About Pseudo-von Willebrand disease
Pseudo-von Willebrand disease is a rare disease catalogued by Orphanet (ORPHA:52530). It is associated with the GP1BA 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 Pseudo-von Willebrand disease trials.
Search ClinicalTrials.gov for "Pseudo-von Willebrand disease" or filter by Orphanet code ORPHA:52530 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 Pseudo-von Willebrand disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Pseudo-von Willebrand disease. Updated daily.