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Clinical Trial Summary

The purpose of this study is to assess safety, tolerability, pharmacokinetics and pharmacodynamics of MEDI-546 in Japanese SLE patients.


Clinical Trial Description

A phase 2, multicenter, open-label, dose-escalation study to evaluate the safety and tolerability of intravenous dose of MEDI-546, a human monoclonal antibody directed against type I interferon receptor (IFNAR), in Japanese subjects with active systemic lupus erythematosus (SLE) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01559090
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 2
Start date April 20, 2012
Completion date February 21, 2017

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