About Mal de Meleda
Mal de Meleda is a rare disease catalogued by Orphanet (ORPHA:87503). It is associated with the SLURP1 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 Mal de Meleda trials.
Search ClinicalTrials.gov for "Mal de Meleda" or filter by Orphanet code ORPHA:87503 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 Mal de Meleda trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Mal de Meleda. Updated daily.