{"description":"Other Adverse Events summarizes the non-serious occurrences of adverse events that exceed the indicated frequency threshold.\n\nSummary of Adverse Events includes only those subjects who received at least one dose of investigational product.","eventGroups":[{"description":"Participants with solid tumors (ST) received carfilzomib (CFZ) 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Days 1, 2, 8, 9, 15, and 16 of a 28-day cycle. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG000","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":1,"seriousNumAtRisk":3,"title":"P1B ST: CFZ 20 mg/m² Bolus"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Cycle 1 Days 1 and 2 only, then 27 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG001","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":1,"seriousNumAtRisk":4,"title":"P1B ST: CFZ 20/27 mg/m² Bolus"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Cycle 1 Days 1 and 2 only, then 36 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG002","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":4,"seriousNumAtRisk":7,"title":"P1B ST: CFZ 20/36 mg/m² Bolus"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by bolus intravenous infusion over 2-10 minutes on Cycle 1 Days 1 and 2 only, then 36 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG003","otherNumAffected":65,"otherNumAtRisk":65,"seriousNumAffected":27,"seriousNumAtRisk":65,"title":"P2 ST: CFZ 20/36 mg/m² Bolus"},{"description":"Participants with solid tumors received carfilzomib 36 mg/m² administered by intravenous infusion over 30 minutes on Days 1, 2, 8, 9, 15, and 16 of a 28-day cycle for at least 2 cycles. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG004","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"P1B ST: CFZ 36 mg/m²"},{"description":"Participants with solid tumors received carfilzomib 45 mg/m² administered by intravenous infusion over 30 minutes on Days 1, 2, 8, 9, 15, and 16 of a 28-day cycle for at least 2 cycles. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG005","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":4,"seriousNumAtRisk":7,"title":"P1B ST: CFZ 45 mg/m²"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 45 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG006","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":5,"seriousNumAtRisk":6,"title":"P1B ST: CFZ 20/45 mg/m²"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 56 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG007","otherNumAffected":10,"otherNumAtRisk":10,"seriousNumAffected":5,"seriousNumAtRisk":10,"title":"P1B ST: CFZ 20/56 mg/m²"},{"description":"Participants with solid tumors received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 70 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG008","otherNumAffected":11,"otherNumAtRisk":11,"seriousNumAffected":6,"seriousNumAtRisk":11,"title":"P1B ST: CFZ 20/70 mg/m²"},{"description":"Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 36 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG009","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":2,"seriousNumAtRisk":4,"title":"P1B MM: CFZ 20/36 mg/m²"},{"description":"Participants with multiple myeloma (MM) received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 45 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG010","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":0,"seriousNumAtRisk":3,"title":"P1B MM: CFZ 20/45 mg/m²"},{"description":"Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 56 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG011","otherNumAffected":24,"otherNumAtRisk":24,"seriousNumAffected":11,"seriousNumAtRisk":24,"title":"P1B MM: CFZ 20/56 mg/m²"},{"description":"Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 70 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG012","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":2,"seriousNumAtRisk":2,"title":"P1B MM: CFZ 20/70 mg/m²"},{"description":"Participants with lymphoma (LYM) received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 56 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG013","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":1,"seriousNumAtRisk":3,"title":"P1B LYM: CFZ 20/56 mg/m²"},{"description":"Participants with lymphoma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 70 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG014","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":5,"seriousNumAtRisk":7,"title":"P1B LYM: CFZ 20/70 mg/m²"},{"description":"Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 45 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment plus dexamethasone 40 mg weekly. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG015","otherNumAffected":14,"otherNumAtRisk":14,"seriousNumAffected":5,"seriousNumAtRisk":14,"title":"P1B MM: CFZ 20/45 mg/m² + Dex"},{"description":"Participants with multiple myeloma received carfilzomib 20 mg/m² administered by intravenous infusion over 30 minutes on Cycle 1 Days 1 and 2 only, then 56 mg/m² on Days 8, 9, 15 and 16 and thereafter for the remainder of treatment plus dexamethasone 40 mg weekly. All participants with stable disease or better after 2 cycles could continue treatment until progressive disease or unacceptable toxicity.","id":"EG016","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":3,"seriousNumAtRisk":8,"title":"P1B MM: CFZ 20/56 mg/m² + Dex"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":0,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":0,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":1,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Febrile neutropenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":0,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":0,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":1,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Haemolytic anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":2,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":0,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":0,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Iron deficiency anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":1,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":1,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":1,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":0,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":1,"numAtRisk":8}],"term":"Leukocytosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":1,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":1,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":0,"numAtRisk":7},{"groupId":"EG015","numAffected":1,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Leukopenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":2,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":0,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":1,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":0,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":0,"numAtRisk":3},{"groupId":"EG014","numAffected":0,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Lymphadenopathy"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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disorders","sourceVocabulary":"MedDRA 8.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":3},{"groupId":"EG001","numAffected":0,"numAtRisk":4},{"groupId":"EG002","numAffected":0,"numAtRisk":7},{"groupId":"EG003","numAffected":0,"numAtRisk":65},{"groupId":"EG004","numAffected":0,"numAtRisk":6},{"groupId":"EG005","numAffected":0,"numAtRisk":7},{"groupId":"EG006","numAffected":0,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":10},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":3},{"groupId":"EG011","numAffected":4,"numAtRisk":24},{"groupId":"EG012","numAffected":0,"numAtRisk":2},{"groupId":"EG013","numAffected":1,"numAtRisk":3},{"groupId":"EG014","numAffected":1,"numAtRisk":7},{"groupId":"EG015","numAffected":0,"numAtRisk":14},{"groupId":"EG016","numAffected":0,"numAtRisk":8}],"term":"Neutropenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and 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