About FG syndrome type 1
FG syndrome type 1 is a rare disease catalogued by Orphanet (ORPHA:93932). It is associated with the MED12 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 FG syndrome type 1 trials.
Search ClinicalTrials.gov for "FG syndrome type 1" or filter by Orphanet code ORPHA:93932 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 FG syndrome type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for FG syndrome type 1. Updated daily.