{"anticipatedPostingDate":"2027-12","denomUnitsSelected":"Participants","description":"An AE was any untoward medical occurrence in clinical study participant temporally associated with use of study intervention, whether or not considered related to study intervention. AEs were graded according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version (v) 4.03 where grade 1= mild, grade 2= moderate, grade 3= severe, grade 4= life-threatening and grade 5= death related to AE. In this outcome measure, number of participants with grade 3 or 4 AEs and grade 5 AEs were reported.","reportingStatus":"NOT_POSTED","timeFrame":"Through end of the study","title":"SLI: Number of Participants With Grade 3 or 4 AEs and Grade 5 AEs","type":"SECONDARY"}