Etrasimod for the treatment of ulcerative colitis

Author:

Wils Pauline12ORCID,Peyrin-Biroulet Laurent34

Affiliation:

1. Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, University of Lille, F-59000 Lille, France

2. Department of Gastroenterology, Centre Hospitalier Régional Universitaire de Lille, University of Lille, 59000, France

3. University of Lorraine, CHRU-Nancy, Department of Gastroenterology, F-54000 Nancy, France

4. University of Lorraine, Inserm, NGERE, F-54000 Nancy, France

Abstract

Sphingosine-1-phosphate (S1P) and its receptor (S1PR) are involved in the pathogenesis of multiple immune-mediated inflammatory disorders, including inflammatory bowel disease. The use of S1PR modulators represents a new therapeutic option for ulcerative colitis patients. Etrasimod is an oral selective S1PR1, S1PR4 and S1PR5 modulator that inhibits the trafficking of lymphocytes from the lymph nodes into the blood. Recently, etrasimod has demonstrated efficacy in the phase II OASIS study and its open-label extension for the treatment of ulcerative colitis patients. This article reviews the mechanism of action of etrasimod and summarizes the available clinical efficacy and safety data regarding etrasimod, which is a promising drug in the treatment of patients with moderate to severe ulcerative colitis.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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