drugset / Trial / NCT00904839

BIBF 1120 Versus Bevacizumab in Metastatic Colorectal Cancer

NCT00904839 ↗

Phase 2 Completed 128 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate PFS rate at 9 months of BIBF 1120 in combination with mFolfox6 compared with mFolfox6 combined to bevacizumab in first line patients with metastatic colorectal cancer.

Timeline

Start
2009-05
Primary completion
2012-01
Completion
2012-01

Outcome

Missed primary endpoint

registry Difference -8.1 (95% CI -27.8 to 11.5); Kaplan-Meier NCT00904839 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject 100 mg/Kg solution , IV infusion Unknown 100 mg/kg Intravenous
Comparator Nintedanib Small molecule 100 mg —
Comparator Nintedanib Small molecule 150 mg —

Indications