The purpose of this study is to compare the efficacy and safety of CC-92480, bortezomib and dexamethasone (480Vd) versus pomalidomide, bortezomib and dexamethasone (PVd) in participants with relapsed or refractory multiple myeloma (RRMM) who received between 1 to 3 prior lines of therapy and who have had prior lenalidomide exposure.
This trial is currently open and accepting patients.
The following criteria is a partial list of reasons why patients may be eligible to participate in this clinical trial. Further evaluation with a medical professional is required.
Inclusion Criteria:
Participant has documented diagnosis of MM and measurable disease, defined as any of the following:
Exclusion Criteria:
Other protocol-defined criteria apply.
Phase 3
Enrollment: 760 patients (estimated)
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Iowa City, IA
Ann Arbor, MI
San Antonio, TX
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