Treatment of fibrosis using FXR ligands

US10987362B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10987362-B2
Application numberUS-201816228944-A
CountryUS
Kind codeB2
Filing dateDec 21, 2018
Priority dateMar 12, 2004
Publication dateApr 27, 2021
Grant dateApr 27, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

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).

Assignees

Inventors

Classifications

  • Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title

  • A61P1/16Primary

    for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics · CPC title

  • A61K31/575Primary

    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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What does patent US10987362B2 cover?
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 a…
Who is the assignee on this patent?
Intercept Pharmaceuticals Inc
What technology area does this patent fall under?
Primary CPC classification A61P1/16. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Apr 27 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).