跳至主要内容
临床试验/NCT00995618
NCT00995618已完成2 期

A Randomized, Double-Blind, Crossover, Pharmacodynamic and Pharmacokinetic Drug Interaction Study of Tranilast in Combination With Febuxostat Compared With Tranilast Alone and Febuxostat Alone in Healthy Subjects With Hyperuricemia

Nuon Therapeutics, Inc.1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2009年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
24
试验地点
1
主要终点
Mean decrease in serum uric acid levels

研究概览

简要总结

This is a randomized, double-blind, 3-period crossover phase 2 study in patients with documented hyperuricemia to evaluate the effect of tranilast on febuxostat pharmacokinetics (PK) and pharmacodynamics (PD) and to evaluate the effect of febuxostat on tranilast PK and PD as measured by reduction in serum uric acid levels.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female, aged 18 to 70
  • Subjects with hyperuricemia who are otherwise healthy

排除标准

  • Pregnant or nursing
  • Known history of gout
  • Clinically significant infection at Screening
  • Known sensitivity to tranilast or febuxostat

研究组 & 干预措施

Tranilast

Experimental

Tranilast tablets

干预措施: Tranilast (Drug)

Febuxostat

Active Comparator

Febuxostat tablets

干预措施: Febuxostat (Drug)

Combination

Experimental

Tranilast plus febuxostat

干预措施: Combination - Tranilast and Febuxostat (Drug)

结局指标

主要结局

Mean decrease in serum uric acid levels

时间窗: Seven days

次要结局

  • Analysis of pharmacokinetic parameters (AUC, Cmax) of tranilast, febuxostat and combination(7 days)

研究者

申办方类型
Industry

研究点 (1)

Loading locations...

相似试验

Study of Tranilast Alone or in Combination With... | 临床试验