About Peters anomaly
Peters anomaly is a rare disease catalogued by Orphanet (ORPHA:708). It is associated with the FOXC1, CYP1B1, PITX2 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 Peters anomaly trials.
Search ClinicalTrials.gov for "Peters anomaly" or filter by Orphanet code ORPHA:708 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 Peters anomaly trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Peters anomaly. Updated daily.