drugset / Trial / NCT00930683

A Study to Evaluate Safety and Tolerability of Multiple Doses of MEDI-546 in Adult Subjects With Scleroderma

NCT00930683

Phase 1 Completed 34 enrolled MedImmune LLC
RandomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and tolerability of a multiple-dosed drug (MEDI-546) in adults with scleroderma.

Timeline

Start
2009-09
Primary completion
2010-05
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 1 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 3 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 5 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 10 mg/kg Intravenous
Subject Anifrolumab Monoclonal antibody 20 mg/kg Intravenous

Indications