{"description":"Same event may appear as both non-SAE and SAE but are distinct events. An event may be categorized as serious in 1 participant and non-serious in another, or a participant may have experienced both SAE and non-SAE. Safety analysis set included all participants who received at least 1 full or partial dose of study medication.","eventGroups":[{"deathsNumAffected":2,"deathsNumAtRisk":2,"description":"Participants with relapsed/refractory advanced multiple myeloma (MM) received PF-06863135 at a dose of 0.1 microgram/kilogram (mcg/kg) as an intravenous (IV) infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG000","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"Part 1: PF-06863135 0.1 mcg/kg IV"},{"deathsNumAffected":2,"deathsNumAtRisk":3,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 0.3 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG001","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":1,"seriousNumAtRisk":3,"title":"Part 1: PF-06863135 0.3 mcg/kg IV"},{"deathsNumAffected":2,"deathsNumAtRisk":2,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 1 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG002","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"Part 1: PF-06863135 1 mcg/kg IV"},{"deathsNumAffected":3,"deathsNumAtRisk":3,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 3 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG003","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":3,"seriousNumAtRisk":3,"title":"Part 1: PF-06863135 3 mcg/kg IV"},{"deathsNumAffected":2,"deathsNumAtRisk":2,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 10 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG004","otherNumAffected":2,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"Part 1: PF-06863135 10 mcg/kg IV"},{"deathsNumAffected":4,"deathsNumAtRisk":5,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 30 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG005","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":2,"seriousNumAtRisk":5,"title":"Part 1: PF-06863135 30 mcg/kg IV"},{"deathsNumAffected":4,"deathsNumAtRisk":6,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 50 mcg/kg as an IV infusion for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG006","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":5,"seriousNumAtRisk":6,"title":"Part 1: PF-06863135 50 mcg/kg IV"},{"deathsNumAffected":5,"deathsNumAtRisk":6,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 80 mcg/kg as a subcutaneous (SC) injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG007","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"Part 1: PF-06863135 80 mcg/kg SC"},{"deathsNumAffected":1,"deathsNumAtRisk":4,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 130 mcg/kg as a SC injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG008","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":1,"seriousNumAtRisk":4,"title":"Part 1: PF-06863135 130 mcg/kg SC"},{"deathsNumAffected":3,"deathsNumAtRisk":4,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 215 mcg/kg as a SC injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG009","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":3,"seriousNumAtRisk":4,"title":"Part 1: PF-06863135 215 mcg/kg SC"},{"deathsNumAffected":3,"deathsNumAtRisk":4,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 360 mcg/kg as a SC injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG010","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":3,"seriousNumAtRisk":4,"title":"Part 1: PF-06863135 360 mcg/kg SC"},{"deathsNumAffected":3,"deathsNumAtRisk":6,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 600 mcg/kg as a SC injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG011","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"Part 1: PF-06863135 600 mcg/kg SC"},{"deathsNumAffected":2,"deathsNumAtRisk":6,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a dose of 1000 mcg/kg as a SC injection on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG012","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":5,"seriousNumAtRisk":6,"title":"Part 1: PF-06863135 1000 mcg/kg SC"},{"deathsNumAffected":3,"deathsNumAtRisk":7,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 600 mcg/kg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 1000 mcg/kg as a SC injection every week (Q1W) on Day 1, 8, 15 and 22 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG013","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":6,"seriousNumAtRisk":7,"title":"Part 1.1: PF-06863135 Priming Cohort Q1W SC"},{"deathsNumAffected":4,"deathsNumAtRisk":13,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 600 mcg/kg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 1000 mcg/kg as a SC injection every 2 weeks (Q2W) on Day 1 and 15 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG014","otherNumAffected":13,"otherNumAtRisk":13,"seriousNumAffected":9,"seriousNumAtRisk":13,"title":"Part 1.1: PF-06863135 Priming Cohort Q2W SC"},{"deathsNumAffected":2,"deathsNumAtRisk":4,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 32 mcg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 44 mcg as a SC injection Q1W on Day 1, 8, 15 and 22 along with lenalidomide at dose of 15 mg, orally, daily on Days 1-21 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG015","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":2,"seriousNumAtRisk":4,"title":"Part 1C: PF-06863135 + Lenalidomide SC"},{"deathsNumAffected":4,"deathsNumAtRisk":9,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 32 mcg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 44 mcg as a SC injection Q1W on Day 1, 8, 15 and 22 along with