About Congenital erythropoietic porphyria
Congenital erythropoietic porphyria is a rare disease catalogued by Orphanet (ORPHA:79277). It is associated with the UROS, GATA1 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 Congenital erythropoietic porphyria trials.
Search ClinicalTrials.gov for "Congenital erythropoietic porphyria" or filter by Orphanet code ORPHA:79277 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 Congenital erythropoietic porphyria trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Congenital erythropoietic porphyria. Updated daily.