About Digenic Alport syndrome
Digenic Alport syndrome is a rare disease catalogued by Orphanet (ORPHA:653722). It is associated with the COL4A3, COL4A4, COL4A5 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 Digenic Alport syndrome trials.
Search ClinicalTrials.gov for "Digenic Alport syndrome" or filter by Orphanet code ORPHA:653722 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 Digenic Alport syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Digenic Alport syndrome. Updated daily.