The purpose of this study is to test whether giving high doses of carfilzomib along with the other drugs (lenalidomide and dexamethasone) is safe and which dose is best tolerated by patients. In addition, the study is designed to test the amount of remaining myeloma cells in the body after treatment with higher carfilzomib doses which is known as minimal residual disease (MRD).
SparkCures ID | 841 |
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Trial Phase | Phase 1/2 |
Enrollment | 25 Patients |
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NCT Identifier |
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The following criteria is a partial list of reasons why patients may or may not be eligible to participate in this clinical trial. Further evaluation with a medical professional will be required to determine full eligibility.
The following criteria is provided for health care professionals.
Inclusion Criteria:
Exclusion Criteria:
Patients receiving >1 cycle of prior treatment or concurrent systemic treatment for multiple myeloma.
Please visit the ClinicalTrials.gov page for historical site information.
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