About Congenital factor XI deficiency
Congenital factor XI deficiency is a rare disease catalogued by Orphanet (ORPHA:329). It is associated with the F11 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 Congenital factor XI deficiency trials.
Search ClinicalTrials.gov for "Congenital factor XI deficiency" or filter by Orphanet code ORPHA:329 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 Congenital factor XI deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital factor XI deficiency. Updated daily.