drugset / Trial / NCT00893373

Study Evaluating Sorafenib Added to Standard Primary Therapy in Patients With Newly Diagnosed Acute Myeloid Leukemia Less Than 60 Years of Age

NCT00893373 ↗

Phase 2 Completed 276 enrolled Technical University Dresden Bayer · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Sorafenib is a multikinase inhibitor which is acting on various cellular pathways involved in the genesis of acute myeloid leukemia (AML). Sorafenib is therefore a promising candidate for improvement of chemotherapy results in AML. This clinical trial evaluates the efficacy of sorafenib added to standard chemotherapy for AML in patients between 18 and 60 years of age. Patients are randomised to receive either sorafenib capsules or placebo in addition to their chemotherapy. The placebo and the sorafenib group will be compared regarding event-free survival and other clinical outcomes. An event is either treatment failure or relapse or death. According to the study hypothesis, the sorafenib group will have less events than the placebo group.

Timeline

Start
2009-03
Primary completion
2011-11
Completion
2014-09

Outcome

Met primary endpoint

paper hazard ratio [HR] 0·64, 95% CI; 0·45-0·91; p=0·013). PMID 26549589 ↗

paper median event-free survival was 9 months (95% CI 4-15) in the placebo group versus 21 months (9-32) in the sorafenib group PMID 26549589 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 400 mg —