About Curry-Jones syndrome
Curry-Jones syndrome is a rare disease catalogued by Orphanet (ORPHA:1553). It is associated with the SMO 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 Curry-Jones syndrome trials.
Search ClinicalTrials.gov for "Curry-Jones syndrome" or filter by Orphanet code ORPHA:1553 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 Curry-Jones syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Curry-Jones syndrome. Updated daily.