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Participants who subsequently developed independent review committee (IRC)-confirmed progressive disease (PD) and had active disease requiring treatment were eligible to participate in the Subsequent Therapy Phase and received single-agent ibrutinib until disease progression or unacceptable toxicity.","id":"EG000","otherNumAffected":98,"otherNumAtRisk":106,"seriousNumAffected":49,"seriousNumAtRisk":106,"title":"Treatment Arm A (Ibrutinib + Venetoclax)"},{"deathsNumAffected":36,"deathsNumAtRisk":105,"description":"Participants received chlorambucil 0.5 milligrams per kilogram (mg/kg) body weight orally once daily on Days 1 and 15 of Cycles 1 to 6 in combination with obinutuzumab 1000 mgs intravenously (IV) once daily on Days 1, 8, and 15 of Cycle 1 and Day 1 of Cycles 2 to 6 (each cycle is of 28 days). Participants who subsequently developed IRC-confirmed progressive disease (PD) and had active disease requiring treatment were eligible to participate in the Subsequent Therapy Phase and received single-agent ibrutinib until disease progression or unacceptable toxicity.","id":"EG001","otherNumAffected":98,"otherNumAtRisk":105,"seriousNumAffected":30,"seriousNumAtRisk":105,"title":"Treatment Arm B (Chlorambucil + Obinutuzumab)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":17,"numAtRisk":106},{"groupId":"EG001","numAffected":18,"numAtRisk":105}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 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