hereditary coproporphyria
hereditary coproporphyria
Explore linked clinical trials. Standard reference: MONDO:00073693 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| ELEVATE, a Registry of Patients With Acute Hepatic Porphyria (AHP) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, hepatic porphyria, hereditary coproporphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, porphyria, porphyria due to ALA dehydratase deficiency, skin disorder | Recruiting | Not stated | 2026-10-06 | NCT04883905 | |
| Evaluating the Prevalence of Acute Hepatic Porphyria in Postural Tachycardia Syndrome | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, autonomic nervous system disorder, hepatic porphyria, hereditary coproporphyria, hereditary disease, hereditary skin disorder, liver disorder, metabolic disease, nervous system disorder, orthostatic intolerance, porphyria, porphyria due to ALA dehydratase deficiency, primary dysautonomia, skin disorder | Active, not recruiting | Not stated | 2026-09-28 | NCT05344599 | |
| 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 |