About Simpson-Golabi-Behmel syndrome
Simpson-Golabi-Behmel syndrome is a rare disease catalogued by Orphanet (ORPHA:373). It is associated with the GPC3, GPC4 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 Simpson-Golabi-Behmel syndrome trials.
Search ClinicalTrials.gov for "Simpson-Golabi-Behmel syndrome" or filter by Orphanet code ORPHA:373 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 Simpson-Golabi-Behmel syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Simpson-Golabi-Behmel syndrome. Updated daily.