About Congenital mesoblastic nephroma
Congenital mesoblastic nephroma is a rare disease catalogued by Orphanet (ORPHA:2665). It is associated with the ETV6, NTRK3 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 Congenital mesoblastic nephroma trials.
Search ClinicalTrials.gov for "Congenital mesoblastic nephroma" or filter by Orphanet code ORPHA:2665 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 Congenital mesoblastic nephroma trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital mesoblastic nephroma. Updated daily.