About Diffuse cutaneous systemic sclerosis
Diffuse cutaneous systemic sclerosis is a rare disease catalogued by Orphanet (ORPHA:220393). It is associated with the CAV1, HLA-DRB1, CCN2 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 Diffuse cutaneous systemic sclerosis trials.
Search ClinicalTrials.gov for "Diffuse cutaneous systemic sclerosis" or filter by Orphanet code ORPHA:220393 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 Diffuse cutaneous systemic sclerosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Diffuse cutaneous systemic sclerosis. Updated daily.