In the study update in 2021, at a median follow-up of 35.5 months, Isa-Pd was found to significantly improve time-to-next treatment and PFS2 and there was a strong trend in OS benefit in the Isa-Pd arm (24.6 versus 17.7 months, HR = 0.76). 48 In 2020, the EMA and FDA approved the combination of isatuximab-Pd for MM patients who have received at least two previous treatments, including lenalidomide and a PI.
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Pomalidomide- and dexamethasone-based regimens in the treatment of refractory/relapsed multiple myeloma.
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