About Annular epidermolytic ichthyosis
Annular epidermolytic ichthyosis is a rare disease catalogued by Orphanet (ORPHA:281139). It is associated with the KRT10, KRT1 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 Annular epidermolytic ichthyosis trials.
Search ClinicalTrials.gov for "Annular epidermolytic ichthyosis" or filter by Orphanet code ORPHA:281139 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 Annular epidermolytic ichthyosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Annular epidermolytic ichthyosis. Updated daily.