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临床试验/JPRN-UMIN000041546
JPRN-UMIN000041546已完成未知

Effect of daprodustat on renal anemia in patients with chronic kidney disease - Effect of daprodustat on renal anemia

Saitama Tsukinomori Clinic0 个研究点目标入组 10 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
10

研究概览

简要总结

The median dose of darbepoetin before switching was 40 micrograms/wk, and all subjects received daprodustat 4 mg orally once daily at the time of switching. After that, the dose of daprodustat was adjusted appropriately to achieve the guideline target Hb of 10-12g/dL. Hb was 10.9 + 0.4(SE)g/dL when switched to daprodustat. Hb levels did not change significantly until 12 months and were maintained at 10-12g/dL.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 90years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients complicated with serious diseases such as malignancy, heart failure (NYHA III degrees or more), and liver cirrhosis

研究者

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