About Familial paroxysmal ataxia
Familial paroxysmal ataxia is a rare disease catalogued by Orphanet (ORPHA:97). It is associated with the CACNA1A 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 Familial paroxysmal ataxia trials.
Search ClinicalTrials.gov for "Familial paroxysmal ataxia" or filter by Orphanet code ORPHA:97 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 Familial paroxysmal ataxia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial paroxysmal ataxia. Updated daily.