxolitinib plus selinexor. I think we are having very good results both in terms of SVR and in terms of initial, very early sign of survival, they have to be confirmed because it’s a very early sign at the 24th week. But we are confident that probably patients with intermediate to high risk can really benefit from a combo...
I think there are three or four major combination therapies in MF. One of those is surely represented by ruxolitinib plus selinexor. I think we are having very good results both in terms of SVR and in terms of initial, very early sign of survival, they have to be confirmed because it’s a very early sign at the 24th week. But we are confident that probably patients with intermediate to high risk can really benefit from a combo. And it could be also an interesting proposal for those who will need to speed up their spleen response. Another drug that might be combined to drugs to increase the rate of SVR is surely pelabresib and we have long-term data showing that. Then there are some interesting exploratory combinations. One is in the phase 3 as well and it’s represented and devised as an add-on to ruxolitinib for those who are experiencing a suboptimal response or for those who are not responding to ruxolitinib and the add-on of navtemadlin can increase the apoptotic pathways in order to make the patient feel better and have major spleen responses. The fourth one I would like to mention is a phase one and it’s a combination between momelotinib and navtemadlin and patients who are cytopenic with anemia can benefit from that because the hematological toxicity seems to be very low.
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