About Primary familial polycythemia
Primary familial polycythemia is a rare disease catalogued by Orphanet (ORPHA:90042). It is associated with the EPOR 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 Primary familial polycythemia trials.
Search ClinicalTrials.gov for "Primary familial polycythemia" or filter by Orphanet code ORPHA:90042 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 Primary familial polycythemia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary familial polycythemia. Updated daily.