About Persistent hyperplastic primary vitreous
Persistent hyperplastic primary vitreous is a rare disease catalogued by Orphanet (ORPHA:91495). It is associated with the FZD4, NDP, ATOH7 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 Persistent hyperplastic primary vitreous trials.
Search ClinicalTrials.gov for "Persistent hyperplastic primary vitreous" or filter by Orphanet code ORPHA:91495 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 Persistent hyperplastic primary vitreous trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Persistent hyperplastic primary vitreous. Updated daily.