{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"0.975","upperLimit":"1.73","value":"1.46"}]}],"title":"Cycle 1, Day 16"},{"categories":[{"measurements":[{"groupId":"OG000","lowerLimit":"0.903","upperLimit":"1.70","value":"1.10"}]}],"title":"Cycle 2, Day 1"}],"denoms":[{"counts":[{"groupId":"OG000","value":"10"},{"groupId":"OG001","value":"0"}],"units":"Participants"}],"dispersionType":"Full Range","groups":[{"description":"Participants with normal renal function received carfilzomib 20 mg/m² IV on days 1 and 2 of cycle 1, followed by 27 mg/m² IV on days 8, 9, 15, and 16 of cycle 1. Participants who adequately tolerated dosing at 27 mg/m² received carfilzomib 56 mg/m² IV on days 1, 2, 8, 9, 15 and 16 of cycle 2 and all subsequent cycles.","id":"OG000","title":"Normal Renal Function"},{"description":"Participants with ESRD received carfilzomib 20 mg/m² IV on days 1 and 2 of cycle 1, followed by 27 mg/m² IV on days 8, 9, 15, and 16 of cycle 1. Participants who adequately tolerated dosing at 27 mg/m² received carfilzomib 56 mg/m² IV on days 1, 2, 8, 9, 15 and 16 of cycle 2 and all subsequent cycles.","id":"OG001","title":"End Stage Renal Disease"}],"paramType":"MEDIAN","populationDescription":"PK evaluable population. Participants for whom the extrapolated portion of AUC0-∞ was \\> 20% were excluded. T½ could not be calculated for the ESRD group as the extrapolated portion (AUCextr) was greater than 20% in all participants.","reportingStatus":"POSTED","timeFrame":"Cycle 1, day 16 and cycle 2, day 1 at predose, 15 minutes post start of infusion, immediately before the end of infusion, and at 5, 15, and 30 minutes, and 1, 2, and 4 hours after the end of the infusion.","title":"Terminal Half-life (T½) of Metabolite PR-389/M14","type":"SECONDARY","unitOfMeasure":"hours"}