{"denomUnitsSelected":"Participants","description":"An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. The number of participants who discontinue study treatment due to an AE will be reported for Arms 1 and 2.","reportingStatus":"NOT_POSTED","timeFrame":"Up to approximately 28 months","title":"Number of Participants Who Discontinued Study Treatment Due to an Adverse Event (AE)","type":"SECONDARY"}