A Treatment Effectiveness Study Among SLE Patients Receiving Anifrolumab in Routine Clinical Practice
← catalyst calendarNCT05637112 · readout in 1,594 d
Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Parexel.
Phase
—
Status
Active, not recruiting
Study type
Observational
Enrollment
551actual
Sites
79
Countries
Austria, Belgium, Canada +6
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2023-02-27 | actual | When the study began enrolling |
| Primary completion | 2030-12-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2030-12-30 | estimated | The whole study's end, after follow-up |
| First posted | 2022-12-05 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-26 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Systemic Lupus Erythematosus
Intervention
- Other: None (Observational study) — also filed as Observational Study
Primary outcomes
what the primary-completion date above is the date OFDisease activity assessed by the Physician Global Assessment (PGA)
measured From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Disease activity assessed by Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K)
measured From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Proportion of patients attaining the composite endpoint of lupus low disease activity (LLDAS)
measured From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Publications
- PMID 39578022 — linked by the registry
Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.
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