drugset / Trial / NCT00192465

Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI-524 in Healthy Adults

NCT00192465

Phase 1 Completed 30 enrolled MedImmune LLC
RandomizedParallel-groupOpen-labelPrevention

Summary

To provide safety, tolerability, pharmacokinetic, and immunogenicity data for MEDI-524 administered initially as a single dose to healthy adults in a dose escalation safety study before testing in the targeted pediatric population.

Timeline

Start
2003-11
Primary completion
2004-04
Completion
2004-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Motavizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Motavizumab Monoclonal antibody 15 mg/kg Intravenous
Subject Motavizumab Monoclonal antibody 30 mg/kg Intravenous