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临床试验/LBCTR2020011375
LBCTR2020011375已完成4 期

An Open Label, Multi-center, Efficacy and Safety Study of Deferasirox in Iron Overloaded Patients With Non-transfusion Dependent Thalassemia

ovartis Pharmaceuticals0 个研究点目标入组 20 人开始时间: 2020年1月7日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
10 至 99(—)
性别
All

入选标准

  • Non-transfusion dependent congenital or chronic anemia inclusive of beta-thalassemia intermedia, HbE beta-thalassemia or alpha-thalassemia intermedia (HbH disease)/ Liver iron concentration >/= 5 mg Fe/g dw Serum Ferritin >/= 300 ng/m

排除标准

  • HbS-beta Thalassemia, anticipated regular transfusion program during the study, blood transfusion 6 months prior to study start, significant proteinuria..

研究者

发起方
ovartis Pharmaceuticals

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