drugset / Trial / NCT01119456

A Study of IMC-RON8 in Advanced Solid Tumors

NCT01119456 ↗

Phase 1 Completed 39 enrolled Eli Lilly and Company
SequentialOpen-labelTreatment

Summary

A dose escalation study to determine the maximum tolerated dose of IMC-RON8 in participants with solid tumors. Participants can either be dosed once a week, or once every other week.

Timeline

Start
2010-05
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject NARNATUMAB Monoclonal antibody 5 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 10 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 15 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 20 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 25 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 30 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 35 mg/kg Intravenous
Subject NARNATUMAB Monoclonal antibody 40 mg/kg Intravenous

Indications