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临床试验/NCT02367066
NCT02367066已完成1 期

A Single Centre, Double-blind, Randomised, Placebo-controlled, Cross-over Phase I Study to Assess the Pharmacodynamics of Oral AR-C165395XX After Administration of Repeated Doses for 3 Days in Subjects With Type 2 Diabetes Mellitus

AstraZeneca1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
AstraZeneca
入组人数
30
试验地点
1
主要终点
Change From Baseline to Endpoint MMTT AUC(0-4h) for Plasma Glucose

研究概览

简要总结

A study to assess the Pharmacodynamics of oral AR-C165395XX after Administration of Repeated Doses for 3 days in Subjects with Type 2 Diabetes Mellitus

详细描述

A Single Centre, Double-blind, Randomised, Placebo-controlled, Cross-over Phase I Study to Assess the Pharmacodynamics of oral AR-C165395XX after Administration of Repeated Doses for 3 days in Subjects with Type 2 Diabetes Mellitus

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 130 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • History or sign of any clinically significant disease or disorder which, in the opinion f the investigator, may either put the subject at risk because of participation in the sudy, or influence the results or the subject's ability to participate in the study
  • Any clinically significant abnormalities in clinical chemistry, haematology or urinalysis results as judged by the investigator
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) laboratory results >3x upper level of normal range (ULN) Clinical diagnosis of Type 1 diabetes mellitus and/or history of diabetic ketoacidosis or positive Glutamic Acid Decarboxylase Autoantibodies test (GAD antibodies test).
  • Patients treated with single Insulin therapy within the last 3 months

研究组 & 干预措施

AR-C165395XX + placebo

Experimental

1st period AR-C165395XX 2nd period placebo

干预措施: AR-C165395XX (Drug)

Placebo + AR-C165395XX

Placebo Comparator

1st period Placebo for AR-C165395XX 2nd period AR-C165395XX

干预措施: Placebo (Other)

结局指标

主要结局

Change From Baseline to Endpoint MMTT AUC(0-4h) for Plasma Glucose

时间窗: Day -1 to Day 3 and Day 6 to Day 9

MMTT=Mixed Meal Tolerance Test AUC=Area Under Curve

Change From Baseline to Endpoint MMTT C_max for Plasma Glucose

时间窗: Day -1 to Day 3 and Day 6 to Day 9

Change From Baseline to Endpoint GGI AUC(1-2h) for Plasma C-Peptide

时间窗: Day -1 to Day 3 and Day 6 to Day 9

GGI=Glucose and GLP1 infusion AUC=Area Under Curve

次要结局

  • Time of Maximum Plasma AZD1081 Concentration, t_ss,Max(Days 2,3,8,9)
  • Change From Baseline to Endpoint MMTT AUC(0-4h) for Plasma Insulin(Day -1 to Day 3 and Day 6 to Day 9)
  • Plasma AZD1981 AUC(0-1h)(Days 2,3,8,9)
  • Change From Baseline MMTT AUC(0-4h) for Plasma Glucagon(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint MMTT AUC(0-4h) for Plasma C-Peptide(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint GGI AUC(0-1h) for Plasma Insulin(Day -1 to Day 3 and Day 6 to Day 9)
  • Plasma AZD1981 AUC(0-2h)(Days 2,3,8,9)
  • Change From Baseline to Endpoint GGI AUC(1-2h) for Plasma Insulin(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint GGI AUC(0-1h) for Plasma Glucagon(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint GGI AUC(1-2h) for Plasma Glucagon(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint Fasting Beta-cell Responsiveness(Day -1 to Day 3 and Day 6 to Day 9)
  • Fasting Insulin at Endpoint(Day 3 and Day 9)
  • Maximum Plasma AZD1981 Concentration at Steady-State, C_ss,Max(Days 2,3,8,9)
  • Plasma AZD1981 AUC(1-2h)(Days 2,3,8,9)
  • Plasma Paracetamol Maximum Concentration, C_max(Days 3,9)
  • Minimum Plasma AZD1981 Concentration at Steady-State, C_ss,Min(Days 2,3,8,9)
  • Time of Maximum Plasma Paracetamol Concentration, t_max(Days 3,9)
  • Plasma Paracetamol AUC(0-t)(Days 3,9)
  • Change From Baseline to Endpoint GGI AUC(0-1h) for Plasma C-Peptide(Day -1 to Day 3 and Day 6 to Day 9)
  • Change From Baseline to Endpoint GGI AUC(0-24h) for Plasma Glucose(Day -1 to Day 3 and Day 6 to Day 9)
  • Plasma AZD1981 AUC(0-4h)(Days 2,3,8,9)
  • Plasma AZD1981 AUC(0-12h)(Days 2,3,8,9)
  • Plasma AZD1981 AUC(0-24h)(Days 2,3,8,9)
  • Apparent Oral Plasma AZD1981 at Steady-State, CL_ss/F(Days 2,3,8,9)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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