drugset / Trial / NCT00578682

A Phase I, Randomized, Double-Blind, Single-Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI-557

NCT00578682 ↗

Phase 1 Completed 31 enrolled MedImmune LLC
RandomizedSingle-groupDouble-blindTreatment

Summary

To evaluate the safety and tolerability of a single IV dose of MEDI-557.

Timeline

Start
2007-12
Primary completion
2010-10
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI-557 Monoclonal antibody 0.3 mg/kg Intravenous
Subject MEDI-557 Monoclonal antibody 3 mg/kg Intravenous
Subject MEDI-557 Monoclonal antibody 15 mg/kg Intravenous
Subject MEDI-557 Monoclonal antibody 30 mg/kg Intravenous

Indications

No indication recorded.