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Do you know... In the phase III SUCCESSOR-2 trial, by approximately how much did MeziKd reduce the risk of disease progression or death vs Kd alone?
Patients with relapsed/refractory multiple myeloma (RRMM) who have been exposed or are refractory to lenalidomide and an anti-CD38 monoclonal antibody represent a growing population with limited validated treatment options. Mezigdomide, an oral cereblon E3 ligase modulator (CELMoD), is under investigation in combination with carfilzomib + dexamethasone (MeziKd) for the treatment of patients with RRMM whose disease has progressed after ≥1 prior line of therapy.
SUCCESSOR-2 (NCT05552976) is a randomized, phase III trial evaluating MeziKd vs Kd alone in this patient population. The primary endpoint is progression-free survival (PFS), with overall survival as a key secondary endpoint.
Here, we present a visual abstract summarizing key efficacy and safety findings from the phase III SUCCESSOR-2 trial.

This educational resource is independently supported by BMS. All content is developed by SES in collaboration with an expert steering committee. Funders are allowed no influence.
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Regarding bispecific antibodies for multiple myeloma, which of the following do you consider the biggest hurdle for patients and caregivers?