发明名称 Treatment of fibrosis using FXR ligands
摘要 The present invention relates to a method for inhibiting fibrosis that occurs in an organ where the farnesoid X receptor (FXR) is expressed. This method involves the step of administering a high potency, activating ligand of FXR in an effective amount to a patient who is not suffering from a cholestatic condition. The invention also provides pharmaceutical compositions containing an effective amount of an FXR ligand and kits for dispensing the pharmaceutical compositions.
申请公布号 US9498484(B2) 申请公布日期 2016.11.22
申请号 US200511081002 申请日期 2005.03.14
申请人 Intercept Pharmaceuticals, Inc. 发明人 Fiorucci Stefano;Pellicciari Roberto;Pruzanski Mark
分类号 A61K31/56 主分类号 A61K31/56
代理机构 Cooley LLP 代理人 Cooley LLP ;Elrifi Ivor R.;Erlacher Heidi A.
主权项 1. A method of treating liver fibrosis in a human not suffering from a cholestatic condition, comprising the steps of selecting a human who is not suffering from a cholestatic condition and administering to the human 6-ethyl-chenodeoxycholic acid at a daily dose of 5-500 mg orally.
地址 New York NY US