drugset / Trial / NCT00946699

A Study of the Safety and Tolerability of MEDI-551 in Scleroderma

NCT00946699

Phase 1 Completed 50 enrolled MedImmune LLC
RandomizedSingle-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of intravenously administered MEDI-551 over escalating single doses in adult subjects with Scleroderma

Timeline

Start
2010-03
Primary completion
2012-03
Completion
2014-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Inebilizumab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Inebilizumab Monoclonal antibody 1 mg/kg Intravenous
Subject Inebilizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Inebilizumab Monoclonal antibody 10 mg/kg Intravenous

Indications