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A Phase 1/2, Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BMS-863233 in Subjects With Refractory Hematologic Malignancies

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Trial Profile

A Phase 1/2, Multiple Ascending Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BMS-863233 in Subjects With Refractory Hematologic Malignancies

Status: Discontinued
Phase of Trial: Phase I/II

Latest Information Update: 09 Nov 2021

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At a glance

  • Drugs XL 413 (Primary)
  • Indications Acute myeloid leukaemia; Chronic myeloid leukaemia; Haematological malignancies; Myelodysplastic syndromes; Precursor cell lymphoblastic leukaemia-lymphoma
  • Focus Adverse reactions
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 11 Aug 2010 Status changed from suspended to discontinued as reported by ClinicalTrials.gov.
    • 21 May 2010 Planned end date changed from 1 Jul 2011 to 1 Nov 2012 as reported by ClinicalTrials.gov.
    • 01 May 2010 Status changed from recruiting to suspended as reported by ClinicalTrials.gov.

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