About Vici syndrome
Vici syndrome is a rare disease catalogued by Orphanet (ORPHA:1493). It is associated with the EPG5 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 Vici syndrome trials.
Search ClinicalTrials.gov for "Vici syndrome" or filter by Orphanet code ORPHA:1493 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 Vici syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Vici syndrome. Updated daily.