Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e91879cb29d51c1dd6f6db9674957c9c http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_17b367e96fc1b9afd2c403b58f550cf4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_adc048c2a637cc5389e0118ca5b5f27a http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e040a90fcc5784074adcc886b526c448 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P17-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-575 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-575 |
filingDate |
2016-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2019-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2b2a203b55f5e510b32b6dd786de030 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d629506868ad7015fe29f9e8dc9ed6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f1ffc7779995df2d1aab90f5390ead2c |
publicationDate |
2019-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-10258633-B2 |
titleOfInvention |
Treatment of fibrosis using FXR ligands |
abstract |
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. |
priorityDate |
2004-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |