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27.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":244},{"groupId":"EG001","numAffected":1,"numAtRisk":252}],"term":"Euthanasia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 27.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":244},{"groupId":"EG001","numAffected":1,"numAtRisk":252}],"term":"Aortic aneurysm"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 27.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":244},{"groupId":"EG001","numAffected":1,"numAtRisk":252}],"term":"Circulatory collapse"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 27.1","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":244},{"groupId":"EG001","numAffected":0,"numAtRisk":252}],"term":"Superior vena cava syndrome"}],"timeFrame":"All-cause mortality: from randomization up to primary completion DCO date 29 January 2025; median (min, max) time was 8.6 (0.1, 18.5) months. Adverse events were collected from first dose of drug up to last dose + 65 days up to primary completion DCO date 29 January 2025; median (min, max) time was 5.3 (0.1, 17.3) months."}