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临床试验/NCT03353350
NCT03353350已完成3 期

A 56-week, Multicenter, Double-blind, Placebo-controlled, Randomized Study to Evaluate the Efficacy and Safety of Efpeglenatide Once Weekly in Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Diet and Exercise

Hanmi Pharmaceutical Company Limited54 个研究点 分布在 5 个国家目标入组 406 人开始时间: 2017年12月5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
发起方
入组人数
406
试验地点
54
主要终点
Change in Glycated Hemoglobin (HbA1c) (%)

研究概览

简要总结

Primary Objective:

To demonstrate the superiority of once weekly injection of efpeglenatide in comparison to placebo in glycated hemoglobin (HbA1c) change in participants with T2DM (Type 2 Diabetes Mellitus) inadequately controlled with diet and exercise.

Secondary Objectives:

  • To demonstrate the superiority of once-weekly injection of efpeglenatide in comparison to placebo on glycemic control
  • To demonstrate the superiority of once-weekly injection of efpeglenatide in comparison to placebo on body weight
  • To evaluate the safety of once-weekly injection of efpeglenatide

详细描述

Study duration per participant is approximately 65 weeks, including a 3-week screening period, 30 weeks core treatment period, 26 weeks extension treatment period, and 6 weeks safety follow up.

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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Efpeglenatide 2mg

Experimental

Efpeglenatide low dose (Prefilled syringe) administered once weekly for 56 weeks

干预措施: efpeglenatide (SAR439977) (Drug)

Efpeglenatide 4 mg

Experimental

Efpeglenatide middle dose (Prefilled syringe) administered once weekly for 56 weeks (including titration period)

干预措施: efpeglenatide (SAR439977) (Drug)

Efpeglenatide 6 mg

Experimental

Efpeglenatide high dose (Prefilled syringe) administered once weekly for 56 weeks (including titration period)

干预措施: efpeglenatide (SAR439977) (Drug)

Placebo

Placebo Comparator

Matching placebo (Prefilled syringe) administered once weekly for 56 weeks

干预措施: placebo (Drug)

结局指标

主要结局

Change in Glycated Hemoglobin (HbA1c) (%)

时间窗: Baseline to Week 30

Change from Baseline to Week 30 in HbA1c

次要结局

  • Hypoglycemic Events(Baseline to Week 56)
  • Change in Body Weight at Week 56(Baseline to Week 56)
  • Change in HbA1c (%)(Baseline to Week 56)
  • HbA1c <7%(Week 30)
  • Change in Body Weight at Week 30(Baseline to Week 30)
  • Hypoglycemic Participants(Baseline to Week 56)
  • Change in Fasting Plasma Glucose (FPG)(Baseline to Week 30)
  • Treatment Emergent Adverse Events (TEAEs)(Baseline to Week 56)

研究者

发起方
Hanmi Pharmaceutical Company Limited
申办方类型
Industry
责任方
Sponsor

研究点 (54)

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