About CLN12 disease
CLN12 disease is a rare disease catalogued by Orphanet (ORPHA:314632). It is associated with the ATP13A2 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 CLN12 disease trials.
Search ClinicalTrials.gov for "CLN12 disease" or filter by Orphanet code ORPHA:314632 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 CLN12 disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for CLN12 disease. Updated daily.