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