For CLL, of course, at this point we don’t have a lot of data, but we have some very compelling studies and evidence that CLL is a perfect target for copies and treatment. From the current evidence we have, it seems that the most active way to apply CARs in CLL, is not to use it in very late lines, and to combine it with ibrutinib, and that seems to lower toxicity and also increase the response rates in terms of MRD...
For CLL, of course, at this point we don’t have a lot of data, but we have some very compelling studies and evidence that CLL is a perfect target for copies and treatment. From the current evidence we have, it seems that the most active way to apply CARs in CLL, is not to use it in very late lines, and to combine it with ibrutinib, and that seems to lower toxicity and also increase the response rates in terms of MRD. So, I think it will probably be used the latest when a patient did not respond to at least two different treatments with an inhibitor. So, if a patient is even resistant, for instance, through a BTK.