{"description":"The safety population did not include 2 patients (one on MMB and one on RUX) who were not dosed, hence affecting the total number of patients at risk.","eventGroups":[{"deathsNumAffected":8,"deathsNumAtRisk":214,"description":"Participants received momelotinib plus placebo to match ruxolitinib.\n\nMomelotinib tablets were administered orally once daily at a starting dose of 200 mg.\n\nAdditional available strengths included 100 mg and 150 mg. Placebo to match ruxolitinib tablets were administered orally twice daily.","id":"EG000","otherNumAffected":197,"otherNumAtRisk":214,"seriousNumAffected":49,"seriousNumAtRisk":214,"title":"Momelotinib (MMB)"},{"deathsNumAffected":6,"deathsNumAtRisk":216,"description":"Participants received ruxolitinib plus placebo to match momelotinib.\n\nRuxolitinib tablets were administered orally twice daily. The dose ranged from 5 to 20 mg BID and was dependent on platelet count, creatinine clearance, and transaminase levels.\n\nPlacebo to match momelotinib tablets were administered orally once daily.","id":"EG001","otherNumAffected":206,"otherNumAtRisk":216,"seriousNumAffected":39,"seriousNumAtRisk":216,"title":"Ruxolitinib (RUX)"},{"deathsNumAffected":44,"deathsNumAtRisk":171,"description":"After completion of the 24-week double-blind treatment phase, participants had the option to receive MMB in an open-label treatment phase for up to an additional 216 weeks. Participants randomized to the MMB group at study entry continued MMB in the open-label treatment phase at their current dose. Available MMB strengths were 100 mg, 150 mg and 200 mg.","id":"EG002","otherNumAffected":153,"otherNumAtRisk":171,"seriousNumAffected":79,"seriousNumAtRisk":171,"title":"MMB to MMB"},{"deathsNumAffected":54,"deathsNumAtRisk":197,"description":"After completion of the 24-week double-blind treatment phase, participants had the option to receive MMB in an open-label treatment phase for up to an additional 216 weeks. Participants randomized to the RUX group who wished to remain in the study initiated MMB in the open-label treatment phase at the dose matching their equivalent MMB placebo dose. Available MMB strengths were 100 mg, 150 mg and 200 mg.","id":"EG003","otherNumAffected":188,"otherNumAtRisk":197,"seriousNumAffected":79,"seriousNumAtRisk":197,"title":"RUX to MMB"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":21,"numAtRisk":214},{"groupId":"EG001","numAffected":24,"numAtRisk":216},{"groupId":"EG002","numAffected":13,"numAtRisk":171},{"groupId":"EG003","numAffected":26,"numAtRisk":197}],"term":"Abdominal pain"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":214},{"groupId":"EG001","numAffected":10,"numAtRisk":216},{"groupId":"EG002","numAffected":5,"numAtRisk":171},{"groupId":"EG003","numAffected":11,"numAtRisk":197}],"term":"Alanine aminotransferase increased"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":30,"numAtRisk":214},{"groupId":"EG001","numAffected":79,"numAtRisk":216},{"groupId":"EG002","numAffected":38,"numAtRisk":171},{"groupId":"EG003","numAffected":29,"numAtRisk":197}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Musculoskeletal and connective tissue disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":15,"numAtRisk":214},{"groupId":"EG001","numAffected":10,"numAtRisk":216},{"groupId":"EG002","numAffected":10,"numAtRisk":171},{"groupId":"EG003","numAffected":13,"numAtRisk":197}],"term":"Arthralgia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":12,"numAtRisk":214},{"groupId":"EG001","numAffected":16,"numAtRisk":216},{"groupId":"EG002","numAffected":13,"numAtRisk":171},{"groupId":"EG003","numAffected":12,"numAtRisk":197}],"term":"Asthenia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Musculoskeletal and connective tissue disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":214},{"groupId":"EG001","numAffected":10,"numAtRisk":216},{"groupId":"EG002","numAffected":10,"numAtRisk":171},{"groupId":"EG003","numAffected":19,"numAtRisk":197}],"term":"Back