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临床试验/NCT01227616
NCT01227616已完成4 期

Ferumoxytol for Anemia of CKD Trial (FACT): A Phase IV, Open-Label, Multicenter Trial, With MRI Substudy, of Repeated Doses of Ferumoxytol Compared With Iron Sucrose for Treatment of IDA in CKD Patients on Hemodialysis

AMAG Pharmaceuticals, Inc.3 个研究点 分布在 2 个国家目标入组 296 人开始时间: 2013年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
296
试验地点
3
主要终点
Hemoglobin Changes

研究概览

简要总结

The objectives of this study are to compare the efficacy and safety of repeat doses of intravenous (IV) ferumoxytol with IV iron sucrose for the treatment of IDA in subjects with hemodialysis-dependent CKD.

详细描述

This was a Phase IV, randomized, open-label, active-controlled, multicenter clinical trial designed to evaluate the safety, efficacy, and frequency of use of ferumoxytol compared to iron sucrose for the episodic treatment of IDA in hemodialysis subjects with CKD over a 1-year period. As part of this Main Study, an Oxidative Stress Substudy and an MRI Substudy were conducted. The Oxidative Stress Substudy, to be run concurrently with the initial TP of the Main Study, was to examine the varying degrees to which iron sucrose and ferumoxytol may or may not induce oxidative stress in vitro in subjects undergoing hemodialysis. The MRI Substudy, to be run concurrently with the Main Study and continue for an additional 11 months, was to assess the potential for deposition of iron in cardiac, hepatic, and pancreatic tissues and changes in laboratory parameters over a 2-year period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Ferumoxytol

Experimental

Intravenous (IV) iron

干预措施: Ferumoxytol (Drug)

IV Iron Sucrose

Active Comparator

Intravenous (IV) iron

干预措施: Iron Sucrose (Drug)

结局指标

主要结局

Hemoglobin Changes

时间窗: Up to 6 treatment periods (5 weeks per treatment period)

Changes in the mean hemoglobin between Baseline and Week 5 for ferumoxytol and iron sucrose in each treatment period.

次要结局

  • Changes in Transferrin Saturation (TSAT)(Up to 6 treatment periods (5 weeks per treatment period))
  • Proportion of Subjects With an Increase in Hemoglobin of ≥1.0 g/dL at Any Time From TP Baseline to Week 5 for Each TP(Up to 6 treatment periods (5 weeks per treatment period))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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