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After completion of the treatment period, participants returned to the study site monthly for follow-up assessments for an additional 3 months (i.e., Days 113, 141, and 169)","id":"EG001","otherNumAffected":7,"otherNumAtRisk":8,"seriousNumAffected":0,"seriousNumAtRisk":8,"title":"ACE 011 0.3 mg/kg"},{"deathsNumAffected":0,"deathsNumAtRisk":8,"description":"0.5 mg/kg administered via subcutaneous injection every 28 days for a total of four doses (i.e., Days 1, 29, 57, and 85), with safety follow-up visits 1 week after each dose (i.e., Days 8, 36, 64, and 92). After completion of the treatment period, participants returned to the study site monthly for follow-up assessments for an additional 3 months (i.e., Days 113, 141, and 169).","id":"EG002","otherNumAffected":8,"otherNumAtRisk":8,"seriousNumAffected":3,"seriousNumAtRisk":8,"title":"ACE 011 0.5 mg/kg"},{"deathsNumAffected":0,"deathsNumAtRisk":6,"description":"Placebo was administered within 28 days of screening. Subsequent doses were administered every 28 days for a total of four doses.","id":"EG003","otherNumAffected":4,"otherNumAtRisk":6,"seriousNumAffected":0,"seriousNumAtRisk":6,"title":"Placebo"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"11.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":8},{"groupId":"EG001","numAffected":1,"numAtRisk":8},{"groupId":"EG002","numAffected":2,"numAtRisk":8},{"groupId":"EG003","numAffected":0,"numAtRisk":6}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"11.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":8},{"groupId":"EG001","numAffected":0,"numAtRisk":8},{"groupId":"EG002","numAffected":0,"numAtRisk":8},{"groupId":"EG003","numAffected":1,"numAtRisk":6}],"term":"Eosinophilia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood 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SAEs and Other AEs were assessed from first dose to Day 169."}