{"description":"All-Cause Mortality is reported for the ITT population. SAEs and AEs were assessed in the Safety Population. After 28 days following last dose of study drug, only SAEs assessed as potentially related to study drug are reported. Events of progression of the participant's underlying cancer, events clearly related to progression of the participant's cancer and progression of disease leading to death are not reported as an AE or SAE.","eventGroups":[{"deathsNumAffected":6,"deathsNumAtRisk":270,"description":"Oral rucaparib (monotherapy).\n\nRucaparib: Rucaparib will be administered daily.","id":"EG000","otherNumAffected":270,"otherNumAtRisk":270,"seriousNumAffected":81,"seriousNumAtRisk":270,"title":"Rucaparib (Treatment Phase)"},{"deathsNumAffected":3,"deathsNumAtRisk":135,"description":"Oral abiraterone acetate (monotherapy, given in combination with prednisone). Oral enzalutamide (monotherapy). 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Participants from the Abiraterone Acetate/Enzalutamide/Docetaxel arm who completed the Treatment Phase and radiographically progressed by independent radiology review (IRR) may receive rucaparib treatment during the Cross-Over Phase.\n\nAfter analysis of the primary endpoint, investigator-assessed radiographic disease progression will be used for cross-over eligibility evaluation.","id":"EG002","otherNumAffected":67,"otherNumAtRisk":70,"seriousNumAffected":18,"seriousNumAtRisk":70,"title":"Rucaparib (Cross-over Phase)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v23.0","stats":[{"groupId":"EG000","numAffected":121,"numAtRisk":270,"numEvents":435},{"groupId":"EG001","numAffected":24,"numAtRisk":130,"numEvents":30},{"groupId":"EG002","numAffected":26,"numAtRisk":70,"numEvents":90}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and 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