Treatment of fibrosis using FXR ligands
US-9498484-B2 · Nov 22, 2016 · US
US10987362B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10987362-B2 |
| Application number | US-201816228944-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 21, 2018 |
| Priority date | Mar 12, 2004 |
| Publication date | Apr 27, 2021 |
| Grant date | Apr 27, 2021 |
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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.
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What is claimed is: 1. A method for treating non-alcoholic steatohepatitis in a subject not suffering from a cholestatic condition, the method comprising the step of administering to the subject an effective amount of tauro-6-ethyl-chenodeoxycholic acid (tauro-6ECDCA). 2. The method of claim 1 , wherein tauro-6ECDCA is administered at a daily dose of 5-500 mg orally. 3. The method of claim 1 , wherein the cholestatic condition is defined as having abnormally elevated serum levels of alkaline phosphatase, γ-glutamyl transpeptidase (GGT), and 5′ nucleotidase. 4. The method of claim 3 , wherein the cholestatic condition is further defined as presenting with at least one clinical symptom. 5. The method of claim 4 , wherein the symptom is itching (pruritus).
Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title
for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics · CPC title
substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol · CPC title
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