drugset / Trial / NCT02171663

Dose Escalation Study of BIBW 2992 in Patients With Advanced Solid Tumors

NCT02171663

Phase 1 Completed 43 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

The primary objective was the assessment of safety of BIBW 2992 as assessed by the maximum tolerated dose (MTD). Secondary objectives were collection of overall safety data, antitumor efficacy data, as well as the determination of pharmacokinetics and the pharmacodynamic modulation of biomarkers by BIBW 2992.

Timeline

Start
2004-03
Primary completion
2006-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Afatinib Small molecule Oral

Indications