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 |