{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"18.0","upperLimit":"32.7","value":"24.8"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"145"}],"units":"Participants"}],"description":"CR rate defined as the percentage of treated participants with a best overall response (BOR) of CR.","dispersionType":"95% Confidence Interval","groups":[{"description":"Participants received loncastuximab tesirine as an IV infusion over 30 minutes on Day 1 of each cycle (every 3 weeks) at a dose of 150 μg/kg Q3W for 2 cycles, then 75 μg/kg Q3W for subsequent cycles for up to one year or until disease progression, unacceptable toxicity, or other discontinuation criteria, whichever occurred first.","id":"OG000","title":"Loncastuximab Tesirine"}],"paramType":"NUMBER","populationDescription":"All-treated population - all participants who received at least 1 dose of treatment.","reportingStatus":"POSTED","timeFrame":"Up to 39 months","title":"Complete Response (CR) Rate","type":"SECONDARY","unitOfMeasure":"percentage of participants"}