drugset / Trial / NCT02171702

Dose Escalation Study of Oral Treatment With BIBW 2992 in Patients With Advanced Solid Tumours

NCT02171702

Phase 1 Completed 53 enrolled Boehringer Ingelheim
RandomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of the study was to identify the maximum tolerated dose and to evaluate safety, pharmacokinetics, pharmacodynamic parameters, and efficacy of BIBW 2992.

Timeline

Start
2004-11
Primary completion
2007-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule Oral

Indications