About Limited cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis is a rare disease catalogued by Orphanet (ORPHA:220402). 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 Limited cutaneous systemic sclerosis trials.
Search ClinicalTrials.gov for "Limited cutaneous systemic sclerosis" or filter by Orphanet code ORPHA:220402 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 Limited cutaneous systemic sclerosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Limited cutaneous systemic sclerosis. Updated daily.