drugset / Trial / NCT00299819

Safety and Tolerability of MEDI-545 in Patients Who Have Systemic Lupus Erythematosus (SLE)

NCT00299819 ↗

Phase 1 Completed 45 enrolled MedImmune LLC
RandomizedSingle-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of intravenously administered MEDI-545 compared with placebo, over a dose escalation range of 0.3-30 mg/kg, in adult patients with SLE and who are receiving 20 mg/day or less of prednisone orally or an equivalent dose of another oral corticosteroid.

Timeline

Start
2006-03
Primary completion
—
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Sifalimumab Monoclonal antibody 0.3 mg/kg Intravenous
Comparator Sifalimumab Monoclonal antibody 1 mg/kg Intravenous
Comparator Sifalimumab Monoclonal antibody 3 mg/kg Intravenous
Comparator Sifalimumab Monoclonal antibody 10 mg/kg Intravenous
Comparator Sifalimumab Monoclonal antibody 30 mg/kg Intravenous