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Clinical Trial Summary

This study will be conducted to characterize pharmacokinetics, pharmacodynamics, safety, and tolerability of anifrolumab given via the subcutaneous (SC) route of administration in adult Systemic Lupus Erythematosus (SLE) subjects with a type I Interferon (IFN) test high result and active skin manifestations while receiving Standard of Care (SOC) treatment. In addition, the efficacy of anifrolumab on SLE skin manifestations will be characterized.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02962960
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 2
Start date February 14, 2017
Completion date December 17, 2018

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