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临床试验/NCT01413204
NCT01413204已完成3 期

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of TA-7284 as Monotherapy in the Treatment of Subjects With Type 2 Diabetes Mellitus

Tanabe Pharma Corporation5 个研究点 分布在 1 个国家目标入组 272 人开始时间: 2011年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
272
试验地点
5
主要终点
Change in Hemoglobin A1c (A1C) From Baseline (NGSP Value)

研究概览

简要总结

The purpose of this study is to evaluate the efficacy and safety of TA-7284 as monotherapy in patients with type 2 Diabetes for 24 weeks administration.

详细描述

This is a randomized, 3-arm, parallel group, double blind study to evaluate the efficacy and safety of TA-7284 in Japanese patients with Type 2 diabetes mellitus, who are not optimally controlled on diet and exercise. The patients will receive either TA-7284-Low, TA-7284-High or Placebo orally alone for 24 weeks.

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
Triple (Participant, Care Provider, Investigator)

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

  • Men or women age ≥20 years old
  • Diagnosed with Type 2 diabetes mellitus at least 3 months before run-in period
  • HbA1c of ≥7.0% and ≤10.0%

排除标准

  • Type I diabetes mellitus, diabetes mellitus resulting from pancreatic disorder, secondary diabetes mellitus
  • Past or current history of severe diabetic complications
  • Fasting plasma glucose > 270 mg/dL before treatment start
  • History of hereditary glucose-galactose malabsorption or primary renal glucosuria
  • Patients requiring insulin therapy

研究组 & 干预措施

TA-7284 Low

Experimental

干预措施: TA-7284 Low (Drug)

TA-7284 High

Experimental

干预措施: TA-7284 High (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Change in Hemoglobin A1c (A1C) From Baseline (NGSP Value)

时间窗: baseline and 24 weeks

次要结局

  • Change in Fasting Plasma Glucose(Week 24)
  • Change in Body Weight(Week 24)
  • Change in Blood Pressure(Week 24)
  • Safety and Tolerability Assessed by Adverse Events, Hypoglycemic Events, Laboratory Tests, 12-lead ECG and Vital Signs(Week 24)
  • Change in Postprandial Plasma Glucose, Insulin and Urinary Glucose Excretion After a 75 g Oral Glucose Tolerance Test(Week 24)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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