跳至主要内容
临床试验/JPRN-jRCT2080220568
JPRN-jRCT2080220568未知2 期

A Phase 2/3 Study of SYR-322 as an Add-on to a Thiazolidine

Takeda Pharmaceutical Company Limited0 个研究点目标入组 240 人开始时间: 2008年6月10日最近更新:

试验速览

阶段
2 期
入组人数
240

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • Key Criteria for inclusion:
  • - The subject has been taking a stable dosage regimen of pioglitazone for at least 16 weeks prior to the initiation of the treatment period (Week 0)
  • - The subject has an HbA1c value of 6.5% or more and below 10.0% at 14 weeks after the initiation of the screening period (Week -2)
  • Key Criteria for exclusion:
  • - The subject has taken any antidiabetic medications except pioglitazone within the last 16 weeks prior to the initiation of the treatment period (Week 0)
  • - The subject with a history or symptoms of heart failure

排除标准

  • 未提供

研究者

相似试验