pain"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":9,"numAtRisk":214},{"groupId":"EG001","numAffected":2,"numAtRisk":216},{"groupId":"EG002","numAffected":10,"numAtRisk":171},{"groupId":"EG003","numAffected":10,"numAtRisk":197}],"term":"Blood creatinine increased"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Musculoskeletal and connective tissue disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":214},{"groupId":"EG001","numAffected":15,"numAtRisk":216},{"groupId":"EG002","numAffected":4,"numAtRisk":171},{"groupId":"EG003","numAffected":12,"numAtRisk":197}],"term":"Bone pain"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":21,"numAtRisk":214},{"groupId":"EG001","numAffected":15,"numAtRisk":216},{"groupId":"EG002","numAffected":13,"numAtRisk":171},{"groupId":"EG003","numAffected":18,"numAtRisk":197}],"term":"Constipation"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Injury, poisoning and procedural complications","sourceVocabulary":"MedDRA 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(22.0)","stats":[{"groupId":"EG000","numAffected":11,"numAtRisk":214},{"groupId":"EG001","numAffected":13,"numAtRisk":216},{"groupId":"EG002","numAffected":15,"numAtRisk":171},{"groupId":"EG003","numAffected":15,"numAtRisk":197}],"term":"Decreased appetite"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":36,"numAtRisk":214},{"groupId":"EG001","numAffected":42,"numAtRisk":216},{"groupId":"EG002","numAffected":30,"numAtRisk":171},{"groupId":"EG003","numAffected":37,"numAtRisk":197}],"term":"Diarrhoea"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Nervous system disorders","sourceVocabulary":"MedDRA 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(22.0)","stats":[{"groupId":"EG000","numAffected":9,"numAtRisk":214},{"groupId":"EG001","numAffected":19,"numAtRisk":216},{"groupId":"EG002","numAffected":10,"numAtRisk":171},{"groupId":"EG003","numAffected":18,"numAtRisk":197}],"term":"Hypertension"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Metabolism and nutrition disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":214},{"groupId":"EG001","numAffected":7,"numAtRisk":216},{"groupId":"EG002","numAffected":11,"numAtRisk":171},{"groupId":"EG003","numAffected":14,"numAtRisk":197}],"term":"Hyperuricaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 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(22.0)","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":214},{"groupId":"EG001","numAffected":11,"numAtRisk":216},{"groupId":"EG002","numAffected":12,"numAtRisk":171},{"groupId":"EG003","numAffected":20,"numAtRisk":197}],"term":"Pruritus"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":12,"numAtRisk":214},{"groupId":"EG001","numAffected":14,"numAtRisk":216},{"groupId":"EG002","numAffected":15,"numAtRisk":171},{"groupId":"EG003","numAffected":14,"numAtRisk":197}],"term":"Pyrexia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":9,"numAtRisk":214},{"groupId":"EG001","numAffected":5,"numAtRisk":216},{"groupId":"EG002","numAffected":10,"numAtRisk":171},{"groupId":"EG003","numAffected":12,"numAtRisk":197}],"term":"Rash"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":40,"numAtRisk":214},{"groupId":"EG001","numAffected":62,"numAtRisk":216},{"groupId":"EG002","numAffected":29,"numAtRisk":171},{"groupId":"EG003","numAffected":39,"numAtRisk":197}],"term":"Thrombocytopenia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Infections and infestations","sourceVocabulary":"MedDRA (22.0)","stats":[{"groupId":"EG000","numAffected":12,"numAtRisk":214},{"groupId":"EG001","numAffected":14,"numAtRisk":216},{"groupId":"EG002","numAffected":18,"numAtRisk":171},{"groupId":"EG003","numAffected":18,"numAtRisk":197}],"term":"Upper respiratory 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