drugset / Trial / NCT00694356

Study of Dalotuzumab (MK-0646) in Adults With Solid Tumors (MK-0646-009)

NCT00694356

Phase 1 Completed 15 enrolled Merck Sharp & Dohme LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This clinical study evaluates the safety, tolerability, pharmacokinetics, and immunogenicity of dalotuzumab (MK-0646) in participants with relapsed or refractory locally advanced or metastatic solid tumors using once weekly and once every other week dose infusion regimens. The primary study hypothesis is that administration of dalotuzumab as a once weekly and an every other week infusion will be generally safe and well tolerated

Timeline

Start
2008-08-04
Primary completion
2009-03-18
Completion
2009-04-28

Drugs

EvaluationDrugModalityDoseRoute
Subject dalotuzumab Monoclonal antibody 5 mg/kg Intravenous
Subject dalotuzumab Monoclonal antibody 7.5 mg/kg Intravenous
Subject dalotuzumab Monoclonal antibody 10 mg/kg Intravenous

Indications