drugset / Trial / NCT02182063

A Study With BIBF 1120 in Patients With Hormone Refractory Prostate Cancer

NCT02182063

Phase 2 Completed 81 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

The aim of this study was to evaluate the efficacy of two different doses of BIBF 1120 (250 mg twice daily versus 150 mg twice daily) in an exploratory manner. Safety, quality of life and pharmacokinetic parameters on a sub-sample of 20 patients were also analysed for the two different doses.

Timeline

Start
2005-11
Primary completion
2007-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Nintedanib Small molecule 150 mg Oral
Subject Nintedanib Small molecule 250 mg Oral

Indications