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临床试验/NCT01766778
NCT01766778已完成4 期

A Local Phase IV, Multicenter, Open-label Study to Evaluate Early add-on Vildagliptin in Patients With Type 2 Diabetes Inadequately Controlled by Metformin

Novartis Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 117 人开始时间: 2013年5月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
117
试验地点
1
主要终点
Change of Glycosylated Hemoglobin A1c (HbA1c) From Baseline to Month 12

研究概览

简要总结

The purpose of this study was to observe change of HbA1c over time from baseline to month 12. The ultimate goal of this study was to provide a local reference value to the physicians & patients in the future when they consider initiating Vildagliptin and taking balance between efficacy, compliance, risk factors, convenience and medication cost.

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
None

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

  • Male or Female in age ≥18 at Visit 1
  • Type 2 diabetes mellitus (T2DM) patients on their maximum tolerated dose of Metformin for more than 3 months
  • HbA1c (glycosylated hemoglobin) at Visit 1 greater than 7.0%
  • With nearest documented record of HbA1c before Visit 1 greater than 7.0% after patient reached his/her maximum tolerated dose of Metformin

排除标准

  • Patients with hepatic impairment, including patients with a pre-treatment alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 X the upper limit of normal at Visit 1
  • Patients with moderate or severe renal impairment or end-stage-renal-disease (ESRD) on haemodialysis at the time of enrolment
  • Patients with hereditary problems of galactose intolerance, the Lapp lactose deficiency or glucose-galactose malabsorption
  • Pregnant women or breastfeeding women at the time of enrolment
  • Use of insulin or other oral anti-diabetic drug (OAD) apart from Metformin in the past for T2DM treatment

研究组 & 干预措施

LAF237 (vildagliptin) 50mg once daily (QD)

Active Comparator

Vildagliptin 50mg QD plus stabilized or maximum tolerated dose of Metformin

干预措施: LAF237 (vildagliptin) (Drug)

LAF237 (vildagliptin) 50mg once daily (QD)

Active Comparator

Vildagliptin 50mg QD plus stabilized or maximum tolerated dose of Metformin

干预措施: Metformin (Drug)

LAF237 (vildagliptin) 50mg twice daily (BID)

Active Comparator

Vildagliptin 50mg BID plus stabilized or maximum tolerated dose of Metformin

干预措施: LAF237 (vildagliptin) (Drug)

LAF237 (vildagliptin) 50mg twice daily (BID)

Active Comparator

Vildagliptin 50mg BID plus stabilized or maximum tolerated dose of Metformin

干预措施: Metformin (Drug)

结局指标

主要结局

Change of Glycosylated Hemoglobin A1c (HbA1c) From Baseline to Month 12

时间窗: Baseline, Month 12 (weeK 52)

HbA1c is an integrated measure of average glucose concentration in plasma in the last 2-3 months. Blood samples were collected to analyze HbA1c

次要结局

  • Change of Glycosylated Hemoglobin A1c (HbA1c) From Baseline to Month 3, 6, 9 and 12 (Based on MMRM Analysis)(Baseline, Month 3, 6, 9 and 12)
  • Change in Fasting Plasma Glucose (FPG) From Baseline to Month 3, 6, 9 and 12 (Based on MMRM Analysis)(Baseline, Month 3, 6, 9 and 12)
  • Percentage of Patients Achieving Good Glycemic Control(Month 3, 6, 9, 12)
  • Percentage of Overall Drug Compliance in 12 Months(Month 12)
  • Number of Patients With Adverse Events, Serious Adverse Events and Death as an Assessment of Overall Safety and Tolerability(Month 12)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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