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The purpose of this study is to evaluate the safety and efficacy of ISU302 in patients with Type 1 Gaucher disease previously treated with Imiglucerase.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ISU302 | 15~60U/kg (once every 2 weeks for 6 months) |
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| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with Adverse Events | To evaluate the safety of ISU302 in patients with Type 1 Gaucher disease previously treated with Cerezyme® after administering ISU302 alternative to Cerezyme® | From Screening to Week 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Pharmacokinetics | Measurement of blood glucocerebrosidase activity for pharmacokinetic assessment after initial study drug administration | From Screening to Week 24 |
| hemoglobin concentration | Change in hemoglobin concentration |
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Inclusion Criteria:
Patient diagnosed with type-1 Gaucher disease
Patient who was stably treating Gaucher disease with Cerezyme® and who was maintaining the usage and dosage of Cerezyme® for at least 6 months prior to study drug administration
Patient aged 2 years or higher
Female patient with contraception during the study period (oral or injectable contraceptive hormones, intrauterine device, physical devices using condom, sponge form, jelly, and femidom, and abstinence)
Patient who signed the informed consent form after hearing the detailed explanation about this study
No neurologic deficit
Normal hemoglobin concentration, and platelet count that has increased to ≥100,000/㎣, or maintained to 100,000/㎣
Normal or no deteriorated bone mineral density
Normal or no deteriorated splenomegaly or hepatomegaly
Exclusion Criteria:
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Patient diagnosed with type-1 Gaucher disease
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25829804 | Derived | Choi JH, Lee BH, Ko JM, Sohn YB, Lee JS, Kim GH, Heo SH, Park JY, Kim YM, Kim JH, Yoo HW. A phase 2 multi-center, open-label, switch-over trial to evaluate the safety and efficacy of Abcertin(R) in patients with type 1 Gaucher disease. J Korean Med Sci. 2015 Apr;30(4):378-84. doi: 10.3346/jkms.2015.30.4.378. Epub 2015 Mar 19. |
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| ID | Term |
|---|---|
| D005776 | Gaucher Disease |
| ID | Term |
|---|---|
| D013106 | Sphingolipidoses |
| D020140 | Lysosomal Storage Diseases, Nervous System |
| D020739 | Brain Diseases, Metabolic, Inborn |
| D001928 | Brain Diseases, Metabolic |
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| From Screening to Week 24 |
| platelet count | Change in platelet count | From Screening to Week 24 |
| liver and spleen volumes and liver function | Changes in liver and spleen volumes and liver function | From Screening to Week 24 |
| biomarker levels | Changes in biomarker levels (Acid Phosphatase, Angiotensin Converting Enzyme, and Chitotriosidase) | From Screening to Week 24 |
| skeletal status and bone mineral density | Changes in skeletal status and bone mineral density | From Screening to Week 24 |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D008064 | Lipidoses |
| D008052 | Lipid Metabolism, Inborn Errors |
| D016464 | Lysosomal Storage Diseases |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D052439 | Lipid Metabolism Disorders |