Clinical trial

Vorinostat and Idarubicin in Treating Patients With Relapsed or Refractory…

NCT00331513 · National Cancer Institute (NCI), NIH · Completed

Key facts

NCT number NCT00331513
Title Vorinostat and Idarubicin in Treating Patients With Relapsed or Refractory Leukemia or Myelodysplastic Syndromes
Official title A Phase 1 Study of Suberoylanilide Hydroxamic Acid (Vorinostat, SAHA) in Combination With Idarubicin in Relapsed or Refractory Leukemia
Lead sponsor National Cancer Institute (NCI), NIH
Status Completed
Phase Phase 1
Study type Interventional
Conditions Acute Myeloid Leukemia With Multilineage Dysplasia Following Myelodysplastic Syndrome, 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 and 11 more
Intervention type Drug, Other
Interventions vorinostat, idarubicin, laboratory biomarker analysis, pharmacological study
Enrollment 40
Start date Mar 1, 2006
Primary completion Jan 1, 2010
First posted May 31, 2006
Last update posted Sep 30, 2013
Countries United States

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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