Clinical trial

Decitabine in Treating Patients With Myelodysplastic Syndromes or Acute Myeloid…

NCT00049582 · National Cancer Institute (NCI), NIH · Terminated

Key facts

NCT number NCT00049582
Title Decitabine in Treating Patients With Myelodysplastic Syndromes or Acute Myeloid Leukemia
Official title Phase I Study of 5-Aza-2'-Deoxycytidine (Decitabine) as a Biologic Modifier of Retinoid Responsive Genes in Patients With High-Risk Myelodysplastic Syndromes and Acute Myelogenous Leukemia (De-novo, Relapsed or Secondary)
Lead sponsor National Cancer Institute (NCI), NIH
Status Terminated
Phase Phase 1
Study type Interventional
Conditions Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities, Adult Acute Myeloid Leukemia With Inv(16)(p13, q22), Adult Acute Myeloid Leukemia With t(15, 17)(q22, q12), Adult Acute Myeloid Leukemia With t(16, 16)(p13, Adult Acute Myeloid Leukemia With t(8, 21)(q22 and 10 more
Intervention type Drug, Other
Interventions decitabine, laboratory biomarker analysis, pharmacological study
Enrollment 36
Start date Sep 1, 2002
Primary completion Jun 1, 2010
First posted Jan 27, 2003
Last update posted Sep 30, 2013
Countries Canada

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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