Lysosomal Acid Lipase (LAL) Deficiency Registry
Lysosomal Acid Lipase (LAL) Deficiency Registry
Recruiting · NCT01633489 · Registry updated 2026-03-06Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Lysosomal Acid Lipase (LAL) Deficiency Registry | Acid Cholesteryl Ester Hydrolase Deficiency, Type 2, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Infant, Newborn, Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Wolman disease, cholesteryl ester storage disease, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease | Recruiting | Not stated | 2026-03-06 | NCT01633489 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Alexion Pharmaceuticals, Inc. | 48 |
0 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| No products are listed yet. | |||