25
Participants
Start Date
November 22, 2017
Primary Completion Date
September 29, 2022
Study Completion Date
September 26, 2027
Elotuzumab
During continuation therapy, elotuzumab will be administered on a 28-day cycle as follows: on Days 1 and 15 for Cycles 1-6 and on Day 1 for Cycles 7+. For Cycles 1-6 elotuzumab will be administered intravenously at a dose of 10 mg/kg. For Cycles 7+ elotuzumab will be administered at a dose of 20 mg/kg.
Pomalidomide
During continuation therapy, pomalidomide will be taken by mouth daily on Days 1-21 of each 28-day cycle at a starting dose of 2 mg. During continuation, pomalidomide may be dose escalated to 4 mg at the discretion of the treating physician if the 2 mg dose is tolerated.
Dexamethasone
During continuation therapy, dexamethasone will be taken by mouth at a starting dose of 40 mg. It will be given on a 28-day cycle as follows: on Days 1 and 15 for Cycles 1-6 and on Day 1 only for Cycles 7+. Sufficient quantity of drug for one cycle of therapy will be prescribed to the patient at a time.
Washington University School of Medicine, St Louis
Colorado Blood Cancer Institute (Sarah Cannon), Denver
University Health Network - Princess Margaret Cancer Centre, Toronto
Collaborators (2)
Bristol-Myers Squibb
INDUSTRY
Celgene
INDUSTRY
Washington University School of Medicine
OTHER