So the relapsed population now is changing a lot. Some years ago, even some months ago, I would say, maybe some years, we had a triple-class refractory as an admitted medical need. Now we have many different options for these patients. In fact, well, we have approved now several bispecifics, anti-BCMA, anti-GPRC5D. We also have the CAR-Ts. We have some other mechanisms of action. So probably now the medical needs have changed in this situation, And these are those patients that are, I would say, the four-class refractory that are also refractory to these T-cell engagers or the CAR-Ts...
So the relapsed population now is changing a lot. Some years ago, even some months ago, I would say, maybe some years, we had a triple-class refractory as an admitted medical need. Now we have many different options for these patients. In fact, well, we have approved now several bispecifics, anti-BCMA, anti-GPRC5D. We also have the CAR-Ts. We have some other mechanisms of action. So probably now the medical needs have changed in this situation, And these are those patients that are, I would say, the four-class refractory that are also refractory to these T-cell engagers or the CAR-Ts. And in fact, this is what we need now. What we are working on doing that is to know how we can sequence this data and we can use a bispecific followed by a CAR-T or the other way around. We can rescue what is the best bridging therapy we can do for these patients. But I think we have moved this patient, the unmet medical need, to one line later, which is those patients that have already received the T-cell redirecting therapies.
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