drugset / Trial / NCT00785538

A Study of IMC-A12 in Participants With Tumors Who No Longer Respond to Treatment or For Whom No Treatment is Available

NCT00785538

Phase 1 Completed 24 enrolled Eli Lilly and Company
SequentialOpen-labelTreatment

Summary

The purpose of this study is to determine if IMC-A12 is safe for participants, and also to determine the best dose of IMC-A12 to give to participants.

Timeline

Start
2005-10
Primary completion
2011-01
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cixutumumab Monoclonal antibody 3 mg/kg Intravenous
Subject Cixutumumab Monoclonal antibody 6 mg/kg Intravenous
Subject Cixutumumab Monoclonal antibody 10 mg/kg Intravenous
Subject Cixutumumab Monoclonal antibody 15 mg/kg Intravenous
Subject Cixutumumab Monoclonal antibody 21 mg/kg Intravenous
Subject Cixutumumab Monoclonal antibody 27 mg/kg Intravenous

Indications