RecruitingNCT07424261

NIS to Examine Disease Activity in SLE Patients Treated With Subcutaneous Anifrolumab in Routine Care

Effectiveness of Subcutaneous Anifrolumab in Systemic Lupus Erythematodes - A Non-interventional, Prospective, Multicenter Study on Disease Activity in SLE Patients Treated With Subcutaneous Anifrolumab in Routine Care


Sponsor

AstraZeneca

Enrollment

125 participants

Start Date

Mar 19, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

VIOLET is a prospective, single-arm, multi-centre, non-interventional study (NIS) evaluating real-world clinical and patient-reported outcome (PRO) data in adult patients who are initiated on subcutaneous anifrolumab treatment of systemic lupus erythematosus (SLE) in line with the applicable european summary of product characteristics (SmPC) and neither having used anifrolumab subcutaneous (SC) or intravenous (IV) before.


Eligibility

Min Age: 18 YearsMax Age: 130 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with lupus erythematosus, systemic. The study is currently recruiting participants at 16 locations. People eligible for this study include aged 18 Years to 130 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(16)

Research Site

Altenburg, Germany

Research Site

Bad Bramstedt, Germany

Research Site

Berlin, Germany

Research Site

Chemnitz, Germany

Research Site

Erlangen, Germany

Research Site

Heidelberg, Germany

Research Site

Herne, Germany

Research Site

Kassel, Germany

Research Site

Leipzig, Germany

Research Site

Meerbusch-Lank, Germany

Research Site

München, Germany

Research Site

Planegg, Germany

Research Site

Schwerin, Germany

Research Site

Trier, Germany

Research Site

Wetzlar, Germany

Research Site

Wuppertal, Germany

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NCT07424261


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