About Vein of Galen malformation
Vein of Galen malformation is a rare disease catalogued by Orphanet (ORPHA:1053). It is associated with the EPHB4 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 Vein of Galen malformation trials.
Search ClinicalTrials.gov for "Vein of Galen malformation" or filter by Orphanet code ORPHA:1053 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 Vein of Galen malformation trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Vein of Galen malformation. Updated daily.