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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Longitudinal Study of the PorphyriasCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Coproporphyria, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, acute intermittent porphyria, erythropoietic protoporphyria, hepatic porphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, skin disorderRecruitingNot stated2026-05-15NCT01561157