The purpose of this study is to assess the efficacy and safety of cevostamab in combination with pomalidomide and dexamethasone (CevosPd) versus standard of care (SOC) in participants with multiple myeloma (MM) who have received one to three prior lines of therapy and have been exposed to an anti-CD38 monoclonal antibody (mAb) and lenalidomide.
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Minimal Residual Disease (MRD)-Negative Complete Response (CR) Rate
Timeframe: Up to 1 year after the last participant is randomized
Progression-Free Survival (PFS)
Timeframe: Up to 5 years after the last participant is randomized
Reference Study ID Number: CO46096 https://forpatients.roche.com/