{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","spread":"1.0","value":"1.8"},{"groupId":"OG001","spread":"1.1","value":"1.8"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"27"},{"groupId":"OG001","value":"27"}],"units":"Participants"}],"description":"Time from randomization to the date of the first documented confirmed response in a patient who has responded with ≥PR.","dispersionType":"Standard Deviation","groups":[{"description":"Treatment was given in 28-day cycles in an outpatient treatment setting.\n\n* Melflufen 30 mg intravenous (i.v.) infusion on Day 1 of each cycle\n* Dexamethasone 40 mg per oral (p.o.) weekly (20 mg p.o. weekly if ≥75 years)\n* Daratumumab 1800 mg subcutaneously (s.c.) on Days 1, 8, 15, and 22 in Cycles 1 and 2, on Days 1 and 15 in Cycles 3 to 6, and on Day 1 from Cycle 7","id":"OG000","title":"Arm A (Melflufen+Dexamethasone+Daratumumab)"},{"description":"Treatment was given in 28-day cycles in an outpatient treatment setting.\n\n• Daratumumab 1800 mg s.c. on Days 1, 8, 15, and 22 in Cycles 1 and 2, on Days 1 and 15 in Cycles 3 to 6, and on Day 1 from Cycle 7","id":"OG001","title":"Arm B (Daratumumab)"}],"paramType":"MEAN","populationDescription":"Analysis was performed using the Full Analysis Set (FAS).","reportingStatus":"POSTED","timeFrame":"From the date of randomization until the end of study (approximately 12 months).","title":"Time to Response (TTR)","type":"SECONDARY","unitOfMeasure":"months"}