{"anticipatedPostingDate":"2028-08","denomUnitsSelected":"Participants","description":"An AE is any untoward medical occurrence in a participant when administered a pharmaceutical product regardless of the causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom/disease temporally associated with the use of an investigational product, whether or not considered related to the investigational product.","reportingStatus":"NOT_POSTED","timeFrame":"Up to 12 years","title":"Percentage of Participants With Adverse Events (AEs)","type":"SECONDARY"}