drugset / Trial / NCT01403974

Phase I Trial of BI 836845 for Various Solid Cancer

NCT01403974

Phase 1 Completed 61 enrolled Boehringer Ingelheim
RandomizedSequentialOpen-labelTreatment

Summary

This study is a phase I, open-label, dose escalation trial to determine the maximum tolerated dose (MTD) or the relevant biological dose (RBD) in the absence if a MTD of a new drug BI 836845 which blocks the insulin-like growth factor (IGF) pathway believed to be involved in cancer growth. BI 836845 will be administered for the very first time into cancer patients. The study will also look at the overall safety of the drug, and examine the drug levels in the body at specific timepoints during the trial (pharmacokinetic profile); the effect the drug may have on tumours will also be examined (pharmacodynamics).

Timeline

Start
2011-07-19
Primary completion
2015-07-08
Completion
2015-12-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Xentuzumab Monoclonal antibody 10 mg Intravenous
Subject Xentuzumab Monoclonal antibody 20 mg Intravenous
Subject Xentuzumab Monoclonal antibody 40 mg Intravenous
Subject Xentuzumab Monoclonal antibody 60 mg Intravenous
Subject Xentuzumab Monoclonal antibody 90 mg Intravenous
Subject Xentuzumab Monoclonal antibody 135 mg Intravenous
Subject Xentuzumab Monoclonal antibody 200 mg Intravenous
Subject Xentuzumab Monoclonal antibody 300 mg Intravenous
Subject Xentuzumab Monoclonal antibody 450 mg Intravenous
Subject Xentuzumab Monoclonal antibody 600 mg Intravenous
Subject Xentuzumab Monoclonal antibody 800 mg Intravenous
Subject Xentuzumab Monoclonal antibody 1000 mg Intravenous
Subject Xentuzumab Monoclonal antibody 1050 mg Intravenous
Subject Xentuzumab Monoclonal antibody 1400 mg Intravenous
Subject Xentuzumab Monoclonal antibody 1800 mg Intravenous

Indications