drugset / Trial / NCT02689505

Weekly BI 836880 in Patients With Advanced Solid Tumors

NCT02689505

Phase 1 Completed 24 enrolled Boehringer Ingelheim
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase I, multi-centre, non-randomized, uncontrolled, open-label, dose escalating study of BI 836880 administered intravenously once a week. The eligible patient population will be patients with advanced solid tumors. The primary objective of this trial is to determine the maximum tolerated dose (MTD) and recommended Phase II doses for BI 836880 in patients with solid tumors. Preliminary safety data will be evaluated as secondary objectives. Subsequently, pharmacokinetic profile, pharmacodynamic changes in circulating biomarkers and Dynamic Contrast-Enhanced Magnetic Resonance Imaging ( DCE-MRI), anti-tumor activity and the immunogenicity of BI 836880 will be explored up to a total of 40 patients with advanced solid tumors. Dose escalation will be guided by a Bayesian logistic regression model with over dose control (EWOC) using at least 2 patients per dose cohorts. Safety criteria will be followed, including adverse events according to Common Terminology Criteria (CTCAE version 4.03), incidence of dose limiting toxicities, physical examination, vital signs, safety laboratory parameters and Eastern Cooperative Oncology Group (ECOG).

Timeline

Start
2016-04-04
Primary completion
2019-07-31
Completion
2019-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 836880 Protein / enzyme biologic 40 mg Intravenous
Subject BI 836880 Protein / enzyme biologic 120 mg Intravenous
Subject BI 836880 Protein / enzyme biologic 150 mg Intravenous
Subject BI 836880 Protein / enzyme biologic 180 mg Intravenous
Subject BI 836880 Protein / enzyme biologic 240 mg Intravenous

Indications