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Abstract Number: 1544

Voclosporin in Lupus Nephritis: Meta-Analysis of 6-Month and 1-Year Efficacy with 1-Year Safety Outcomes

Sri Laxmi Priya Sunkara1, Ravi Medarametla2, Megha Kotha3 and Wael Jarjour4, 1White river medical center, batesville, AR, 2Mamata Medical College, Guntur, Andhra Pradesh, India, 3Ohio State University, Columbus, OH, 4The Ohio State University, Columbus, OH

Meeting: ACR Convergence 2025

Keywords: autoimmune diseases, Lupus nephritis, Nephritis, Renal

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Session Information

Date: Monday, October 27, 2025

Title: (1517–1552) Systemic Lupus Erythematosus – Treatment Poster II

Session Type: Poster Session B

Session Time: 10:30AM-12:30PM

Background/Purpose: Lupus nephritis (LN), is the most sever organ manifestation of systemic lupus erythematosus (SLE) and it contributes significantly to morbidity and mortality. . Standard therapies—high-dose corticosteroids combined with mycophenolate mofetil or cyclophosphamide—achieve complete renal remission in a limited subset of patients and carry substantial toxicity. Calcineurin inhibitors (CNIs) target immune dysregulation and podocyte injury. Voclosporin, a novel CNI, inhibits T-cell activation and reduces proteinuria, offering potential therapeutic benefit in LN.

Methods: A systematic search of PubMed, Embase, and Cochrane databases was conducted for English-language studies evaluating voclosporin in LN and reporting relevant efficacy or safety outcomes. Two randomized controlled trials met inclusion criteria. Data were pooled using inverse variance weighting with a random-effects model in R Studio. Forest plots were used to illustrate pooled effect estimates, and heterogeneity was assessed.

Results: A total of 533 patients from two studies were included. Voclosporin significantly increased complete renal response (CRR) at 6 months (RR 1.67; 95% CI: 1.24–2.25; p=0.0008) and 1 year (RR 1.91; 95% CI: 1.48–2.48; p< 0.0001) compared to placebo. Rates of overall adverse events (RR 1.04; 95% CI: 0.98–1.10; p=0.16), serious adverse events (RR 1.26; 95% CI: 0.71–2.25; p=0.43), and infections (RR 1.15; 95% CI: 0.98–1.36; p=0.096) were similar between groups. However, voclosporin was associated with significantly higher gastrointestinal (RR 1.37; 95% CI: 1.06–1.76; p=0.016) and neurological adverse events (RR 1.79; 95% CI: 1.18–2.72; p=0.006) at 1 year.

Conclusion: Voclosporin significantly improves CRR at 6 months and 1 year in patients with LN, with an overall safety profile comparable to placebo. However, gastrointestinal and neurological adverse events were more common. Further studies are needed to assess long-term outcomes, define steroid-sparing protocols, optimize dosing, and evaluate efficacy across diverse populations to determine voclosporin’s definitive role in LN treatment.

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Disclosures: S. Sunkara: None; R. Medarametla: None; M. Kotha: None; W. Jarjour: None.

To cite this abstract in AMA style:

Sunkara S, Medarametla R, Kotha M, Jarjour W. Voclosporin in Lupus Nephritis: Meta-Analysis of 6-Month and 1-Year Efficacy with 1-Year Safety Outcomes [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/voclosporin-in-lupus-nephritis-meta-analysis-of-6-month-and-1-year-efficacy-with-1-year-safety-outcomes/. Accessed .
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