The goal of this clinical trial is to learn more about the safety and efficacy of cemsidomide when given in combination with dexamethasone in patients who have relapsed or refractory multiple myeloma.
This trial is currently open and accepting patients.
In this research study, all patients will receive cemsidomide and dexamethasone in cycles. Each cycle in this study will be 28 days (4 weeks).
Patients will take 100 micrograms of cemsidomide by mouth once a day for 14 days, then no cemsidomide for the next 14 days. Patients will also take dexamethasone by mouth once a week. The dose of dexamethasone received depends on the age of the participant.
Patients may continue receiving cemsidomide and dexamethasone until their myeloma gets worse, they have side effects they cannot tolerate, they choose to withdraw from the study, or the study is stopped.
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 2
Enrollment: 100 patients (estimated)
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Iowa City, IA
Ann Arbor, MI
St. Louis, MO
Omaha, NE
Chapel Hill, NC
San Antonio, TX
Madison, WI
We know how difficult and confusing this process can be. If you are interested in this clinical trial or have questions, you can call us at any time. You can also send us a direct message with questions.
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You can explore trial locations from around the US and connect directly with a trial coordinator.
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