About Congenital tufting enteropathy
Congenital tufting enteropathy is a rare disease catalogued by Orphanet (ORPHA:92050). It is associated with the EPCAM 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 Congenital tufting enteropathy trials.
Search ClinicalTrials.gov for "Congenital tufting enteropathy" or filter by Orphanet code ORPHA:92050 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 Congenital tufting enteropathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital tufting enteropathy. Updated daily.