About Congenital factor X deficiency
Congenital factor X deficiency is a rare disease catalogued by Orphanet (ORPHA:328). It is associated with the F10 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 X deficiency trials.
Search ClinicalTrials.gov for "Congenital factor X deficiency" or filter by Orphanet code ORPHA:328 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 X deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital factor X deficiency. Updated daily.