About Primary CD59 deficiency
Primary CD59 deficiency is a rare disease catalogued by Orphanet (ORPHA:169464). It is associated with the CD59 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 CD59 deficiency trials.
Search ClinicalTrials.gov for "Primary CD59 deficiency" or filter by Orphanet code ORPHA:169464 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 CD59 deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary CD59 deficiency. Updated daily.