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临床试验/JPRN-jRCT2080221341
JPRN-jRCT2080221341未知3 期

A clinical study of KRN321 in pediatric patients with chronic kidney disease

Kyowa Hakko Kirin Co., Ltd.0 个研究点开始时间: 2010年12月24日最近更新:
适应症

试验速览

阶段
3 期
发起方

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
>= 2age old 至 <= 18age old(—)
性别
All

入选标准

  • Written informed consent from guardian
  • - ND patients (diagnosed with CKD and not receiving hemodialysis), PD patients (receiving peritoneal dialysis), or HD patients (receiving hemodialysis once a week or over)

排除标准

  • - Uncontrolled hypertension
  • - Congestive heart failure
  • - Malignant tumor, hematological disease or hemorrhagic lesion
  • - Within 16 weeks preceding the study, excessive bleeding or blood transfusion associated with surgical operation etc.
  • - Serious allergy (include drug hypersensitivity)
  • - Hypersensitivity for rHuEPO agents

研究者

发起方
Kyowa Hakko Kirin Co., Ltd.

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