drugset / Trial / NCT00998296

Phase I Dose Escalation Study of Concomitant BIBF 1120 and BIBW 2992 in Patients With Advanced Solid Tumours.

NCT00998296

Phase 1 Completed 70 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this trial is to determine the Maximum Tolerated Dose (MTD) of the combination of BIBW 2992/BIBF 1120 therapy administered concomitantly. The MTD will provide dosing recommendation for subsequent phase II trials in patients with metastatic cancer.

Timeline

Start
2009-10
Primary completion
2012-12
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule 10 mg
Subject Afatinib Small molecule 20 mg
Subject Afatinib Small molecule 30 mg
Subject Afatinib Small molecule 40 mg
Subject Nintedanib Small molecule 150 mg
Subject Nintedanib Small molecule 200 mg

Indications