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Phase IIIB, Open-label, Multi-Center Study of the Efficacy and Safety of Rigosertib Administered as 72-hour Continuous Intravenous Infusions in Patients With Myelodysplastic Syndrome With Excess Blasts Progressing On or After Azacitidine or Decitabine

Trial Profile

Phase IIIB, Open-label, Multi-Center Study of the Efficacy and Safety of Rigosertib Administered as 72-hour Continuous Intravenous Infusions in Patients With Myelodysplastic Syndrome With Excess Blasts Progressing On or After Azacitidine or Decitabine

Status: Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 17 Dec 2018

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At a glance

  • Drugs Rigosertib (Primary)
  • Indications Chronic myelomonocytic leukaemia; Myelodysplastic syndromes
  • Focus Registrational; Therapeutic Use
  • Sponsors Onconova Therapeutics
  • Most Recent Events

    • 12 Dec 2018 This trial has been completed in Italy (end date: 2017-06-29)
    • 31 Aug 2018 Biomarkers information updated
    • 20 Jul 2018 Planned End Date changed from 1 Nov 2018 to 1 Feb 2019.
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