The bispecific antibody epcoritamab is currently being developed in a Phase I/II trial in monotherapy but also in combination with venetoclax for example, as well as in Richter transformation. What we do see with this bispecific is that the cytokine release syndrome is occurring obviously more frequently than in other lymphoma entities. It seems that there is also a tendency towards more infections, particularly more severe infections, particularly when we use dexamethasone, for example, for prophylaxis of cytokine release syndrome...
The bispecific antibody epcoritamab is currently being developed in a Phase I/II trial in monotherapy but also in combination with venetoclax for example, as well as in Richter transformation. What we do see with this bispecific is that the cytokine release syndrome is occurring obviously more frequently than in other lymphoma entities. It seems that there is also a tendency towards more infections, particularly more severe infections, particularly when we use dexamethasone, for example, for prophylaxis of cytokine release syndrome. However, what is interesting, of course, is that even in heavily pre-treated patients, undetectable MRD rates can be achieved quite fast within three or four months of treatment. And therefore, I think we have to learn how we deal with the cytokine release syndrome, in particular in CLL and how we use this drug as the best treatment option if we should use it as continuous treatment or combining for a rather short course.