About Classic progressive supranuclear palsy syndrome
Classic progressive supranuclear palsy syndrome is a rare disease catalogued by Orphanet (ORPHA:240071). It is associated with the MAPT 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 Classic progressive supranuclear palsy syndrome trials.
Search ClinicalTrials.gov for "Classic progressive supranuclear palsy syndrome" or filter by Orphanet code ORPHA:240071 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 Classic progressive supranuclear palsy syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Classic progressive supranuclear palsy syndrome. Updated daily.