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All participants included in the Safety Analysis Set were included in this analysis.","eventGroups":[{"deathsNumAffected":4,"deathsNumAtRisk":15,"description":"Participants were administered IV melflufen at a dose of 30 mg on Day 1 of each 28-day cycle in combination with SQ bortezomib at a dose of 1.3mg/m\\^2 on Days 1, 4, 8, and 11 and dexamethasone PO at a dose of 20 mg (12 mg if the participants is ≥ 75 years of age) on Days 1, 4, 8, and 11 and 40 mg (20 mg if the participants is ≥ 75 years of age) on Day 15 and 22 of each 28-day cycle.","id":"EG000","otherNumAffected":15,"otherNumAtRisk":15,"seriousNumAffected":9,"seriousNumAtRisk":15,"title":"A (Melflufen+Bortezomib+Dex) 30 mg"},{"deathsNumAffected":2,"deathsNumAtRisk":8,"description":"Participants were administered IV melflufen at a dose of 40 mg on Day 1 of each 28-day cycle in combination with SQ bortezomib at a dose of 1.3mg/m\\^2 on Days 1, 4, 8, and 11 and dexamethasone PO at a dose of 20 mg (12 mg if the participants is ≥ 75 years of age) on Days 1, 4, 8, and 11 and 40 mg (20 mg if the participants is ≥ 75 years of age) on Day 15 and 22 of each 28-day cycle.","id":"EG001","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":5,"seriousNumAtRisk":8,"title":"A (Melflufen+Bortezomib+Dex) 40 mg"},{"deathsNumAffected":3,"deathsNumAtRisk":6,"description":"Participants were administered IV melflufen at a dose of 30 mg on Day 1 of each 28-day cycle in combination with daratumumab at a dose of 16 mg/kg weekly for 8 doses, every other week for 8 doses and then once every 4 weeks. Participants were also administered dexamethasone PO at a dose of 40 mg weekly (20 mg weekly if the participants is ≥ 75 years of age).","id":"EG002","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"B (Melflufen+Daratumumab+Dex) 30 mg"},{"deathsNumAffected":16,"deathsNumAtRisk":27,"description":"Participants were administered IV melflufen at a dose of 40 mg on Day 1 of each 28-day cycle in combination with daratumumab at a dose of 16 mg/kg weekly for 8 doses, every other week for 8 doses and then once every 4 weeks. Participants were also administered dexamethasone PO at a dose of 40 mg weekly (20 mg weekly if the participants is ≥ 75 years of age).","id":"EG003","otherNumAffected":27,"otherNumAtRisk":27,"seriousNumAffected":11,"seriousNumAtRisk":27,"title":"B (Melflufen+Daratumumab+Dex) 40 mg"}],"frequencyThreshold":"0","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA (24.0)","stats":[{"groupId":"EG000","numAffected":5,"numAtRisk":15},{"groupId":"EG001","numAffected":2,"numAtRisk":8},{"groupId":"EG002","numAffected":2,"numAtRisk":6},{"groupId":"EG003","numAffected":11,"numAtRisk":27}],"term":"Fatigue"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA 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