drugset / Trial / NCT01524224

A Dose-Escalation Study in Participants With Advanced Cancer

NCT01524224

Phase 1 Completed 29 enrolled Eli Lilly and Company
SequentialOpen-labelTreatment

Summary

This study is a multicenter, open-label, dose-escalation phase 1 study of intravenous (IV) LY2495655 in participants with advanced cancer.

Timeline

Start
2008-01
Primary completion
2012-11
Completion
2016-01

Drugs

EvaluationDrugModalityDoseRoute
Subject LANDOGROZUMAB Monoclonal antibody 2 mg Intravenous
Subject LANDOGROZUMAB Monoclonal antibody 7 mg Intravenous
Subject LANDOGROZUMAB Monoclonal antibody 21 mg Intravenous
Subject LANDOGROZUMAB Monoclonal antibody 70 mg Intravenous
Subject LANDOGROZUMAB Monoclonal antibody 210 mg Intravenous
Subject LANDOGROZUMAB Monoclonal antibody 700 mg Intravenous

Indications

No indication recorded.