In this particular trial, we’re able to show that the combination of an oral CELMoD, mezigdomide, with carfilzomib, given weekly IV, and dexamethasone, was associated with a respectable median PFS of 18 months, in a relatively heavily pre-treated patient population with a median of two prior lines of therapy and with about 25% of our patients having received four or more therapies...
In this particular trial, we’re able to show that the combination of an oral CELMoD, mezigdomide, with carfilzomib, given weekly IV, and dexamethasone, was associated with a respectable median PFS of 18 months, in a relatively heavily pre-treated patient population with a median of two prior lines of therapy and with about 25% of our patients having received four or more therapies. Particularly, these patients reflect real-world patients because they had to be pre-treated and resistant to lenalidomide and pre-treated with anti-CD38. So I believe that we have a combination that could be applicable across different clinical settings with a predictable toxicity. We know that mezigdomide is associated with neutropenia. Neutropenia is short-lived. It can ameliorate with holding the drug or by administering G-CSF. We did not have unusual opportunistic infections and I believe that this combination could be given in different patient population and also in between anti-BCMA therapies because there is also evidence that mezigdomide may restore T-cell exhaustion.
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