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Participants were continued to receive niraparib 200 mg and abiraterone acetate 1000 mg plus prednisone 10 mg in the open label extension phase.","id":"EG000","otherNumAffected":198,"otherNumAtRisk":212,"seriousNumAffected":76,"seriousNumAtRisk":212,"title":"Cohort 1: Niraparib 200 mg + Abiraterone Acetate 1000 mg + Prednisone 10 mg"},{"deathsNumAffected":59,"deathsNumAtRisk":211,"description":"Participants with mCRPC and positive HRR gene alteration, received placebo in combination with abiraterone acetate 1000 mg tablet orally QD and prednisone 5 mg tablet orally BID (total dose 10 mg) in each 28 days treatment cycle starting from Cycle 1 Day 1 up to 29 months. Participants were then followed up for safety up to 5 years after last dose or until death, loss to follow-up, withdrawal of consent, or study termination. Participants who received placebo and abiraterone acetate plus prednisone were allowed to cross over to receive niraparib 200 mg and abiraterone acetate 1000 mg plus prednisone 10 mg in the open-label extension phase.","id":"EG001","otherNumAffected":178,"otherNumAtRisk":211,"seriousNumAffected":52,"seriousNumAtRisk":211,"title":"Cohort 1: Placebo + Abiraterone Acetate 1000 mg + Prednisone 10 mg"},{"deathsNumAffected":53,"deathsNumAtRisk":123,"description":"Participants with mCRPC and negative HRR gene alteration, received niraparib 200 mg capsule in combination with abiraterone acetate 1000 mg tablet orally QD and prednisone 5 mg tablet orally BID (total dose 10 mg) in each 28 days treatment cycle starting from Cycle 1 Day 1 up to 29 months. Participants were then followed up for safety up to 5 years after last dose or until death, loss to follow-up, withdrawal of consent, or study termination. Participants were continued to receive niraparib 200 mg and abiraterone acetate 1000 mg plus prednisone 10 mg in the open label extension phase.","id":"EG002","otherNumAffected":117,"otherNumAtRisk":123,"seriousNumAffected":66,"seriousNumAtRisk":123,"title":"Cohort 2: Niraparib 200 mg + Abiraterone Acetate 1000 mg + Prednisone 10 mg"},{"deathsNumAffected":44,"deathsNumAtRisk":123,"description":"Participants with mCRPC and negative HRR gene alteration, received placebo in combination with abiraterone acetate 1000 mg tablet orally QD and prednisone 5 mg tablet orally BID (total dose 10 mg) in each 28 days treatment cycle starting from Cycle 1 Day 1 up to 29 months. Participants were then followed up for safety up to 5 years after last dose or until death, loss to follow-up, withdrawal of consent, or study termination. Participants who received placebo and abiraterone acetate plus prednisone were allowed to cross over to receive niraparib 200 mg and abiraterone acetate 1000 mg plus prednisone 10 mg in the open-label extension phase.","id":"EG003","otherNumAffected":108,"otherNumAtRisk":123,"seriousNumAffected":45,"seriousNumAtRisk":123,"title":"Cohort 2: Placebo + Abiraterone Acetate 1000 mg + Prednisone 10 mg"},{"deathsNumAffected":9,"deathsNumAtRisk":95,"description":"Participants with mCRPC and positive HRR gene alteration, received fixed-dose combination (FDC) of niraparib 200 mg and abiraterone acetate 1000 mg combination tablet orally QD with prednisone 5 mg tablet orally BID (total dose 10 mg) in each 28 days treatment cycle starting from Cycle 1 Day 1 up to 9 months. Participants were then followed up for safety up to 5 years after last dose or until death, loss to follow-up, withdrawal of consent, or study termination. Participants were continued to receive same treatment in long-term extension phase.","id":"EG004","otherNumAffected":83,"otherNumAtRisk":95,"seriousNumAffected":21,"seriousNumAtRisk":95,"title":"Cohort 3: Niraparib 200 mg and Abiraterone Acetate 1000 mg FDC + Prednisone 10 mg"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 24.0","stats":[{"groupId":"EG000","numAffected":95,"numAtRisk":212},{"groupId":"EG001","numAffected":43,"numAtRisk":211},{"groupId":"EG002","numAffected":59,"numAtRisk":123},{"groupId":"EG003","numAffected":19,"numAtRisk":123},{"groupId":"EG004","numAffected":37,"numAtRisk":95}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 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