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临床试验/NCT01503736
NCT01503736已完成3 期

A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Definitive Phase III Study of the Effects of Ferric Citrate on Serum Phosphate in Subjects With End Stage Renal Disease

Panion & BF Biotech Inc.5 个研究点 分布在 1 个国家目标入组 183 人开始时间: 2010年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
183
试验地点
5
主要终点
Change in serum phosphorus at Day 56 as compared to baseline

研究概览

简要总结

The purpose of the study is to determine the effect and optimum dose and evaluate the safety of ferric citrate, administered three times daily (TID) immediately after meals for a total daily dose of 4 or 6 grams for 56 days, on serum phosphate (PO4) levels in subjects with end stage renal disease (ESRD).

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Age>18 years and has a diagnosis of ESRD
  • On a three-times per week hemodialysis regimen
  • On a stable dose of a phosphate-binding agent for at least one month prior to study entry.
  • If on vitamin D supplementation or calcitriol, must be on a stable dose for at least one month prior to study entry.
  • Hct >= 20%
  • Serum Ca level of 8 mg/dL to 10.5 mg/dL

排除标准

  • Is pregnant or lactating
  • Clinically significant GI disorder
  • Has tertiary hyperparathyroidism or is immediately post-operative from a parathyroidectomy (within the first 3 months post-op or the plasma Ca is <7 mg/dL)
  • ferritin>800 ng/mL
  • Unstable medical condition unsuitable for the study in the opinion of investigator
  • Has been treated with an investigational agent within 30 days of enrollment
  • Has a history of documented iron allergy or hemochromatosis

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: ferric citrate (Drug)

4g/day

Experimental

Ferric Citrate for a total daily dose of 4g

干预措施: ferric citrate (Drug)

6g/day

Experimental

Ferric Citrate for a total daily dose of 6g

干预措施: ferric citrate (Drug)

结局指标

主要结局

Change in serum phosphorus at Day 56 as compared to baseline

时间窗: Day 56

次要结局

  • Change in Ca x P product at Day 56 compared to baseline(Day 56)
  • Change in serum phosphorus at Day 28 as compared to baseline(Day 28)
  • Change in Ca x P product at Day 28 compared to baseline(Day 28)
  • Cumulative drop out rate due to serum phosphorus concentration >9mg/dL at Day 56(Day 56)
  • Cumulative drop out rate due to serum Phosphorus concentration >9mg/dL at Day 28(Day 28)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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