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临床试验/NCT00892749
NCT00892749已完成3 期

A Phase 3, Long-term Study in Patients With Chronic Kidney Disease (CKD) and Hyperphosphatemia on Hemodialysis

Astellas Pharma Inc0 个研究点目标入组 248 人开始时间: 2009年5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
248
主要终点
Changes in serum Phosphorus level

研究概览

简要总结

This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 for long-term dosing in chronic kidney disease and hyperphosphatemia patients on hemodialysis.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Chronic kidney disease patients on hemodialysis
  • Hyperphosphatemia
  • Written informed consent

排除标准

  • Patients with gastrointestinal surgery or enterectomy
  • Severe cardiac disease patients
  • Patients with severe constipation or diarrhea
  • Patients with a complication of malignant tumors
  • Patients with uncontrolled hypertension
  • Patients treated with parathyroid intervention

研究组 & 干预措施

1. ASP1585

Experimental

干预措施: ASP1585 (Drug)

结局指标

主要结局

Changes in serum Phosphorus level

时间窗: After 48 weeks

次要结局

  • Changes in intact PTH level(After 48 weeks)
  • Percent of the patients meeting the target range of serum Phosphorus levels(During the treatment)
  • Changes in serum Calcium level(After 48 weeks)
  • Changes in serum Ca x P(After 48 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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