{"anticipatedPostingDate":"2027-06","denomUnitsSelected":"Participants","description":"An AE is any untoward medical occurrence in a clinical study participant, temporally associated with the use of a study treatment, whether or not considered related to the study treatment. AEs will be coded using the Medical Dictionary for Regulatory Activities (MedDRA dictionary).","reportingStatus":"NOT_POSTED","timeFrame":"Up to 255 weeks","title":"Number of Participants With Adverse Events (AEs)","type":"SECONDARY"}