About Marfan syndrome type 1
Marfan syndrome type 1 is a rare disease catalogued by Orphanet (ORPHA:284963). It is associated with the FBN1 gene. 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 Marfan syndrome type 1 trials.
Search ClinicalTrials.gov for "Marfan syndrome type 1" or filter by Orphanet code ORPHA:284963 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 Marfan syndrome type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Marfan syndrome type 1. Updated daily.