Therapeutic Potential of Etrasimod in the Management of Moderately-to-Severely Active Ulcerative Colitis: Evidence to Date

被引:3
|
作者
Glassner, Kerri [1 ,2 ,3 ]
Fan, Christopher [1 ]
Irani, Malcolm [1 ]
Abraham, Bincy P. [1 ,2 ,3 ]
机构
[1] Houston Methodist Gastroenterol Associates, Houston Methodist, Houston, TX USA
[2] Cornell Univ, Weill Cornell Med Coll, New York, NY USA
[3] Houston Methodist Acad Inst, Houston Methodist, Houston, TX USA
关键词
etrasimod; inflammation; ulcerative colitis; small molecule; sphingosine 1 phosphate modulator; MAINTENANCE THERAPY; INDUCTION; SPHINGOSINE-1-PHOSPHATE; MODULATION; OZANIMOD;
D O I
10.2147/CEG.S391706
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Etrasimod is a sphingosine 1 phosphate (S1P) receptor modulator approved for the treatment of moderate to severely active ulcerative colitis (UC). Etrasimod selectively activates S1P1,4,5 receptors with no detectable activity on S1P2,3. The ELEVATE clinical trials evaluated the efficacy and safety of etrasimod for UC. Etrasimod showed clinically significant improvement in clinical remission at weeks 12 and 52 compared to placebo. Etrasimod showed greater efficacy in patients who were biologic naive. Etrasimod was also effective in a subgroup of patients with isolated proctitis. The medication should be avoided in pregnancy and lactation, certain cardiac conditions including brady-arrythmias, and those with a history of skin cancer. Etrasimod has a shorter half-life and fewer drug-drug and food interactions as compared to the S1P receptor modulator ozanimod. In addition, no dosing titration is required. Etrasimod is a promising treatment option for UC patients with moderate to severe inflammation, particularly those who have no prior biologic exposure, are not considering pregnancy, and prefer oral therapy.
引用
收藏
页码:337 / 345
页数:9
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