So bexobrutideg is a BTK inhibitor which has been looked at in multiple B-cell histologies. What I will be presenting the data on is the patients with relapsed refractory CLL. There is an update on the longer follow-up on these patients where we are seeing that at 18 months, estimated PFS is around 55% for these patients who have been heavily pretreated with multiple lines of therapy, including covalent BTK inhibitors, non-covalent BTK inhibitors, and BCL2 inhibitors...
So bexobrutideg is a BTK inhibitor which has been looked at in multiple B-cell histologies. What I will be presenting the data on is the patients with relapsed refractory CLL. There is an update on the longer follow-up on these patients where we are seeing that at 18 months, estimated PFS is around 55% for these patients who have been heavily pretreated with multiple lines of therapy, including covalent BTK inhibitors, non-covalent BTK inhibitors, and BCL2 inhibitors. So what we are looking at now is that bexobrutideg was able to salvage these patients and we’re seeing durable responses in a number of patients now. What also will be presented would be the use of the drug in earlier lines of therapy with patients who’ve had no previous line of therapy, as well as a cohort where the only line of therapy was a covalent BTK inhibitor, I’m suggesting that this approach can be used in earlier lines of therapy. And further trials are going to be looking at this question of use of this drug in earlier lines of therapy.
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