{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"0"}]}],"title":"AEs occurring between leukapheresis and lymphodepleting chemotherapy (LDC)"},{"categories":[{"measurements":[{"groupId":"OG000","value":"2"}]}],"title":"AEs occurring between LDC and JCAR017 infusion"},{"categories":[{"measurements":[{"groupId":"OG000","value":"9"}]}],"title":"AEs occurring between JCAR017 infusion and Day 30"},{"categories":[{"measurements":[{"groupId":"OG000","value":"7"}]}],"title":"AEs occurring between Day 31 and Day 90"},{"categories":[{"measurements":[{"groupId":"OG000","value":"7"}]}],"title":"AEs occurring between Day 91 and end of study"}],"denoms":[{"counts":[{"groupId":"OG000","value":"9"}],"units":"Participants"}],"description":"An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.","groups":[{"description":"JCAR017 was infused at a dose of 100 x 10\\^6 JCAR017-positive transfected viable T cells (50 × 10\\^6 CD8+ CAR+ T cells and 50 × 10\\^6 CD4+ CAR+ T cells), on Day 1 (2 to 7 days after completion of Lymphodepleting chemotherapy).","id":"OG000","title":"Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting"}],"paramType":"COUNT_OF_PARTICIPANTS","populationDescription":"All participants in the JCAR017 treated set. Prespecified to be reported for cohort 7 only","reportingStatus":"POSTED","timeFrame":"From leukapheresis to end of study (up to approximately 63 months)","title":"Number of Participants With Adverse Events in Cohort 7","type":"PRIMARY","unitOfMeasure":"Participants"}