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| Found 14 studies with search of: | Tay-Sachs Disease |
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Unknown † |
A Natural History Study of Hexosaminidase Deficiency in Infantile Tay-Sachs Disease
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| 2 | Suspended |
A Phase I Study of Pyrimethamine in Patients With GM-2 Gangliosidosis
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| 3 | Completed |
Pyrimethamine as a Treatment for Late-Onset GM2-gangliosidosis (Tay-Sachs and Sandhoff Disease)
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| 4 | Unknown † |
Pharmacokinetics and Tolerability of Zavesca® (Miglustat) In Patients With Juvenile GM2 Gangliosidosis
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| 5 | Completed |
Pharmacokinetics, Safety and Tolerability of Zavesca (Miglustat) in Patients With Infantile Onset Gangliosidosis: Single and Steady State Oral Doses
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| 6 | Recruiting |
HSCT for High Risk Inherited Inborn Errors
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| 7 | Completed |
Diagnostic and Screening Study of Genetic Disorders
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| 8 |
Completed
Has Results |
Stem Cell Transplant for Inborn Errors of Metabolism
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| 9 | Suspended |
ALD-101 Adjuvant Therapy of Unrelated Umbilical Cord Blood Transfusion (UCBT) in Patients With Inherited Metabolic Diseases
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| 10 | Recruiting |
Nervous System Degeneration in Glycosphingolipid Storage Disorders
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| 11 | Recruiting |
Fetal Umbilical Cord Blood (UCB) Transplant for Lysosomal Storage Diseases
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| 12 | Active, not recruiting |
Concurrent Single Gene and 24 Chromosome Aneuploidy Preimplantation Genetic Diagnosis (PGD)
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| 13 | Recruiting |
Unrelated Umbilical Cord Blood Transplantation Augmented With ALDHbr Umbilical Cord Blood Cells
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| 14 | Active, not recruiting |
Clinical Use of Parental Support To Detect Single Gene Mutations
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