{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"18","value":"1.23"},{"groupId":"OG001","spread":"16","value":"1.25"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"97"},{"groupId":"OG001","value":"18"}],"units":"Participants"}],"description":"Accumulation ratio is AUCtau following administration in Cycle 2 / AUCtau after administration in Cycle 1","dispersionType":"Geometric Coefficient of Variation","groups":[{"description":"Includes participants from all treatment arms that were administered AMG 820 1100 mg.","id":"OG000","title":"AMG 820 1100 mg"},{"description":"Includes participants from all treatment arms who were administered AMG 820 1400 mg","id":"OG001","title":"AMG 820 1400 mg"}],"paramType":"GEOMETRIC_MEAN","populationDescription":"Pharmacovigilence Analysis Set contains all participants who received at least 1 dose of AMG 820 and have at least one PK sample collected.","reportingStatus":"POSTED","timeFrame":"Cycle 1, Study Day 1: pre-infusion, at end of infusion, hours 1, 6 and 24 post infusion, Days 5, 8 and 15. Cycle 2, Study Day 22: pre-infusion, at end of infusion, hours 1, 6, 24 post infusion, Days 26, 29 and 36","title":"AMG 820 Pharmacokinetic Parameter by Dose Group: Accumulation Ratio (AR)","type":"SECONDARY","unitOfMeasure":"ratio"}