About Juvenile polyposis of infancy
Juvenile polyposis of infancy is a rare disease catalogued by Orphanet (ORPHA:79076). It is associated with the PTEN, BMPR1A 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 Juvenile polyposis of infancy trials.
Search ClinicalTrials.gov for "Juvenile polyposis of infancy" or filter by Orphanet code ORPHA:79076 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 Juvenile polyposis of infancy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Juvenile polyposis of infancy. Updated daily.