The goal of this clinical trial is to compare the safety and efficacy of belantamab mafodotin combinated with lenalidomide and dexamethasone to the combination of daratumumab, lenalidomide and dexamethasone in participants who have newly diagnosed multiple myeloma and are not eligible for autologous stem cell transplantation.
This trial is currently open and accepting patients.
In DREAMM-10, the study drug (belantamab mafodotin) will be combined with 2 drugs already approved to treat multiple myeloma, lenalidomide and dexamethasone. Everyone in the study will take these 2 standard drugs, but some will also take, daratumumab, instead of belantamab mafodotin. Daratumumab, also approved for multiple myeloma, will serve as the ‘control’, which means the study drug (belantamab mafodotin) will be compared to it.
After screening to check if DREAMM-10 is a good fit, participants will be randomly assigned (as if by the flip of a coin, or a 50/50 chance) To 1 of the 2 treatment “arms” (groups).
Depending on your treatment arm, you will get intravenous (IV, through a vein in your arm) treatment or subcutaneous injection (needle beneath the skin). Both groups will also take capsules and tablets by mouth.
You may continue to receive treatment unless your multiple myeloma gets worse or you have unwanted side effects or choose to discontinue participation.
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.
Phase 3
Enrollment: 520 patients (estimated)
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Ann Arbor, MI
Hackensack, NJ
Tacoma, WA
Washington, DC
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