About Microvillus inclusion disease
Microvillus inclusion disease is a rare disease catalogued by Orphanet (ORPHA:2290). It is associated with the MYO5B, STX3 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 Microvillus inclusion disease trials.
Search ClinicalTrials.gov for "Microvillus inclusion disease" or filter by Orphanet code ORPHA:2290 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 Microvillus inclusion disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Microvillus inclusion disease. Updated daily.