About Familial mesial temporal lobe epilepsy
Familial mesial temporal lobe epilepsy is a rare disease catalogued by Orphanet (ORPHA:163717). It is associated with the CPA6 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 mesial temporal lobe epilepsy trials.
Search ClinicalTrials.gov for "Familial mesial temporal lobe epilepsy" or filter by Orphanet code ORPHA:163717 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 mesial temporal lobe epilepsy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial mesial temporal lobe epilepsy. Updated daily.