About Neonatal ichthyosis-sclerosing cholangitis syndrome
Neonatal ichthyosis-sclerosing cholangitis syndrome is a rare disease catalogued by Orphanet (ORPHA:59303). It is associated with the CLDN1 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 Neonatal ichthyosis-sclerosing cholangitis syndrome trials.
Search ClinicalTrials.gov for "Neonatal ichthyosis-sclerosing cholangitis syndrome" or filter by Orphanet code ORPHA:59303 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 Neonatal ichthyosis-sclerosing cholangitis syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Neonatal ichthyosis-sclerosing cholangitis syndrome. Updated daily.