Now, talking about the non-covalent BTK inhibitors, we present a couple of studies with nemtabrutinib. Nemtabrutinib is another non-covalent BTK inhibitor developed slightly slower than pirtobrutinib, but in general very similar. So in the studies, once we presented efficacy in follicular lymphoma, that’s what we anticipated would happen. In follicular lymphoma, we used to have a much better result with PI3K inhibitors, which are eventually abandoned, and for the inhibition of BTK, we need a strong drug, a strong inhibition...
Now, talking about the non-covalent BTK inhibitors, we present a couple of studies with nemtabrutinib. Nemtabrutinib is another non-covalent BTK inhibitor developed slightly slower than pirtobrutinib, but in general very similar. So in the studies, once we presented efficacy in follicular lymphoma, that’s what we anticipated would happen. In follicular lymphoma, we used to have a much better result with PI3K inhibitors, which are eventually abandoned, and for the inhibition of BTK, we need a strong drug, a strong inhibition. And that’s why the first approval was with zanubrutinib and obinutuzumab. Now, both second-generation BTK inhibitors, specifically nemtabrutinib, was tested in this population with reasonable results. Again, the same thing as with Pirtobrutinib, relatively good efficacy and a great tolerance.
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