P138 Preclinical and clinical characterization of cenerimod, a potent, selective, and orally active sphingosine-1-phosphate receptor 1 modulator in SLE. (23rd March 2020)

• Record Type: Journal Article
• Authors: Strasser, Daniel S; Gerossier, Estelle; Sippel, Virginie; Grieder, Ursula; Kieninger-Graefitsch, Andrea; Pierlot, Gabin; Farine, Hervé; Kulig, Paulina; Keller, Marcel; Froidevaux, Sylvie; Trendelenburg, Marten; Murphy, Mark; Martinic, Marianne
• Is Part Of: Lupus science & medicine. Volume 7(2020)Supplement 1
• Page Start: A97
• Page End: A97
• Publication Date: 2020-03-23
• Subjects: Systemic lupus erythematosus -- Periodicals; 616.772005
• DOI: 10.1136/lupus-2020-eurolupus.182
• Languages: English
• ISSNs: 2398-8851

Abstract

Abstract : Background: Reported here is the characterization of cenerimod, a novel, potent, selective, and orally active sphingosine-1-phosphate receptor 1 (S1P1 ) modulator in the context of SLE. Methods: Lymphocytes from patients with SLE and healthy subjects were assessed for cenerimod-induced S1P1 receptor internalization. Efficacy of cenerimod was evaluated in the MRL/lpr lupus mouse model. In a 12-week phase 2 clinical trial in SLE subjects treated with multiple doses of cenerimod (NCT02472795 ), lymphocyte subsets and inflammatory biomarkers were characterized. Results: Cenerimod was potent and efficacious at inducing S1P1 receptor internalization in T and B lymphocytes with an EC50 of ∼15 nM in both healthy subjects and patients with SLE. In lupus-like MRL/lpr mice treated with cenerimod, circulating T and B lymphocytes were reduced, which resulted in reduced immune infiltrates into tissue, reduced autoantibody production and inflammation, preserved organ function, and increased survival. In SLE subjects treated with cenerimod for 12 weeks, a dose-dependent reduction of circulating T cells (95%), B cells (90%), and antibody-secreting cells (85%) was evident. Furthermore, a reduction in anti-dsDNA antibodies and IFN-α, two key inflammatory molecules, was observed. Conclusion: Cenerimod was potent and efficacious in reducing S1P1 receptor surface expression on lymphocytes, resulting in reduced circulating T and B lymphocyte populations, including antibody-secreting cells, and a decrease in inflammatory biomarkers in SLE subjects. Furthermore, cenerimod significantly ameliorated systemic and organ-specific autoimmunity in a mouse model of SLE. These results warranted the further investigation of the clinical efficacy and safety of cenerimod in the ongoing phase 2b clinical trial (NCT03742037 ). Acknowledgments: This research was funded by Idorsia Pharmaceuticals Ltd.