About Combined deficiency of factor V and factor VIII
Combined deficiency of factor V and factor VIII is a rare disease catalogued by Orphanet (ORPHA:35909). It is associated with the MCFD2, LMAN1 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 Combined deficiency of factor V and factor VIII trials.
Search ClinicalTrials.gov for "Combined deficiency of factor V and factor VIII" or filter by Orphanet code ORPHA:35909 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 Combined deficiency of factor V and factor VIII trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Combined deficiency of factor V and factor VIII. Updated daily.