About Cockayne syndrome type 3
Cockayne syndrome type 3 is a rare disease catalogued by Orphanet (ORPHA:90324). It is associated with the ERCC6, ERCC8 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 Cockayne syndrome type 3 trials.
Search ClinicalTrials.gov for "Cockayne syndrome type 3" or filter by Orphanet code ORPHA:90324 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 Cockayne syndrome type 3 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Cockayne syndrome type 3. Updated daily.