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临床试验/NCT01968044
NCT01968044已完成3 期

A Multicenter,Randomized, Placebo-controlled, Parallel Group, Double-blind, Phase IIIb Study to Evaluate the Safety and Efficacy After 12 Weeks Administration of Gemigliptin and Placebo in Type 2 Diabetes Mellitus Patients With Moderate or Severe Renal Impairment With an Additional 40 Weeks, Double-blind,Active-controlled, Double-dummy,Long-term Extension Study

LG Life Sciences0 个研究点目标入组 132 人开始时间: 2013年10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
发起方
入组人数
132
主要终点
HbA1c change

研究概览

简要总结

Therapuetic options are limited for Type 2 Diabetes Mellitus (T2DM) pateints with renal impairment. This clinical study is to asses safety and efficacy of the DPP-4 inhibitor gemigliptin in patients with type 2 DM and moderate or severe renal impairment for long-term peirod (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
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with Type 2 Diabetes Mellitus
  • Patients with moderate or severe renal insufficiency
  • All patients give written informed consent

排除标准

  • Has type 1 diabetes mellitus or a history of ketoacidosis
  • Is on dialysis or is likely to need dialysis during the study
  • Has active liver disease

研究组 & 干预措施

Gemigliptin

Experimental

Participant will remain gemigliptin 50mg throughout entire study (52 weeks).

干预措施: Gemigliptin (Drug)

Placebo to linagliptin

Other

Participant who is randomized to placebo will be switched to linagliptin after 12 week and administered linagliptin by week 52.

干预措施: Placebo to Linagliptin (Drug)

结局指标

主要结局

HbA1c change

时间窗: HbA1c change from baseline to week 12

次要结局

  • HbA1c Change(HbA1c change from baselint to week 6, 52)
  • FPG(FPG change from baseline to week 6,12,52)
  • Glycated albumin(Glycated albumin change from baseline to week 6,12,52)
  • Fructosamin(Fructosamin change from baseline to week 6,12,52)
  • Waist(Waist change from baseline to week 12,52)
  • HbA1c responser (HbA1c<7.0%)(HbA1c responser rate at week 12,52)
  • Fasting serum C-peptide(Fasting serum C-peptide change from baseline to week 12,52)
  • Fasting Lipid parameters(Fasting Lipid parameters change from baseline to week 12,52)
  • Albuminuria(Albuminuria change from baseline to week 12,52)

研究者

发起方
LG Life Sciences
申办方类型
Industry
责任方
Sponsor

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