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临床试验/JPRN-UMIN000024750
JPRN-UMIN000024750已完成未知

Studies of efficacy and safety of simultaneous administration of febuxostat and inosine for patients with genetic anemia, and changes of blood and urine purine compounds - Effect of febuxostat and inosine on anemia

Tsukuba International Clinical Pharmacology Clinic0 个研究点目标入组 6 人开始时间: 2017年2月27日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Subjects taking azathioprine or mercaptopurine 2.Subject who has or had renal function disorder. 3.Subject with a history of gout, hyperuricemia or urolithiasis. 4.Subject who has or had hypersensitivity, idiosyncracy (allergy) to drug. 5.Subjects to whom either transfusion or surgical treatment such as splenectomy was made within 3 months before the initiation of the drug therapy. 6.Subject who was judged not to be appropriate by the principal investigator or sub investigators by other reasons.

研究者

发起方
Tsukuba International Clinical Pharmacology Clinic

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