Topical 'dual-soft' glucocorticoid receptor agonist for dermatology

被引:6
作者
Dack, Kevin N. [1 ]
Johnson, Patrick S. [1 ]
Henriksson, Krister [1 ]
Eirefelt, Stefan [1 ]
Carnerup, Martin A. [1 ]
Stahlhut, Martin [1 ]
Ollerstam, Anna K. [2 ]
机构
[1] LEO Pharma AS, Ind Pk 55, DK-2750 Ballerup, Denmark
[2] AstraZeneca, Lab Anim Sci Drug Safety & Metab, IMED Biotech Unit, Pepparedsleden 1, Molndal, Sweden
关键词
Dermatology; Non-steroidal; SEGRA; Soft-drug; Glucocorticoid receptor agonist;
D O I
10.1016/j.bmcl.2020.127402
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Steroidal glucocorticoids (GR agonists) have been widely used for the topical treatment of skin disorders, including atopic dermatitis. They are a very effective therapy, but they are associated with both unwanted local effects in the skin (skin thinning/atrophy) and systemic side effects. These effects can limit the long-term utility of potent steroids. Here we report on a topically delivered non-steroidal GR agonist, that has the potential to deliver high efficacy in the skin, but due to rapid metabolism in the blood & liver ("dual-soft") it should have greater systemic safety than existing treatments. In addition, compared to less selective steroidal GR agonists, the new nonsteroidal Selective Glucocorticoid Agonists (SEGRAs) have the potential to avoid the skin atrophy observed with existing topical steroids. Due to its potential for reduced skin atrophy and low systemic exposure, LEO 134310 (17) may be suitable for long term topical treatment of skin diseases such as atopic dermatitis and psoriasis.
引用
收藏
页数:4
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