芬戈莫德
1-磷酸鞘氨醇
医学
药理学
鞘氨醇
类风湿性关节炎
药品
鞘氨醇激酶
鞘氨醇激酶1
单克隆抗体
临床试验
血管生成
药物开发
多发性硬化
免疫学
受体
癌症研究
内科学
抗体
作者
Dagmar Meyer zu Heringdorf,Katja Ihlefeld,Josef Pfeilschifter
出处
期刊:Handbook of experimental pharmacology
日期:2013-01-01
卷期号:: 239-253
被引量:16
标识
DOI:10.1007/978-3-7091-1368-4_13
摘要
The recent success of FTY720 (Fingolimod, Gilenya®), which has been approved for the treatment of relapsing–remitting multiple sclerosis and is the first-in-class sphingosine-1-phosphate (S1P) receptor modulating drug, has boosted the interest in further drug development in this area. Several selective S1P1 receptor-modulating drugs are being investigated in clinical trials for the treatment of diverse autoimmune disorders. Sphingosine kinase inhibitors are under development for the treatment of cancer, aberrant angiogenesis and inflammatory diseases; an inhibitor of SK2 with relatively low affinity is being analysed in patients with advanced solid tumours. While an indirect S1P lyase inhibitor has just failed the proof of concept in patients with rheumatoid arthritis, S1P lyase is still a promising target for the treatment of inflammatory and autoimmune diseases. Another approach is the development of S1P-scavenging or -clearing agents, including a monoclonal S1P antibody that has successfully passed phase I clinical trials and will be further developed for age-related macular degeneration.
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