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临床试验/NCT02946541
NCT02946541已完成3 期

A Randomized, Double-blind, Placebo-controlled, Phase III Clinical Trial to Investigate the Efficacy and Safety of Evogliptin After Oral Administration in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Diet and Exercise

Dong-A ST Co., Ltd.1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2013年7月最近更新:
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
160
试验地点
1
主要终点
HbA1c

研究概览

简要总结

This is a randomized, double-blind, placebo-controlled, phase III clinical trial to investigate the efficacy and safety of evogliptin after oral administration in patients with type 2 diabetes who have inadequate glycemic control on diet and exercise.

详细描述

  1. Evogliptin 5mg Group: Administration with Evogliptin 5mg for 0-52 weeks.
  2. Placebo Group: Administration with Placebo for 0-24 weeks, and with Evogliptin 5mg for 24-52 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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Subjects with 6.5%≤HbA1c≤10.0% at screening
  • Subjects untreated with oral hypoglycemic agents within 6 weeks prior to screening
  • Subjects with 6.5%≤HbA1c≤10.0% at Visit 2
  • Subjects with 20kg/m2≤BMI≤40kg/m2 at screening

排除标准

  • Subjects with fasting plasma glucose≥270mg/dL at screening
  • Patients with type 1 diabetes mellitus, secondary diabetes mellitus or gestational diabetes mellitus
  • Subjects with history of myocardial infarction, cerebral infarction within 6 months prior to screening
  • Subjects with ALT and AST 2.5 times or higher than upper normal range

研究组 & 干预措施

evogliptin 5mg

Experimental

evogliptin 5mg QD

干预措施: evogliptin 5mg (Drug)

placebo

Placebo Comparator

Placebo QD

干预措施: Placebo (Drug)

结局指标

主要结局

HbA1c

时间窗: Change from baseline at 24 weeks

unit: %

次要结局

  • HbA1c response rate(Change from baseline at 24 weeks)
  • fasting plasma glucose(Change from baseline at 24 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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