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Maximum time between randomization and those deaths observed in FU was up to approximately 297 weeks.","eventGroups":[{"deathsNumAffected":59,"deathsNumAtRisk":123,"description":"Participants received carfilzomib 20 mg/m\\^2, IV infusion on Days 1, and 2 in Cycle 1, and then escalated to 56 mg/m\\^2 on Days 8, 9, 15 and 16 of Cycle 1 and then on Days 1, 2, 8, 9, 15 and 16 of each subsequent 28-day treatment cycle along with dexamethasone 20 mg, PO or IV on Days 1, 2, 8, 9, 15, 16, 22 and 23 of each 28-day treatment cycle until disease progression or unacceptable adverse event or participant's decision to discontinue the study treatment or any other reason, whichever comes first (maximum exposure: 349 weeks).","id":"EG000","otherNumAffected":113,"otherNumAtRisk":122,"seriousNumAffected":74,"seriousNumAtRisk":122,"title":"Carfilzomib + Dexamethasone (Kd)"},{"deathsNumAffected":83,"deathsNumAtRisk":179,"description":"Participants received isatuximab 10 mg/kg, IV infusion on Days 1, 8, 15 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TEAEs that developed, worsened, or became serious during the treatment period were assessed from first dose of study treatment administration (Day 1) up to 30 days post last dose of study treatment administration, up to 349 weeks for Kd arm and 356 weeks for IKd arm (maximum duration of treatment exposure)."}