About Familial advanced sleep-phase syndrome
Familial advanced sleep-phase syndrome is a rare disease catalogued by Orphanet (ORPHA:164736). It is associated with the PER3, CSNK1D, PER2 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 Familial advanced sleep-phase syndrome trials.
Search ClinicalTrials.gov for "Familial advanced sleep-phase syndrome" or filter by Orphanet code ORPHA:164736 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 advanced sleep-phase syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial advanced sleep-phase syndrome. Updated daily.