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临床试验/NCT00138554
NCT00138554已完成3 期

Extension to a Study on the Efficacy and Safety of Vildagliptin in Combination With Pioglitazone in Patients With Type 2 Diabetes

Novartis1 个研究点 分布在 1 个国家目标入组 318 人开始时间: 2004年11月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
Novartis
入组人数
318
试验地点
1
主要终点
Safety of vildagliptin in combination with pioglitazone during 52 weeks of treatment

研究概览

简要总结

Many people with type 2 diabetes cannot maintain target blood glucose levels when taking a single oral drug. This is a 28-week extension to a study to assess the safety and effectiveness of vildagliptin, an unapproved drug, in lowering overall blood glucose levels when added to pioglitazone in people with type 2 diabetes not at target blood glucose levels on pioglitazone or rosiglitazone alone. The purpose of the extension study is to gather data on the long-term safety and effectiveness of vildagliptin in people with type 2 diabetes.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Only patients successfully completing study CLAF237A2304 are eligible
  • Written informed consent
  • Ability to comply with all study requirements

排除标准

  • Premature discontinuation from study CLAF237A2304
  • Other protocol-defined exclusion criteria may apply

研究组 & 干预措施

vildagliptin 50 mg qd + pioglitazone 45 mg qd

Experimental

vildagliptin 50 mg qd + pioglitazone 45 mg qd for 28 weeks

干预措施: vildagliptin (Drug)

vildagliptin 50 mg qd + pioglitazone 45 mg qd

Experimental

vildagliptin 50 mg qd + pioglitazone 45 mg qd for 28 weeks

干预措施: pioglitazone (Drug)

vildagliptin 50 mg bd+ pioglitazone 45 mg qd

Experimental

vildagliptin 50 mg bd + pioglitazone 45 mg qd for 28 weeks

干预措施: vildagliptin (Drug)

vildagliptin 50 mg bd+ pioglitazone 45 mg qd

Experimental

vildagliptin 50 mg bd + pioglitazone 45 mg qd for 28 weeks

干预措施: pioglitazone (Drug)

结局指标

主要结局

Safety of vildagliptin in combination with pioglitazone during 52 weeks of treatment

Change from baseline in HbA1c at 52 weeks

次要结局

  • Change from baseline in HOMA IR at 52 weeks
  • Change from baseline in HOMA B at 52 weeks
  • Change in HbA1c between 24 weeks and 52 weeks
  • Change from baseline in fasting plasma glucose at 52 weeks
  • Change in fasting plasma glucose between 24 weeks and 52 weeks

研究者

发起方
Novartis
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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