I’ve been very excited to have commercial approval for pirtobrutinib in the United States that came earlier this year. Of course, a lot of us had been getting away with using it off-label when we needed it, because it was commercially available in mantle cell for some time previous to this approval. But it’s nice to not have to ask permission from the insurance companies to have the on-label approval...
I’ve been very excited to have commercial approval for pirtobrutinib in the United States that came earlier this year. Of course, a lot of us had been getting away with using it off-label when we needed it, because it was commercially available in mantle cell for some time previous to this approval. But it’s nice to not have to ask permission from the insurance companies to have the on-label approval.
It is sort of firmly rooted right now based on its label in the third line plus space, but that is a space where patients were lacking really safe and effective treatment options. Historically, we had been thinking about PI3 kinase inhibitors like duvelisib in this area, but pirtobrutinib certainly appears to be better tolerated, incredibly low discontinuation rates due to toxicity. And although it doesn’t give us the long progression-free survivals that we see with, say, first-line BTK inhibition, it is now a really good third-line option for our CLL patients that have needs beyond covalent BTK and BCL2 inhibition.