So we have the approval now for cilta-cel in patients that had received at least one line of therapy, including an IMID and PI, and an anti-CD38 antibody, and being lenalidomide-refractory. So this is the patient where we have now the approval to go ahead with CAR T-cell therapy. And we have actually seen that also in patients that are much more heavily pretreated, CAR T-cell therapy in a fraction of patients, it’s about 33% of patients, can induce long-term disease-free survival...
So we have the approval now for cilta-cel in patients that had received at least one line of therapy, including an IMID and PI, and an anti-CD38 antibody, and being lenalidomide-refractory. So this is the patient where we have now the approval to go ahead with CAR T-cell therapy. And we have actually seen that also in patients that are much more heavily pretreated, CAR T-cell therapy in a fraction of patients, it’s about 33% of patients, can induce long-term disease-free survival. So the hope is, if we move it now to the second line, that we have an even larger percentage of patients that we see to benefit long-term from this treatment. And there is a hope that we can, even in relapsed patients, get some patients to achieve long-term remission and cure for multiple myeloma.
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