About Childhood absence epilepsy
Childhood absence epilepsy is a rare disease catalogued by Orphanet (ORPHA:64280). It is associated with the GABRA1, GABRG2, GABRB3 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 Childhood absence epilepsy trials.
Search ClinicalTrials.gov for "Childhood absence epilepsy" or filter by Orphanet code ORPHA:64280 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 Childhood absence epilepsy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Childhood absence epilepsy. Updated daily.