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Clinical Trial Summary

The purpose of this study is to characterise long-term safety and tolerability of intravenous anifrolumab.


Clinical Trial Description

This is a Phase 3, multicentre, multinational, randomised, double-blind, placebo-controlled extension study to characterising the long term safety and tolerability of of an intravenous treatment regimen of anifrolumab versus placebo in subjects with moderately to severely active systemic lupus erythematosus who completed a Phase 3 study (D3461C00004 or D3461C00005) through the 52-week double-blind treatment period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02794285
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 3
Start date June 30, 2016
Completion date December 21, 2021

See also
  Status Clinical Trial Phase
Active, not recruiting NCT04931563 - Anifrolumab Asian PhIII Efficacy Study for Systemic Lupus Erythematosus (SLE) Phase 3
Terminated NCT04680637 - Efficacy and Safety of Efavaleukin Alfa in Subjects With Active Systemic Lupus Erythematosus Phase 2
Completed NCT02446912 - Efficacy and Safety of Two Doses of Anifrolumab Compared to Placebo in Adult Subjects With Active Systemic Lupus Erythematosus Phase 3
Completed NCT02446899 - Efficacy and Safety of Anifrolumab Compared to Placebo in Adult Subjects With Active Systemic Lupus Erythematosus Phase 3