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Active, not recruiting Observational

Anifrolumab Real-world Treatment Outcomes in Systemic Lupus Erythematosus

NCT06673043 · tracked via the Priya Life Science Poland tracker
Phase
Observational
Started
2025-02-28
Last updated
2026-09-18

Condition(s) studied

Lupus Erythematosus, Systemic

Investigational drug(s) / intervention(s)

Anifrolumab →

Anifrolumab: Anifrolumab 300 mg concentrate for solution for infusion

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult (aged ≥18 years old) patients with SLE who received anifrolumab treatment in the frames of NDP in Poland. 2. Patients willing to participate in the study and signed Informed Consent Form (ICF). Exclusion Criteria: 1. 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. 2. Cognitive incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

Primary outcome measure(s)

  • Change from index date in Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) score — at month 12

Trial sites (11)

FacilityCityRegionStatus
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
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06673043 on ClinicalTrials.gov ↗ ← All trials in Poland