About Pustulosis palmaris et plantaris
Pustulosis palmaris et plantaris is a rare disease catalogued by Orphanet (ORPHA:163927). It is associated with the IL36RN, AP1S3 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 Pustulosis palmaris et plantaris trials.
Search ClinicalTrials.gov for "Pustulosis palmaris et plantaris" or filter by Orphanet code ORPHA:163927 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 Pustulosis palmaris et plantaris trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Pustulosis palmaris et plantaris. Updated daily.