acute intermittent porphyria | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Identification of Acute Intermittent Porphyria Modifying Genes	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, acute intermittent porphyria, hepatic porphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, skin disorder	Recruiting	Not stated	2026-09-10		NCT05502133
Longitudinal Study of the Porphyrias	Congenital, 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 disorder	Recruiting	Not stated	2026-05-15		NCT01561157
Acute Porphyria Biomarkers for Disease Activity	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, acute intermittent porphyria, hepatic porphyria, hereditary coproporphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, skin disorder, variegate porphyria	Active, not recruiting	Not stated	2026-05-12		NCT02935400
Clinical Research on Acute Intermittent Porphyria and the Use of Carbohydrate-Rich Diet as a Treatment	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, acute intermittent porphyria, hepatic porphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, skin disorder	Recruiting	Not applicable	2026-03-27		NCT06273644