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All participants continued their double-blind treatment until LPI+18 months.\n\nAll participants had the option to enter into the OLEP, where they continued to receive CAEL-101 in addition to any SoC prescribed by a physician.","id":"EG001","otherNumAffected":37,"otherNumAtRisk":40,"seriousNumAffected":33,"seriousNumAtRisk":40,"title":"Placebo + Plasma Cell Dyscrasia Treatment"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":21,"numAtRisk":84},{"groupId":"EG001","numAffected":11,"numAtRisk":40}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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Alkaline Phosphatase Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":6,"numAtRisk":84},{"groupId":"EG001","numAffected":0,"numAtRisk":40}],"term":"Aspartate Aminotransferase Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":84},{"groupId":"EG001","numAffected":3,"numAtRisk":40}],"term":"Weight Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":84},{"groupId":"EG001","numAffected":3,"numAtRisk":40}],"term":"Lymphocyte Count Decreased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 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