{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"2"},{"groupId":"OG001","value":"3"},{"groupId":"OG002","value":"0"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"3"},{"groupId":"OG001","value":"3"},{"groupId":"OG002","value":"3"}],"units":"Participants"}],"description":"Number of patients with Stable Disease greater than or equal to 90 days","groups":[{"description":"Patients receive 20 mg leflunomide PO QD on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.","id":"OG000","title":"Arm 1: 20 mg Leflunomide"},{"description":"Patients receive 40 mg leflunomide PO QD on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.","id":"OG001","title":"Arm 2: 40 mg Leflunomide"},{"description":"Patients receive 60 mg leflunomide PO QD on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.","id":"OG002","title":"Arm 3: 60 mg Leflunomide"}],"paramType":"COUNT_OF_PARTICIPANTS","populationDescription":"Nine patients who reached CR among 11 patients evaluable for response. Because we obtained preclinical data indicating a synergistic effect between leflunomide and lenalidomide, we determined that investigating leflunomide-based combinational therapy was favorable over pursuing a phase 2 study of single-agent leflunomide. There were no dose de-escalations, so there were no patients accrued to the arms for 10mg, 30mg, or 50mg.","reportingStatus":"POSTED","timeFrame":"Assessed at ninety days.","title":"Response Duration","type":"SECONDARY","unitOfMeasure":"Participants"}