Clinical trial

Vorinostat and Decitabine in Treating Patients With Relapsed, Refractory, or…

NCT00357708 · National Cancer Institute (NCI), NIH · Completed

Key facts

NCT number NCT00357708
Title Vorinostat and Decitabine in Treating Patients With Relapsed, Refractory, or Poor-Prognosis Hematologic Cancer or Other Diseases
Official title A Phase I Trial of SAHA (NSC 701852) and Decitabine (IND 50733, NSC 127716) in Patients With Relapsed, Refractory or Poor Prognosis Leukemia
Lead sponsor National Cancer Institute (NCI), NIH
Status Completed
Phase Phase 1
Study type Interventional
Conditions Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities, Adult Acute Myeloid Leukemia With Del(5q), 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 9 more
Intervention type Drug, Other
Interventions decitabine, vorinostat, laboratory biomarker analysis, pharmacological study
Enrollment 50
Start date Jun 1, 2006
Primary completion Oct 1, 2009
First posted Jul 27, 2006
Last update posted Jan 7, 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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