At this meeting we presented the updated results of this novel drug called BGB-16673 that is acting by a degradation of BTK. So it’s a BTK degrader, it’s targeting BTK and leading to the polyubiquitination and then proteasomal degradation within the cells of the protein. And we are now working on this drug in the setting of patients with relapsed/refractory CLL and there are preliminary data suggesting that the drug might work even in heavily pretreated patients including patients exposed to covalent BTK inhibitor, BCL2 inhibitor and non-covalent BCL2 inhibitor...
At this meeting we presented the updated results of this novel drug called BGB-16673 that is acting by a degradation of BTK. So it’s a BTK degrader, it’s targeting BTK and leading to the polyubiquitination and then proteasomal degradation within the cells of the protein. And we are now working on this drug in the setting of patients with relapsed/refractory CLL and there are preliminary data suggesting that the drug might work even in heavily pretreated patients including patients exposed to covalent BTK inhibitor, BCL2 inhibitor and non-covalent BCL2 inhibitor. So it’s a phase I/II study. We have initial data but they look very promising. So I hope that in the next future we can add this additional drug to our therapeutic armamentarium in CLL.
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