{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"662"},{"groupId":"OG001","value":"658"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"662"},{"groupId":"OG001","value":"659"}],"units":"Participants"}],"groups":[{"description":"Brentuximab vedotin 1.2 milligram per kilogram (mg/kg), infusion, intravenously over 30-minutes plus doxorubicin 25 milligram per square meter (mg/m\\^2), vinblastine 6 mg/m\\^2, and dacarbazine 375 mg/m\\^2, infusion, intravenously, once on Days 1 and 15 of each 28-day treatment cycle for up to a maximum of 6 cycles. Brentuximab vedotin was administered within approximately 1 hour after completion of AVD.","id":"OG000","title":"A+AVD"},{"description":"Doxorubicin 25 mg/m\\^2, bleomycin 10 units per square meter (units/m\\^2), vinblastine 6 mg/m\\^2, and dacarbazine 375 mg/m\\^2, infusion, intravenously, once on Days 1 and 15 of each 28-day treatment cycle for up to a maximum of 6 cycles.","id":"OG001","title":"ABVD"}],"paramType":"NUMBER","populationDescription":"The safety population included all enrolled participants who received at least 1 dose of any study drug.","reportingStatus":"POSTED","timeFrame":"Baseline up to 30 days after last dose of study drug (approximately 1 year)","title":"Number of Participants With Abnormal Clinical Laboratory Values","type":"SECONDARY","unitOfMeasure":"participants"}