drugset / Trial / NCT00373373

Efficacy of Sorafenib Added to Standard Primary Therapy in Elderly Patients With Newly Diagnosed AML

NCT00373373

Phase 2 Completed 200 enrolled University Hospital Muenster Bayer · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of the study is to determine, whether the addition of Sorafenib to standard chemotherapy in elderly patients with newly diagnosed AML improves treatment results (event free survival).

Timeline

Start
2006-09
Primary completion
2009-07
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Sorafenib Small molecule 400 mg