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Biliary Cirrhosis, Primary clinical trials

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NCT ID: NCT02932449 Active, not recruiting - Clinical trials for Biliary Cirrhosis, Primary

A 5-year Longitudinal Observational Study of Patients With Primary Biliary Cholangitis

Start date: October 2016
Phase:
Study type: Observational

This is a 5-year, longitudinal, observational study of patients with PBC designed to specifically address important clinical questions that remain incompletely answered from registration trials. In addition to the study database, a bio specimen repository will also be included so that translational studies of genomics and biomarkers of response may be performed.

NCT ID: NCT02360852 Terminated - Clinical trials for Biliary Cirrhosis, Primary

IBAT Inhibitor A4250 for Cholestatic Pruritus

Start date: January 2015
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety, tolerability and influence on itching, bile acids and liver enzyme changes in patients with PBC (Primary Biliary Cirrhosis) treated with A4250

NCT ID: NCT00242125 Recruiting - Clinical trials for Biliary Cirrhosis, Primary

Family Studies in Primary Biliary Cirrhosis (PBC)

Start date: October 2005
Phase: N/A
Study type: Observational

Primary biliary cirrhosis (PBC) is a chronic liver disease primarily affecting middle age women. It is characterized by immune-mediated damage to cells lining the tiny bile ducts within the liver. Although the underlying cause of PBC is likely to be multifactorial, the epidemiologic/population data indicate a very important role for genetic predisposition, meaning that the disease seems to run in families. Susceptibility genes for PBC have not been identified possibly due to limitations such as small sample size in prior studies. The primary objective of this study is to identify these genes. This study involves obtaining clinical and demographic data as well as collecting DNA samples from patients and their parents, and siblings to screen for a select set of candidate genes as well as the full genome for variants associated with PBC.

NCT ID: NCT00145964 Recruiting - Clinical trials for Liver Cirrhosis, Biliary

Identification of the Genetic Variants Responsible for Primary Biliary Cirrhosis (PBC)

Start date: August 2004
Phase: N/A
Study type: Observational

Primary biliary cirrhosis (PBC) is a disease of the liver, which predominantly affects women. It causes slowly progressive liver disease, which eventually causes liver failure, requiring a liver transplant. Several different studies of large patient cohorts indicate that the cause of this disease is likely due to a combination of factors including genetic and environmental. PBC is associated with several other "autoimmune diseases" - recently a gene has been identified to be abnormal in individuals with another autoimmune liver disease, namely rheumatoid arthritis. This gene usually tells the body when to switch off an immune response. This study plans to identify whether individuals diagnosed with PBC have a similar abnormality in this gene called protein Tyrosine Phosphatase.