This is very interesting and we’ll have a completely new, different aspect in treating CLL. For example, the BTK inhibitor pirtobrutinib is a BTK inhibitor which is binding non-covalently to BTK and therefore still acting in patients having the BTK resistance mutation.
And first data on patients having received prior other BTK inhibitors, shown very good response data and therefore the substance is currently developed in clinical trials and hopefully available in a few, very few years...
This is very interesting and we’ll have a completely new, different aspect in treating CLL. For example, the BTK inhibitor pirtobrutinib is a BTK inhibitor which is binding non-covalently to BTK and therefore still acting in patients having the BTK resistance mutation.
And first data on patients having received prior other BTK inhibitors, shown very good response data and therefore the substance is currently developed in clinical trials and hopefully available in a few, very few years. And then we will, similar as in CML, have also different options of treatment with BTK inhibitors, which act differently.
And this will be a completely new aspect for the treatment of CLL patients because then we could delay the time point where refractoriness is becoming a significant event for patients over survival and we can delay this time point for them.