Study of Velaglucerase Beta ERT in Children With Gaucher Disease
Study of Velaglucerase Beta ERT in Children With Gaucher Disease
Not yet recruiting · NCT07847411 · Registry updated 2026-09-29Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Study of Velaglucerase Beta ERT in Children With Gaucher Disease | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Gaucher Disease, Type 1, Gaucher Disease, Type 3, Gaucher disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis | Not yet recruiting | Phase 3 | 2026-09-29 | NCT07847411 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| CANbridge Life Sciences Ltd. | 1 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Room 202, 2nd Floor, 780 Cailun Road, Pilot Free Trade Zone | Shanghai | China | 1 |