{"description":"The same event may appear as both AE and SAE. An event may be categorized as serious in 1 participant and non-serious in another participant, or 1 participant may have experienced both a serious and non-serious event during the study. For AE and SAE safety analysis set was analyzed. Safety analysis set includes all participants who received at least 1 dose of study drug. For All-Cause Mortality full analysis set was analyzed. Full analysis set includes all randomized participants in the study.","eventGroups":[{"deathsNumAffected":18,"deathsNumAtRisk":29,"description":"During phase 1b participants with Non-Small Cell Lung Cancer (NSCLC) received utomilumab 500 mg intravenously (IV) every 4 weeks (Q4W) with 10 milligrams per kilogram (mg/kg) of avelumab administered IV every 2 weeks (Q2W) for 2 cycles, where each cycle was of 4 weeks.","id":"EG000","otherNumAffected":29,"otherNumAtRisk":29,"seriousNumAffected":11,"seriousNumAtRisk":29,"title":"Combination A Phase 1b NSCLC: Utomilumab 500 mg + Avelumab"},{"deathsNumAffected":19,"deathsNumAtRisk":28,"description":"During phase 1b participants with NSCLC received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG001","otherNumAffected":27,"otherNumAtRisk":27,"seriousNumAffected":12,"seriousNumAtRisk":27,"title":"Combination A Phase 1b NSCLC: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":20,"deathsNumAtRisk":29,"description":"During phase 1b participants with NSCLC received utomilumab 20 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG002","otherNumAffected":28,"otherNumAtRisk":29,"seriousNumAffected":13,"seriousNumAtRisk":29,"title":"Combination A Phase 1b NSCLC: Utomilumab 20 mg + Avelumab"},{"deathsNumAffected":19,"deathsNumAtRisk":28,"description":"During Phase 2 participants with melanoma received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG003","otherNumAffected":28,"otherNumAtRisk":28,"seriousNumAffected":9,"seriousNumAtRisk":28,"title":"Combination A Phase 2 Melanoma: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":25,"deathsNumAtRisk":35,"description":"During Phase 2 participants with Squamous Cell Carcinoma of the Head and Neck (SCCHN) received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG004","otherNumAffected":33,"otherNumAtRisk":35,"seriousNumAffected":16,"seriousNumAtRisk":35,"title":"Combination A Phase 2 SCCHN: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":12,"deathsNumAtRisk":21,"description":"During Phase 2 participants with Triple Negative Breast Cancer (TNBC) received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG005","otherNumAffected":20,"otherNumAtRisk":21,"seriousNumAffected":4,"seriousNumAtRisk":21,"title":"Combination A Phase 2 TNBC: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":6,"deathsNumAtRisk":10,"description":"During Phase 2 participants with Squamous cell lung cancer (SCLC) received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG006","otherNumAffected":10,"otherNumAtRisk":10,"seriousNumAffected":4,"seriousNumAtRisk":10,"title":"Combination A Phase 2 SCLC: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":14,"deathsNumAtRisk":21,"description":"During Phase 2 participants with NSCLC received utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG007","otherNumAffected":21,"otherNumAtRisk":21,"seriousNumAffected":8,"seriousNumAtRisk":21,"title":"Combination A Phase 2 First Line (1L) NSCLC: Utomilumab 100 mg + Avelumab"},{"deathsNumAffected":7,"deathsNumAtRisk":11,"description":"During Phase 2 participants with NSCLC received utomilumab 100 mg IV Q4W for cycle 1 then utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W starting at cycle 2.","id":"EG008","otherNumAffected":11,"otherNumAtRisk":11,"seriousNumAffected":4,"seriousNumAtRisk":11,"title":"Combination A Phase 2 1L NSCLC: Utomilumab Then Utomilumab + Avelumab"},{"deathsNumAffected":6,"deathsNumAtRisk":11,"description":"During Phase 2 participants with NSCLC received avelumab 10 mg/kg administered IV Q2W for cycles 1 then utomilumab 100 mg IV Q4W with 10 mg/kg of avelumab administered IV Q2W starting at cycle 2.","id":"EG009","otherNumAffected":10,"otherNumAtRisk":11,"seriousNumAffected":1,"seriousNumAtRisk":11,"title":"Combination A Phase 2 1L NSCLC: Avelumab Then Utomilumab + Avelumab"},{"deathsNumAffected":7,"deathsNumAtRisk":12,"description":"During Phase 1b participants received PF-04518600 0.3 mg/kg IV Q2W with 10 mg/kg of avelumab administered IV Q2W. Phase 2 in the melanoma cohort was not planned.","id":"EG010","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":3,"seriousNumAtRisk":12,"title":"Combination B Phase 1b: PF-04518600 0.3 mg/kg + Avelumab"},{"deathsNumAffected":6,"deathsNumAtRisk":12,"description":"During Phase 1b participants received PF-04518600 1.0 mg/kg IV Q2W with 10 mg/kg of avelumab administered IV Q2W. Phase 2 in the melanoma cohort was not planned.","id":"EG011","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":4,"seriousNumAtRisk":12,"title":"Combination B Phase 1b: PF-04518600 1.0 mg/kg + Avelumab"},{"deathsNumAffected":6,"deathsNumAtRisk":8,"description":"During Phase 1b participants received PF-04518600 3.0 mg/kg IV Q2W with 10 mg/kg of avelumab administered IV Q2W. Phase 2 in the melanoma cohort was not planned.","id":"EG012","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":1,"seriousNumAtRisk":8,"title":"Combination B Phase 1b: PF-04518600 3.0 mg/kg + Avelumab"},{"deathsNumAffected":8,"deathsNumAtRisk":14,"description":"During Phase 2 participants with NSCLC received PF-04518600 0.3 mg/kg IV Q2W with 10 mg/kg of avelumab administered IV Q2W.","id":"EG013","otherNumAffected":14,"otherNumAtRisk":14,"seriousNumAffected":3,"seriousNumAtRisk":14,"title":"Combination B Phase 2 NSCLC: PF-04518600 0.3 mg/kg + Avelumab"},{"deathsNumAffected":21,"deathsNumAtRisk":25,"description":"During Phase 2 participants with SCCHN received PF-04518600 0.3 mg/kg IV Q2W with 10 mg/kg of avelumab administered IV Q2W.","id":"EG014","otherNumAffected":25,"otherNumAtRisk":25,"seriousNumAffected":10,"seriousNumAtRisk":25,"title":"Combination B Phase 2 SCCHN: PF-04518600 0.3 mg/kg + Avelumab"},{"deathsNumAffected":5,"deathsNumAtRisk":10,"description":"During Phase 1b participants received PD 0360324 50 mg IV Q2W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG015","otherNumAffected":9,"otherNumAtRisk":10,"seriousNumAffected":4,"seriousNumAtRisk":10,"title":"Combination C Phase 1b: PD 0360324 50 mg + Avelumab"},{"deathsNumAffected":4,"deathsNumAtRisk":8,"description":"During Phase 1b participants received PD 0360324 100 mg IV Q2W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG016","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":3,"seriousNumAtRisk":8,"title":"Combination C Phase 1b: PD 0360324 100 mg + Avelumab"},{"deathsNumAffected":4,"deathsNumAtRisk":6,"description":"During Phase 1b participants received PD 0360324 150 mg IV Q2W with 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks.","id":"EG017","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"Combination C Phase 1b: PD 0360324 150 mg + Avelumab"},{"deathsNumAffected":9,"deathsNumAtRisk":12,"description":"During Phase 