About Benign recurrent intrahepatic cholestasis type 1
Benign recurrent intrahepatic cholestasis type 1 is a rare disease catalogued by Orphanet (ORPHA:99960). It is associated with the ATP8B1 gene. 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 Benign recurrent intrahepatic cholestasis type 1 trials.
Search ClinicalTrials.gov for "Benign recurrent intrahepatic cholestasis type 1" or filter by Orphanet code ORPHA:99960 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
Find recruiting Benign recurrent intrahepatic cholestasis type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Benign recurrent intrahepatic cholestasis type 1. Updated daily.