drugset / Trial / NCT00730821

Phase I of BIBW 2992/BIBF 1120 Combination Therapy in Solid Tumors

NCT00730821

Phase 1 Completed 28 enrolled Boehringer Ingelheim
Treatment

Summary

The primary objective of this trial is to determine the MTD of the combination of BIBW 2992/BIBF 1120 therapy administered concomitantly in a 28-day cycle schedule. Secondary objectives are the collection of antitumor efficacy data, the determination of pharmacokinetic parameters of BIBF 1120 and BIBW 2992, and if data allow the determination of the pharmacokinetic influence of BIBW 2992 on BIBF 1120 and vice versa.

Timeline

Start
2007-01
Primary completion
2009-08
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule
Subject Nintedanib Small molecule

Indications