drugset / Trial / NCT00620321

A Study of LY2181308 Sodium in Patients With Relapsed or Refractory Acute Myeloid Leukemia

NCT00620321

Phase 2 Completed 24 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to understand the safety profile of LY2181308 sodium administered in combination with idarubicin and cytarabine to patients with relapsed or refractory acute myeloid leukemia (AML).

Timeline

Start
2008-03
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject GATAPARSEN Antisense oligonucleotide 750 mg Intravenous
Background Cytarabine Small molecule 1.5 g Intravenous
Background Idarubicin Small molecule 12 mg/m2 Intravenous