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慢性貧血および輸血性ヘモジデローシス患者におけるデフェラシロクスの有効性と安全性
基本情報
- NCT ID
- NCT00631163
- ステータス
- 完了
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 102
- 治験依頼者名
- Novartis
概要
The overall purpose of this trial is to further evaluate the efficacy and safety of deferasirox, dosed initially according to the transfusional iron intake, in patients with transfusion dependant anemia related to disorders other than β-thalassemia and sickle cell disease. During the study, the dose will be adjusted based on serum Ferritin.The overall purpose of the extension is to allow further treatment of patients who have already completed the core study, and to enable collection of long term efficacy and safety data. Patients will continue to receive Deferasirox at the dose they received at the end of the core study.
対象疾患
Chronic AnemiaTransfusional Hemosiderosis
介入
Deferasirox (ICL670)(DRUG)
依頼者(Sponsor)
ノバルティスファーマ株式会社(INDUSTRY)