Anifrolumab Real-world Treatment Outcomes in Systemic Lupus Erythematosus
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| 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 |
On this site
📄 Saphnelo (anifrolumab) drug profile →More AstraZeneca trials in Poland
Other trials for the same condition
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