Update on biologics in SLE

PURPOSE OF REVIEW: Until recently, biologic treatment options for systemic lupus erythematosus (SLE) remained limited. Recent studies have substantially expanded the therapeutic landscape. We summarize where the field currently stands and which developments are likely to shape practice next. RECENT FINDINGS: Obinutuzumab, a type II anti-CD20 antibody, improved complete renal response in REGENCY, was approved for lupus nephritis in the United States and European Union, and was incorporated into the 2025 EULAR recommendations; in nonrenal SLE, ALLEGORY met its primary and all key secondary endpoints. A weekly subcutaneous formulation of the type I interferon receptor antagonist anifrolumab was approved after TULIP-SC. The dual BLyS/APRIL inhibitor telitacicept was effective in a Chinese phase 3 trial, and the CD40 ligand inhibitor dapirolizumab pegol met its primary endpoint in PHOENYCS GO. Ianalumab, litifilimab, and nipocalimab are advancing through phase 3 development. SUMMARY: SLE now has an expanding late-stage therapeutic pipeline. The principal challenges are now patient selection, sequencing and combination of agents, long-term safety and access.

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Publication Details

Journal
Current Opinion in Rheumatology
Published
2026-11-06
DOI
https://doi.org/10.1097/bor.0000000000001214
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Update on biologics in SLE

Vasileios C. Kyttaris, Milena Delai
Current Opinion in Rheumatology
Systemic Lupus Erythematosus Research
article

Update on biologics in SLE

Vasileios C. Kyttaris, Milena Delai
article en

Abstract

PURPOSE OF REVIEW: Until recently, biologic treatment options for systemic lupus erythematosus (SLE) remained limited. Recent studies have substantially expanded the therapeutic landscape. We summarize where the field currently stands and which developments are likely to shape practice next. RECENT FINDINGS: Obinutuzumab, a type II anti-CD20 antibody, improved complete renal response in REGENCY, was approved for lupus nephritis in the United States and European Union, and was incorporated into the 2025 EULAR recommendations; in nonrenal SLE, ALLEGORY met its primary and all key secondary endpoints. A weekly subcutaneous formulation of the type I interferon receptor antagonist anifrolumab was approved after TULIP-SC. The dual BLyS/APRIL inhibitor telitacicept was effective in a Chinese phase 3 trial, and the CD40 ligand inhibitor dapirolizumab pegol met its primary endpoint in PHOENYCS GO. Ianalumab, litifilimab, and nipocalimab are advancing through phase 3 development. SUMMARY: SLE now has an expanding late-stage therapeutic pipeline. The principal challenges are now patient selection, sequencing and combination of agents, long-term safety and access.

Current Opinion in Rheumatology
Beth Israel Deaconess Medical Center (US), Harvard University (US)
Good health and well-being
Openalex Percentile: Top 14%
Systemic Lupus Erythematosus Research
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