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For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG001","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"2: CFZ 15 mg/m² + LEN 15 mg"},{"description":"Treatment during Cycles 1 through 12 consisted of carfilzomib 15 mg/m² on Days 1, 2, 8, 9, 15, and 16; lenalidomide 20 mg on Days 1 to 21; and 40 mg dexamethasone on Days 1, 8, and 15, and 22. For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG002","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":4,"seriousNumAtRisk":8,"title":"3: CFZ 15 mg/m² + LEN 20 mg"},{"description":"Treatment during Cycles 1 through 12 consisted of carfilzomib 20 mg/m² on Days 1, 2, 8, 9, 15, and 16; lenalidomide 20 mg on Days 1 to 21; and 40 mg dexamethasone on Days 1, 8, and 15, and 22. For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG003","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"4: CFZ 20 mg/m² + LEN 20 mg"},{"description":"Treatment during Cycles 1 through 12 consisted of carfilzomib 20 mg/m² on Days 1, 2, 8, 9, 15, and 16; lenalidomide 25 mg on Days 1 to 21; and 40 mg dexamethasone on Days 1, 8, and 15 and 22. For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG004","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"5: CFZ 20 mg/m² + LEN 25 mg"},{"description":"Treatment consisted of carfilzomib 20 mg/m² on Days 1 and 2 of Cycle 1, followed by 27 mg/m² for the remainder of treatment (Days 8, 9, 15, and 16 of Cycle 1 and Days 1, 2, 8, 9, 15, and 16 for all subsequent cycles); lenalidomide 25 mg on Days 1 to 21; and 40 mg dexamethasone on Days 1, 8, and 15 and 22. For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG005","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":6,"seriousNumAtRisk":8,"title":"6: CFZ 20/27 mg/m² + LEN 25 mg"},{"description":"In the Expansion portion, treatment consisted of carfilzomib 20 mg/m² on Days 1 and 2 of Cycle 1, followed by 27 mg/m² for the remainder of treatment (Days 8, 9, 15, and 16 of Cycle 1 and Days 1, 2, 8, 9, 15, and 16 for all subsequent cycles); lenalidomide 25 mg on Days 1 to 21; and 40 mg dexamethasone on Days 1, 8, and 15 and 22. For Cycles 13 and higher, carfilzomib could be omitted on Days 8 and 9 at the investigator's discretion.","id":"EG006","otherNumAffected":42,"otherNumAtRisk":44,"seriousNumAffected":22,"seriousNumAtRisk":44,"title":"7: CFZ 20/27 mg/m² + LEN 25 mg"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":6},{"groupId":"EG001","numAffected":2,"numAtRisk":6},{"groupId":"EG002","numAffected":6,"numAtRisk":8},{"groupId":"EG003","numAffected":2,"numAtRisk":6},{"groupId":"EG004","numAffected":3,"numAtRisk":6},{"groupId":"EG005","numAffected":3,"numAtRisk":8},{"groupId":"EG006","numAffected":14,"numAtRisk":44}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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