1b participants received utomilumab 20 mg IV Q4W along with PF-04518600 0.1 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG018","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":2,"seriousNumAtRisk":12,"title":"Combination D Phase 1b: Utomilumab 20 mg + PF-04518600 0.1 mg/kg + Avelumab"},{"deathsNumAffected":7,"deathsNumAtRisk":12,"description":"During Phase 1b participants received utomilumab 50 mg IV Q4W along with PF-04518600 0.1 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG019","otherNumAffected":11,"otherNumAtRisk":12,"seriousNumAffected":3,"seriousNumAtRisk":12,"title":"Combination D Phase 1b: Utomilumab 50 mg + PF-04518600 0.1 mg/kg + Avelumab"},{"deathsNumAffected":7,"deathsNumAtRisk":12,"description":"During Phase 1b participants received utomilumab 20 mg IV Q4W along with PF-04518600 0.3 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG020","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":4,"seriousNumAtRisk":12,"title":"Combination D Phase 1b: Utomilumab 20 mg + PF-04518600 0.3 mg/kg + Avelumab"},{"deathsNumAffected":8,"deathsNumAtRisk":12,"description":"During Phase 1b participants received utomilumab 50 mg IV Q4W along with PF-04518600 0.3 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG021","otherNumAffected":11,"otherNumAtRisk":12,"seriousNumAffected":5,"seriousNumAtRisk":12,"title":"Combination D Phase 1b: Utomilumab 50 mg + PF-04518600 0.3 mg/kg + Avelumab"},{"deathsNumAffected":10,"deathsNumAtRisk":12,"description":"During Phase 1b participants received utomilumab 20 mg IV Q4W along with PF-04518600 1.0 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG022","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":4,"seriousNumAtRisk":12,"title":"Combination D Phase 1b: Utomilumab 20 mg + PF-04518600 1.0 mg/kg + Avelumab"},{"deathsNumAffected":7,"deathsNumAtRisk":11,"description":"During Phase 1b participants received utomilumab 50 mg IV Q4W along with PF-04518600 1.0 mg/kg IV Q2W and 10 mg/kg of avelumab administered IV Q2W for 2 cycles, where each cycle was of 4 weeks. Phase 2 was not planned.","id":"EG023","otherNumAffected":11,"otherNumAtRisk":11,"seriousNumAffected":5,"seriousNumAtRisk":11,"title":"Combination D Phase 1b: Utomilumab 50 mg + PF-04518600 1.0 mg/kg + Avelumab"},{"deathsNumAffected":4,"deathsNumAtRisk":6,"description":"During Phase 1b participants with SCCHN received CMP-001 at 10 mg for an initial 7 doses (2 sub-cutaneous \\[SC\\] administered at weekly intervals, followed by 5 intra tumoral \\[IT\\] administered at weekly intervals) and then administered IT Q2W for all cohorts along with 10 mg/kg of avelumab administered IV Q2W. Phase 2 was not planned.","id":"EG024","otherNumAffected":5,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"Combination F Phase 1b SCCHN: CMP-001 10 mg + Avelumab"},{"deathsNumAffected":5,"deathsNumAtRisk":7,"description":"During Phase 1b participants with SCCHN received CMP-001 at 10 mg for an initial 7 doses (2 SC administered at weekly intervals, followed by 5 IT administered at weekly intervals) and then administered IT Q2W for all cohorts along with 10 mg/kg of avelumab administered IV Q2W all cohorts plus utomilumab 100 mg administered IV Q4W. Phase 2 was not planned.","id":"EG025","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":4,"seriousNumAtRisk":7,"title":"Combination F Phase 1b SCCHN: CMP-001 10 mg Then Avelumab + Utomilumab 100 mg"},{"deathsNumAffected":7,"deathsNumAtRisk":7,"description":"During Phase 1b participants with SCCHN received CMP-001 at 10 mg for an initial 7 doses (2 SC administered