{"anticipatedPostingDate":"2026-08","denomUnitsSelected":"Participants","description":"An AE is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as AEs.","reportingStatus":"NOT_POSTED","timeFrame":"Up to approximately 10.75 years","title":"Number of Participants With Adverse Events (AEs)","type":"SECONDARY"}