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Of the 26 participants who were considered in placebo for safety, 10 died and hence are shown in the placebo arm.","eventGroups":[{"deathsNumAffected":0,"deathsNumAtRisk":232,"description":"Participants received vemurafenib, 960 mg (four, 240 mg tablets) PO, BID along with cobimetinib 60 mg (three, 20 mg tablets) PO, QD on Days 1 to 21 only followed by vemurafenib 720 mg (three, 240 mg tablets) PO, BID and vemurafenib matching placebo, PO, BID on Days 22 to 28 during the 28 day run-in period.","id":"EG000","otherNumAffected":208,"otherNumAtRisk":232,"seriousNumAffected":21,"seriousNumAtRisk":232,"title":"Run-in - Atezo + Cobi + Vem"},{"deathsNumAffected":25,"deathsNumAtRisk":279,"description":"Participants received vemurafenib, 960 mg (four, 240 mg tablets), PO, BID along with cobimetinib, 60 mg (three, 20 mg tablets) PO, QD on Days 1 to 21 only followed by vemurafenib 960 mg (four, 240 mg tablets), PO, BID on Days 22 to 28 during the 28 day run-in period.","id":"EG001","otherNumAffected":262,"otherNumAtRisk":279,"seriousNumAffected":50,"seriousNumAtRisk":279,"title":"Run-in - Pbo + Cobi + Vem"},{"deathsNumAffected":149,"deathsNumAtRisk":279,"description":"After the 28-day run-in, participants received atezolizumab matching placebo as IV infusion on Days 1 and 15, cobimetinib, 60 mg (three, 20 mg tablets) PO, QD, on Days 1 to 21 and vemurafenib 960 mg (four, 240 mg tablets) PO, BID on Days 1 to 28. Study treatment was continued until investigator determined PD, death, unacceptable toxicity, withdrawal of consent, or pregnancy, whichever occurred first.","id":"EG002","otherNumAffected":222,"otherNumAtRisk":279,"seriousNumAffected":81,"seriousNumAtRisk":279,"title":"Triple Combination: Pbo + Cobi + Vem"},{"deathsNumAffected":128,"deathsNumAtRisk":232,"description":"After the 28-day run-in period, participants received atezolizumab 840 mg as IV infusion on Days 1 and 15, cobimetinib, 60 mg (three, 20 mg tablets) PO, QD, on Days 1 to 21, vemurafenib 720 mg (three, 240 mg tablets) PO BID on Days 1 to 28, and vemurafenib placebo (1 tablet) PO BID on Days 1 to 28. Study treatment was continued until investigator determined PD, death, unacceptable toxicity, withdrawal of consent, or pregnancy, whichever occurred first.","id":"EG003","otherNumAffected":226,"otherNumAtRisk":232,"seriousNumAffected":109,"seriousNumAtRisk":232,"title":"Triple Combination: Atezo + Cobi + Vem"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 27.0","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":232,"numEvents":3},{"groupId":"EG001","numAffected":9,"numAtRisk":279,"numEvents":11},{"groupId":"EG002","numAffected":37,"numAtRisk":279,"numEvents":62},{"groupId":"EG003","numAffected":44,"numAtRisk":232,"numEvents":78}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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