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Study identifier: NCT04508790 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Leflunomide, Pomalidomide, and Dexamethasone for the Treatment of Relapsed or Refractory Multiple Myeloma

Condition: Recurrent Plasma Cell Myeloma · Refractory Plasma Cell Myeloma  ·  Sponsor: City of Hope Medical Center

PhasePhase 2
Planned participants29
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This phase II trial studies how well leflunomide, pomalidomide, and dexamethasone work for the treatment of multiple myeloma that has come back (relapsed) or does not respond to treatment (refractory). Leflunomide may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Immunotherapy with pomalidomide, may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs, such as dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving leflunomide with pomalidomide and dexamethasone may work better in treating multiple myeloma compared to pomalidomide and dexamethasone alone.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

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Locations (8)

City of Hope Medical CenterDuarte, California, United StatesRecruiting
City of Hope at SeacliffHuntington Beach, California, United StatesRecruiting
City of Hope at Antelope ValleyLancaster, California, United StatesRecruiting
City of Hope at Long Beach ElmLong Beach, California, United StatesRecruiting
City of Hope at Newport Beach Fashion IslandNewport Beach, California, United StatesRecruiting
City of Hope at South PasadenaSouth Pasadena, California, United StatesRecruiting
City of Hope at South BayTorrance, California, United StatesRecruiting
City of Hope at UplandUpland, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04508790