{"anticipatedPostingDate":"2031-09","denomUnitsSelected":"Participants","description":"An AE is an untoward medical occurrence in participant administered a pharmaceutical product \\& regardless of causal relationship with this treatment. An AE can therefore be any unfavorable \\& unintended sign (including an abnormal laboratory finding), symptom/disease temporally associated with use of investigational product, whether or not considered related to investigational product.","reportingStatus":"NOT_POSTED","timeFrame":"Up to approximately 6 years","title":"Number of Participants With Adverse Events (AEs)","type":"SECONDARY"}