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临床试验/JPRN-UMIN000002840
JPRN-UMIN000002840已完成未知

Multicenter, randomized, placebo- controlled, double blind study of HS219 to evaluate the efficacy and safety in chronic kidney disease patients on hemodialysis with hyperphosphatemia - Study of HS219 in chronic kidney disease patients on hemodialysis with hyperphosphatemia

Healthserve0 个研究点目标入组 64 人开始时间: 2009年12月7日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
64

研究概览

简要总结

Sixty eight HD patients maintained on calcium carbonate (33 subjects) or sevelamer (35 subjects) were enrolled during January - April, 2010. Sixty-three patients chewed at least one gum: 35 HS219 and 28 placebo. HS219 was well tolerated and safe. However, no significant effect of HS219 on reduction of serum phosphorous was observed. There were no significant differences between HS219 and placebo in the ratio of 1.5 mg/dL of reduction of serum phosphorus level and the rate of achievement to the targeted serum phosphorus level; &#8805; 3.5 mg/dL and < 5.5 mg/dL. There were no significant effects of HS219 on change of salivary phosphorus, serum Ca, serum Ca x P, iPTH and EGF 23.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Blood purification therapy other than hemodialysis 2. Current clinically significant intestinal motility disorder 3. Possible parathyroid intervention during the study period 4. History of malignancy and severe cardiovascular disorders such as heart disease, angina, congested heart failure, valve stenosis, atrial fibrillation and arrhythmia 5. Receipt of any investigational drug within 30 days of informed consent

研究者

发起方
Healthserve

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