drugset / Trial / NCT00701766

BI 2536 Infusional Treatment in Patients Over 60 Years of Age With Refractory or Relapsed Acute Myeloid Leukaemia

NCT00701766

Phase 2 Completed 71 enrolled Boehringer Ingelheim
Parallel-groupTreatment

Summary

The present trial will be performed to determine the MTD and to evaluate the efficacy of BI 2536 in the treatment of elderly patients with relapsed or refractory AML. Different schedules will be compared to identify the better dosing schedule for the further development programme of BI 2536. Dose escalation starting with the maximum tolerated dose previously determined in patients with advanced solid cancers will be performed to determine the maximum tolerated dose for AML patients.

Timeline

Start
2006-10
Primary completion
2009-10
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 2536 Small molecule Intravenous