Clinical trial

Daunorubicin Hydrochloride, Cytarabine and Oblimersen Sodium in Treating…

NCT00085124 · National Cancer Institute (NCI), NIH · Completed

Key facts

NCT number NCT00085124
Title Daunorubicin Hydrochloride, Cytarabine and Oblimersen Sodium in Treating Patients With Previously Untreated Acute Myeloid Leukemia
Official title A Phase III Study of Daunorubicin and Cytarabine +/- G3139 (Genasense, Oblimersen Sodium, NSC #683428, IND #58842), a BCL2 Antisense Oligodeoxynucleotide, in Previously Untreated Patients With Acute Myeloid Leukemia (AML) > / = 60 Years
Lead sponsor National Cancer Institute (NCI), NIH
Status Completed
Phase Phase 3
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 2 more
Intervention type Biological, Drug, Other
Interventions oblimersen sodium, cytarabine, daunorubicin hydrochloride, laboratory biomarker analysis
Enrollment 500
Start date Dec 1, 2003
Primary completion Jun 1, 2007
First posted Jun 11, 2004
Last update posted May 30, 2024
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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