pomalidomide at dose of 4 mg, orally, daily on Days 1-21 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG016","otherNumAffected":9,"otherNumAtRisk":9,"seriousNumAffected":8,"seriousNumAtRisk":9,"title":"Part 1D: PF-06863135 + Pomalidomide SC"},{"deathsNumAffected":10,"deathsNumAtRisk":15,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 44 mcg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 76 mcg as a SC injection Q1W on Day 1, 8, 15 and 22 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG017","otherNumAffected":13,"otherNumAtRisk":15,"seriousNumAffected":12,"seriousNumAtRisk":15,"title":"Part 2A: PF-06863135 SC"},{"deathsNumAffected":19,"deathsNumAtRisk":23,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 as an IV infusion (any dose) for 2 hours on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG018","otherNumAffected":23,"otherNumAtRisk":23,"seriousNumAffected":11,"seriousNumAtRisk":23,"title":"Part 1: PF-06863135 Total IV"},{"deathsNumAffected":17,"deathsNumAtRisk":30,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 as a SC injection (any dose) on Day 1, 8 and 15 of each 21-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG019","otherNumAffected":30,"otherNumAtRisk":30,"seriousNumAffected":20,"seriousNumAtRisk":30,"title":"Part 1: PF-06863135 Total SC"},{"deathsNumAffected":7,"deathsNumAtRisk":20,"description":"Participants with relapsed/refractory advanced MM received PF-06863135 at a priming dose of 600 mcg/kg as a SC injection, on Day 1 of Cycle 0. Participants received maintenance dose of 1000 mcg/kg as a SC injection Q1W on Day 1, 8 ,15 and 22 of each 28-day cycle or Q2W on Day 1 and 15 of each 28-day cycle. Participants received treatment until disease progression, unacceptable toxicity, withdrawal of consent, death, or study termination, whichever occurred first.","id":"EG020","otherNumAffected":20,"otherNumAtRisk":20,"seriousNumAffected":15,"seriousNumAtRisk":20,"title":"Part 1.1: PF-06863135 Total SC"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v26.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":2},{"groupId":"EG001","numAffected":2,"numAtRisk":3},{"groupId":"EG002","numAffected":1,"numAtRisk":2},{"groupId":"EG003","numAffected":1,"numAtRisk":3},{"groupId":"EG004","numAffected":2,"numAtRisk":2},{"groupId":"EG005","numAffected":4,"numAtRisk":5},{"groupId":"EG006","numAffected":3,"numAtRisk":6},{"groupId":"EG007","numAffected":4,"numAtRisk":6},{"groupId":"EG008","numAffected":3,"numAtRisk":4},{"groupId":"EG009","numAffected":3,"numAtRisk":4},{"groupId":"EG010","numAffected":4,"numAtRisk":4},{"groupId":"EG011","numAffected":3,"numAtRisk":6},{"groupId":"EG012","numAffected":5,"numAtRisk":6},{"groupId":"EG013","numAffected":6,"numAtRisk":7},{"groupId":"EG014","numAffected":9,"numAtRisk":13},{"groupId":"EG015","numAffected":1,"numAtRisk":4},{"groupId":"EG016","numAffected":3,"numAtRisk":9},{"groupId":"EG017","numAffected":6,"numAtRisk":15},{"groupId":"EG018","numAffected":14,"numAtRisk":23},{"groupId":"EG019","numAffected":22,"numAtRisk":30},{"groupId":"EG020","numAffected":15,"numAtRisk":20}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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and lymphatic system disorders","sourceVocabulary":"MedDRA v26.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":2},{"groupId":"EG001","numAffected":1,"numAtRisk":3},{"groupId":"EG002","numAffected":1,"numAtRisk":2},{"groupId":"EG003","numAffected":1,"numAtRisk":3},{"groupId":"EG004","numAffected":1,"numAtRisk":2},{"groupId":"EG005","numAffected":2,"numAtRisk":5},{"groupId":"EG006","numAffected":3,"numAtRisk":6},{"groupId":"EG007","numAffected":4,"numAtRisk":6},{"groupId":"EG008","numAffected":3,"numAtRisk":4},{"groupId":"EG009","numAffected":4,"numAtRisk":4},{"groupId":"EG010","numAffected":4,"numAtRisk":4},{"groupId":"EG011","numAffected":5,"numAtRisk":6},{"groupId":"EG012","numAffected":6,"numAtRisk":6},{"groupId":"EG013","numAffected":3,"numAtRisk":7},{"groupId":"EG014","numAffected":4,"numAtRisk":13},{"groupId":"EG015","numAffected":3,"numAtRisk":4},{"groupId":"EG016","numAffected":3,"numAtRisk":9},{"groupId":"EG017","numAffected":3,"numAtRisk":15},{"groupId":"EG018","numAffected":9,"numAtRisk":23},{"groupId":"EG019","numAffected":26,"numAtRisk":30},{"groupId":"EG020","numAffected":7,"numAtRisk":20}],"term":"Lymphopenia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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and lymphatic system disorders","sourceVocabulary":"MedDRA 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disorders","sourceVocabulary":"MedDRA v26.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":2},{"groupId":"EG001","numAffected":0,"numAtRisk":3},{"groupId":"EG002","numAffected":0,"numAtRisk":2},{"groupId":"EG003","numAffected":0,"numAtRisk":3},{"groupId":"EG004","numAffected":0,"numAtRisk":2},{"groupId":"EG005","numAffected":0,"numAtRisk":5},{"groupId":"EG006","numAffected":0,"numAtRisk":6},{"groupId":"EG007","numAffected":0,"numAtRisk":6},{"groupId":"EG008","numAffected":0,"numAtRisk":4},{"groupId":"EG009","numAffected":1,"numAtRisk":4},{"groupId":"EG010","numAffected":0,"numAtRisk":4},{"groupId":"EG011","numAffected":1,"numAtRisk":6},{"groupId":"EG012","numAffected":1,"numAtRisk":6},{"groupId":"EG013","numAffected":1,"numAtRisk":7},{"groupId":"EG014","numAffected":1,"numAtRisk":13},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":1,"numAtRisk":9},{"groupId":"EG017","numAffected":2,"numAtRisk":15},{"groupId":"EG018","numAffected":0,"numAtRisk":23},{"groupId":"EG019","numAffected":3,"numAtRisk":30},{"groupId":"EG020","numAffected":2,"numAtRisk":20}],"term":"Sinus 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