at weekly intervals, followed by 5 IT administered at weekly intervals) and then administered IT Q2W for all cohorts along with 10 mg/kg of avelumab administered IV Q2W all cohorts plus PF-04518600 at 0.3 mg/kg administered IV Q2W. Phase 2 was not planned.","id":"EG026","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":4,"seriousNumAtRisk":7,"title":"Combination F Phase 1b SCCHN: CMP-001 10 mg Then Avelumab + PF-04518600 0.3 mg/kg"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v25.0","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":29},{"groupId":"EG001","numAffected":4,"numAtRisk":27},{"groupId":"EG002","numAffected":1,"numAtRisk":29},{"groupId":"EG003","numAffected":1,"numAtRisk":28},{"groupId":"EG004","numAffected":6,"numAtRisk":35},{"groupId":"EG005","numAffected":2,"numAtRisk":21},{"groupId":"EG006","numAffected":1,"numAtRisk":10},{"groupId":"EG007","numAffected":2,"numAtRisk":21},{"groupId":"EG008","numAffected":1,"numAtRisk":11},{"groupId":"EG009","numAffected":3,"numAtRisk":11},{"groupId":"EG010","numAffected":1,"numAtRisk":12},{"groupId":"EG011","numAffected":3,"numAtRisk":12},{"groupId":"EG012","numAffected":1,"numAtRisk":8},{"groupId":"EG013","numAffected":2,"numAtRisk":14},{"groupId":"EG014","numAffected":1,"numAtRisk":25},{"groupId":"EG015","numAffected":1,"numAtRisk":10},{"groupId":"EG016","numAffected":1,"numAtRisk":8},{"groupId":"EG017","numAffected":0,"numAtRisk":6},{"groupId":"EG018","numAffected":2,"numAtRisk":12},{"groupId":"EG019","numAffected":1,"numAtRisk":12},{"groupId":"EG020","numAffected":2,"numAtRisk":12},{"groupId":"EG021","numAffected":2,"numAtRisk":12},{"groupId":"EG022","numAffected":1,"numAtRisk":12},{"groupId":"EG023","numAffected":2,"numAtRisk":11},{"groupId":"EG024","numAffected":1,"numAtRisk":6},{"groupId":"EG025","numAffected":2,"numAtRisk":7},{"groupId":"EG026","numAffected":3,"numAtRisk":7}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v25.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":29},{"groupId":"EG001","numAffected":0,"numAtRisk":27},{"groupId":"EG002","numAffected":0,"numAtRisk":29},{"groupId":"EG003","numAffected":0,"numAtRisk":28},{"groupId":"EG004","numAffected":0,"numAtRisk":35},{"groupId":"EG005","numAffected":1,"numAtRisk":21},{"groupId":"EG006","numAffected":1,"numAtRisk":10},{"groupId":"EG007","numAffected":1,"numAtRisk":21},{"groupId":"EG008","numAffected":0,"numAtRisk":11},{"groupId":"EG009","numAffected":0,"numAtRisk":11},{"groupId":"EG010","numAffected":0,"numAtRisk":12},{"groupId":"EG011","numAffected":0,"numAtRisk":12},{"groupId":"EG012","numAffected":0,"numAtRisk":8},{"groupId":"EG013","numAffected":0,"numAtRisk":14},{"groupId":"EG014","numAffected":0,"numAtRisk":25},{"groupId":"EG015","numAffected":0,"numAtRisk":10},{"groupId":"EG016","numAffected":0,"numAtRisk":8},{"groupId":"EG017","numAffected":0,"numAtRisk":6},{"groupId":"EG018","numAffected":0,"numAtRisk":12},{"groupId":"EG019","numAffected":0,"numAtRisk":12},{"groupId":"EG020","numAffected":0,"numAtRisk":12},{"groupId":"EG021","numAffected":0,"numAtRisk":12},{"groupId":"EG022","numAffected":0,"numAtRisk":12},{"groupId":"EG023","numAffected":0,"numAtRisk":11},{"groupId":"EG024","numAffected":0,"numAtRisk":6},{"groupId":"EG025","numAffected":0,"numAtRisk":7},{"groupId":"EG026","numAffected":0,"numAtRisk":7}],"term":"Increased tendency to bruise"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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deficiency anaemia"},{"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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