Identification of Acute Intermittent Porphyria Modifying Genes
Identification of Acute Intermittent Porphyria Modifying Genes
Recruiting · NCT05502133 · Registry updated 2026-09-10Clinical trials
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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 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Icahn School of Medicine at Mount Sinai | 256 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Icahn School of Medicine at Mount Sinai | New York | United States | 342 |