{"denomUnitsSelected":"Participants","description":"The number of induction or consolidation reporting periods in which a CTC version 4 codeable non-hematological adverse event, grade 3 left ventricular systolic dysfunction or the reporting period is terminated because of a CTC codeable event.","reportingStatus":"NOT_POSTED","timeFrame":"Up to 307 days","title":"Frequency of Toxicity Events During Ganitumab Maintenance","type":"OTHER_PRE_SPECIFIED"}