Finding studies
Finding studies
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Lead
MedImmune LLC
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 who have SLE and who are receiving 20 mg/day or less of prednisone orally or an equivalent dose of another oral corticosteroid. The secondary objective of this study is to describe the pharmacokinetics and potential immunogenicity of MEDI-545.
Age
18–80
Sex
ALL
Healthy volunteers
Not accepted
