跳至主要内容
临床试验/EUCTR2004-004499-35-HU
EUCTR2004-004499-35-HU进行中(未招募)不适用

A Study to Evaluate the Efficacy of Converting from Intravenous or Subcutaneous rHuEPO to Intravenous Darbepoetin Alfa (Aranesp®) in Subjects with Chronic Kidney Disease Receiving Haemodialysis

Amgen Limited0 个研究点目标入组 200 人开始时间: 2005年1月25日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Amgen Limited
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • · Diagnosis of CKD and receiving dialysis for at least 3 months prior to screening
  • · = 18 years of age
  • · Baseline Hb level = 10.0 g/dL and = 13.0 g/dL
  • · Adequate iron stores (defined as serum ferritin >100 µg/L or transferrin saturation (TSAT) > 20%)
  • · Stable IV (Epoetin alfa or beta) or SC rHuEPO (Epoetin beta) therapy 2 or 3 times per week for at least 8 weeks before screening (stable is defined as < 25% change in weekly dose and no change in frequency or route)
  • · Before any study-specific procedure, the appropriate written informed consent must be obtained (see Section 12.1).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • · Received SC Epoetin alpha in the 12 months before screening
  • · Uncontrolled hypertension (diastolic blood pressure > 100 mm Hg or systolic blood pressure > 180 mmHg on 2 separate occasions during screening)
  • · Prior history (within 12 weeks before enrolment) of cardiovascular events including:
  • - acute myocardial ischemia
  • - hospitalization for congestive heart failure
  • - myocardial infarction
  • · Pregnant or breast-feeding women. All subjects must practice adequate contraception (in the judgment of the investigator) throughout this trial.
  • · Treatment with an investigational agent or device within 30 days before screening or scheduled to receive an investigational agent other than those specified by this protocol during the course of this study.
  • · Known sensitivity to any of the products to be administered during dosing.
  • · Disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures.

研究者

发起方
Amgen Limited

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