Disease Directory Primary biliary cholangitis
Rare Disease

Primary biliary cholangitis

Type

Disease

Gene

IL12RB1, SPIB, IL12A, IRF5, TNPO3, MMEL1

About Primary biliary cholangitis

Primary biliary cholangitis is a rare disease catalogued by Orphanet (ORPHA:186). It is associated with the IL12RB1, SPIB, IL12A genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Primary biliary cholangitis trials.

Search ClinicalTrials.gov for "Primary biliary cholangitis" or filter by Orphanet code ORPHA:186 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:186)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Primary biliary cholangitis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary biliary cholangitis. Updated daily.