drugset / Trial / NCT01137006

An Open-Label, Dose-Escalation Study of IMC-20D7S In Participants With Malignant Melanoma

NCT01137006 ↗

Phase 1 Completed 27 enrolled Eli Lilly and Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

A dose-escalation study designed to determine the safety, maximum tolerated dose (MTD), anti-melanoma activity, antibody blood levels and progression-free survival (PFS) in participants with malignant melanoma receiving IMC-20D7S either every 2 weeks or every 3 weeks.

Timeline

Start
2010-06
Primary completion
2012-08
Completion
2012-08

Drugs

EvaluationDrugModalityDoseRoute
Subject FLANVOTUMAB Monoclonal antibody 5 mg/kg Intravenous
Subject FLANVOTUMAB Monoclonal antibody 10 mg/kg Intravenous
Subject FLANVOTUMAB Monoclonal antibody 20 mg/kg Intravenous
Subject FLANVOTUMAB Monoclonal antibody 30 mg/kg Intravenous

Indications