About Familial isolated trichomegaly
Familial isolated trichomegaly is a rare disease catalogued by Orphanet (ORPHA:411788). It is associated with the FGF5 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 Familial isolated trichomegaly trials.
Search ClinicalTrials.gov for "Familial isolated trichomegaly" or filter by Orphanet code ORPHA:411788 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 isolated trichomegaly trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial isolated trichomegaly. Updated daily.