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Study identifier: NCT01928537 Synced from ClinicalTrials.gov · July 28, 2026
● Completed

Efficacy and Safety of IV Rigosertib in MDS Patients With Excess Blasts Progressing After Azacitidine or Decitabine

Condition: Myelodysplastic Syndromes · Refractory Anemia With Excess Blasts · Chronic Myelomonocytic Leukemia  ·  Sponsor: Traws Pharma, Inc.

PhasePhase 3
Planned participants67
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study will examine the effect intravenously administered rigosertib has on the relationship between bone marrow blasts response and overall survival in myelodysplastic syndromes (MDS) patients who have 5-30% bone marrow blasts and who progressed on or after treatment with azacitidine or decitabine.

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 (35)

Stanford University Cancer CenterStanford, California, United States
Rush University Medical CenterChicago, Illinois, United States
University of Chicago MedicineChicago, Illinois, United States
University of Kansas Cancer Center and Medical PavilionWestwood, Kansas, United States
Greenbaum Cancer Center University of MarylandBaltimore, Maryland, United States
Dana Farber Cancer InstituteBoston, Massachusetts, United States
Mayo ClinicRochester, Minnesota, United States
Mount Sinai Medical CenterNew York, New York, United States
Columbia University Medical CenterNew York, New York, United States
New York Presbyterian Hospital-Weill Cornell Medical CollegeNew York, New York, United States
Montefiore Medical CenterThe Bronx, New York, United States
University of Texas Southwestern Medical Center-Parkland HospitalDallas, Texas, United States

+ 23 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT01928537