{"denoms":[{"counts":[{"groupId":"OG000","value":"0"}],"units":"Participants"}],"description":"Will be assessed using Tmax for Nivolumab in combination with lenalidomide","groups":[{"description":"Patients receive lenalidomide PO on days 1-21 and nivolumab IV over 1 hour on days 1 and 14. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\nLaboratory Biomarker Analysis: Correlative studies\n\nLenalidomide: Given PO\n\nNivolumab: Given IV\n\nPharmacological Study: Correlative studies","id":"OG000","title":"Treatment (Lenalidomide, Nivolumab)"}],"populationDescription":"data not collected and analyzed","reportingStatus":"POSTED","timeFrame":"Screening, days 1 and 14 of each cycle","title":"Pharmacodynamics Profiles:Time to Maximum Plasma Concentration (Tmax)","type":"OTHER_PRE_SPECIFIED"}