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ARRANON G(ネララビン)注射剤250mgの薬物使用調査
基本情報
- NCT ID
- NCT01376115
- ステータス
- 完了
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 343
- 治験依頼者名
- Novartis
概要
To investigate safety and efficacy on Japanese subjects treated with nelarabine injection for intravenous use in clinical settings of the following diseases: 1. T-cell acute lymphocytic leukemia (T-ALL) 2. T-cell lymphoblastic lymphoma (T-LBL) Also, "any adverse events involving neurological disorder, hypotension, and blood disorder and their details" are to be investigated as an item of particular concern. In addition, subject outcome (alive or dead) at one year after the start of treatment will also be investigated.
対象疾患
Cancer
介入
Nelarabine(DRUG)
依頼者(Sponsor)
ノバルティスファーマ株式会社(INDUSTRY)
実施施設 (1)
筑波大学附属病院
Tsukuba, Japan