About Hereditary mixed polyposis syndrome
Hereditary mixed polyposis syndrome is a rare disease catalogued by Orphanet (ORPHA:157794). It is associated with the BMPR1A, GREM1 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 Hereditary mixed polyposis syndrome trials.
Search ClinicalTrials.gov for "Hereditary mixed polyposis syndrome" or filter by Orphanet code ORPHA:157794 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 Hereditary mixed polyposis syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Hereditary mixed polyposis syndrome. Updated daily.