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临床试验/NCT00497198
NCT00497198已完成2 期

An Exploratory Study of MCI-196 for Treatment of Type 2 Diabetes in Randomized, Double-Blind, Parallel-Assignment, Placebo-Controlled Manner

Tanabe Pharma Corporation0 个研究点目标入组 183 人开始时间: 2005年10月1日最近更新:
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
183
主要终点
Fasting Plasma Glucose at Baseline

研究概览

简要总结

The objective of this study is to evaluate the efficacy of MCI-196 in patients with Type 2 Diabetes based on the changes in blood glucose-related parameters and safety after 12 weeks administration in double-blind, placebo-controlled manner. And in addition, the changes in lipid-related parameters are examined.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • Patients whose fasting blood glucose levels during the observation period are between 130mg/dL and 200mg/dL.
  • Patients whose HbA1c is 7.0% or above during the observation period.

排除标准

  • Patients with serious cardiac, hepatic or renal complications.
  • Patients with serious diabetic complications.
  • Patients with complete biliary obstruction or ileus.
  • Pregnant, lactating, and probably pregnant patients, and patients who can not agree to contraception.

研究组 & 干预措施

MCI-196

Experimental

干预措施: MCI-196 (Drug)

Placebo

Placebo Comparator

干预措施: Placebo of MCI-196 Tablet (Drug)

结局指标

主要结局

Fasting Plasma Glucose at Baseline

时间窗: 0 weeks

Change From Baseline in Blood Glucose at Week 12

时间窗: 12 weeks (baseline to week 12)

Hemoglobin A1c (HbA1c) at Baseline

时间窗: 0 weeks

Change From Baseline in Hemoglobin A1c(HbA1c) at Week 12

时间窗: 12 weeks (baseline to week 12)

次要结局

  • Change From Baseline in Low Density Lipoprotein Cholesterol(LDL-c) at Week 12(12 weeks (baseline to week 12))

研究者

申办方类型
Industry

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