RecruitingNCT06673043

Anifrolumab Real-world Treatment Outcomes in Systemic Lupus Erythematosus

Anifrolumab Real-world Treatment Outcomes in Polish Patients With Systemic Lupus Erythematosus (SLE). Multicenter, Non-interventional Study


Sponsor

AstraZeneca

Enrollment

100 participants

Start Date

Feb 28, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The Polish multicentre observational (non-interventional) study aiming to collect data on the characteristic of patients with systemic lupus erythematosus and clinical outcomes of anifrolumab administered in the scope of routine clinical practice.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Adult (aged ≥18 years old) patients with SLE who received anifrolumab treatment in the frames of NDP in Poland.
  • Patients willing to participate in the study and signed Informed Consent Form (ICF).

Exclusion Criteria2

  • Those who participated in anifrolumab clinical trial in the past, and/or those who participated/plans to participate in clinical trial on/after the date of first anifrolumab infusion through NDP.
  • Cognitive incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

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Interventions

DRUGAnifrolumab

Anifrolumab 300 mg concentrate for solution for infusion


Locations(11)

Research Site

Bydgoszcz, Poland

Research Site

Bytom, Poland

Research Site

Gdansk, Poland

Research Site

Katowice, Poland

Research Site

Krakow, Poland

Research Site

Lodz, Poland

Research Site

Lublin, Poland

Research Site

Poznan, Poland

Research Site

Rzeszów, Poland

Research Site

Warsaw, Poland

Research Site

Wroclaw, Poland

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NCT06673043


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