About Hereditary late-onset Parkinson disease
Hereditary late-onset Parkinson disease is a rare disease catalogued by Orphanet (ORPHA:411602). It is associated with the SNCA, GBA1, LRRK2 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 Hereditary late-onset Parkinson disease trials.
Search ClinicalTrials.gov for "Hereditary late-onset Parkinson disease" or filter by Orphanet code ORPHA:411602 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 Hereditary late-onset Parkinson disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary late-onset Parkinson disease. Updated daily.