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临床试验/JPRN-jRCT2080220603
JPRN-jRCT2080220603未知2 期

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

Takeda Pharmaceutical Company Limited0 个研究点目标入组 240 人开始时间: 2008年9月5日最近更新:
适应症

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 sulfonylurea for at least 4 weeks prior to the initiation of the observation period.
  • The subject has been taking sulfonylurea at a stable dose regimen for at least 12 weeks prior to the initiation of the treatment period(Week 0).
  • The subject has an HbA1C of 7.0% or more and below 10.0% at 8 weeks after the initiation of the observation period(Week -4).

排除标准

  • Key Criteria for exclusion:
  • The subject has taken other diabetic medications than sulfonylurea within 12 weeks before the initiation of the treatment period (Week 0).

研究者

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