About Typical urticaria pigmentosa
Typical urticaria pigmentosa is a rare disease catalogued by Orphanet (ORPHA:158766). It is associated with the KIT 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 Typical urticaria pigmentosa trials.
Search ClinicalTrials.gov for "Typical urticaria pigmentosa" or filter by Orphanet code ORPHA:158766 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 Typical urticaria pigmentosa trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Typical urticaria pigmentosa. Updated daily.