About Familial patent arterial duct
Familial patent arterial duct is a rare disease catalogued by Orphanet (ORPHA:466729). It is associated with the TFAP2B, PRDM6 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 Familial patent arterial duct trials.
Search ClinicalTrials.gov for "Familial patent arterial duct" or filter by Orphanet code ORPHA:466729 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 Familial patent arterial duct trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial patent arterial duct. Updated daily.