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To investigate safety and efficacy on Japanese subjects treated with nelarabine injection for intravenous use in clinical settings of the following diseases:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Subjects administered nelarabine | Subjects with T-cell acute lymphocytic leukemia (T-ALL) or T-cell lymphoblastic lymphoma (T-LBL) prescribed nelarabine during study period |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Nelarabine | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| The number of adverse events in Japanese subjects treated with nelarabine based on prescribing information under the conditions of general clinical practice. | 1 year | |
| Any incidence of adverse events related to neurological disorder, hypotension, and blood disorder and their details | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Outcome (alive or dead) at one year after the start of treatment | 1 year |
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Inclusion Criteria:
Exclusion Criteria:
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Subjects with the following diseases in Japanese adults and children
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Tsukuba Hospital | Tsukuba | Japan |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| C104457 | nelarabine |
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