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Obeticholic acid

Generic Name
Obeticholic acid
Brand Names
Ocaliva
Drug Type
Small Molecule
Chemical Formula
C26H44O4
CAS Number
459789-99-2
Unique Ingredient Identifier
0462Z4S4OZ
Background

Primary biliary cirrhosis, or PBC, is a progressive and chronic condition that leads to hepatic injury often resulting in end-stage liver failure that requires liver transplantation.

Obeticholic acid is a farnesoid-X receptor (FXR) agonist used to treat this condition, possibly allowing for increased survival. In 2016, it was granted approval to treat primary biliary cholangitis in combination with ursodeoxycholic acid, which was previously the mainstay treatment for this condition. In May 2021, the FDA updated its prescribing information to contraindicate the use of obeticholic acid in patients with PBC and advanced cirrhosis (e.g. those with portal hypertension or hepatic decompensation) due to a risk of liver failure, in some cases requiring liver transplantation.

Obeticholic acid is currently being considered for FDA approval to treat fibrosis caused by non-alcoholic liver steatohepatitis (NASH). The NDA from Intercept Pharmaceuticals was approved in November 2019 and obeticholic acid is expected to be granted full approval for this indication in 2020.

Indication

用于治疗原发性胆汁性胆管炎(PBC)或用于治疗原发性胆汁性肝硬化(PBC)。

Associated Conditions
Primary Biliary Cholangitis

The Farnesoid X Receptor (FXR) Ligand Obeticholic Acid in NASH Treatment Trial(FLINT)

Phase 2
Completed
Conditions
Nonalcoholic Fatty Liver Disease (NAFLD)
Nonalcoholic Steatohepatitis (NASH)
Interventions
First Posted Date
2010-12-23
Last Posted Date
2018-04-06
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Target Recruit Count
283
Registration Number
NCT01265498
Locations
🇺🇸

Duke University Medical Center, Durham, North Carolina, United States

🇺🇸

Cleveland Clinic Foundation, Cleveland, Ohio, United States

🇺🇸

University of California, San Diego, San Diego, California, United States

and more 6 locations

Study of INT 747 in Combination With URSO in Patients With Primay Biliary Cirrhosis (PBC)

Phase 2
Terminated
Conditions
Liver Cirrhosis, Biliary
Interventions
Drug: Ursodeoxycholic Acid (URSO)
Drug: Placebo
First Posted Date
2007-10-30
Last Posted Date
2024-02-06
Lead Sponsor
Intercept Pharmaceuticals
Target Recruit Count
165
Registration Number
NCT00550862
Locations
🇺🇸

Henry Ford Health Center Columbus, Novi, Michigan, United States

🇺🇸

Baylor College of Medicine, Houston, Texas, United States

🇺🇸

U Florida Hepatology, Gainesville, Florida, United States

and more 29 locations

Study of INT-747 in Patients With Diabetes and Presumed NAFLD

Phase 2
Completed
Conditions
Diabetes Mellitus, Type II
Fatty Liver
Interventions
Drug: Placebo
First Posted Date
2007-07-16
Last Posted Date
2012-04-20
Lead Sponsor
Intercept Pharmaceuticals
Target Recruit Count
64
Registration Number
NCT00501592
Locations
🇺🇸

Profil Institute for Clinical Research, Inc., Chula Vista, California, United States

🇺🇸

UC San Diego VAMC, San Diego, California, United States

🇺🇸

Virginia Commonwelath University, Richmond, Virginia, United States

and more 1 locations
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