drugset / Trial / NCT02182206

An Dose Escalation Study of Treatment With BIBF 1120 in Patients With Advanced Solid Tumours

NCT02182206

Phase 1 Completed 50 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

Maximum Tolerated Dose (MTD), safety, pharmacokinetics, efficacy of BIBF 1120, pharmacodynamic parameters (Dynamic Contrast-Enhanced Magnetic Resonance Imaging (DCE-MRI))

Timeline

Start
2003-06
Primary completion
2005-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Nintedanib Small molecule 100 mg Oral
Subject Nintedanib Small molecule 250 mg Oral
Subject Nintedanib Small molecule 450 mg Oral

Indications