Current perspectives on FTY720

被引:22
作者
Martini, Sebastian
Peters, Harm
Boehler, Torsten
Budde, Klemens
机构
[1] Univ Med Berlin, Charite, Dept Nephrol, D-10117 Berlin, Germany
[2] CHU Rangueil, INSERM, Inst Louis Bugnard, U466, F-31054 Toulouse, France
关键词
fingolimod; FTY; FTY720; multiple sclerosis; renal transplantation; sphingosine-1-phosphate;
D O I
10.1517/13543784.16.4.505
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The search for effective immunosuppressants with fewer side effects continues not only for transplantation, but also for autoimmune diseases. With a novel mechanism of action (sphingosine-1 receptor modulation), oral FTY720 (fingolimod) has the potential to address this need. FTY720 has been preclinically tested with promising results in transplantation and autoimmune disease models. Phase I studies explored the pharmacokinetics and pharmacodynamics of this novel therapeutic concept. Recently, the surprising results of two sister Phase III studies in de novo renal transplant patients, as well as a Phase II study in patients with relapsing multiple sclerosis, were published. This review discusses these findings as well as their implications for the future of sphingosine-1 receptor modulation.
引用
收藏
页码:505 / 518
页数:14
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