CTRI/2009/091/000119已完成3 期
A Randomized, Double-Blind, Placebo-Controlled Parallel Group Efficacy and Safety Study of BI 1356 (5 mg Administered Orally Once Daily) Over 18 Weeks in Type 2 Diabetic Patients With Insufficient Glycaemic Control (HbA1c 7.0-10%) Despite Background Therapy With a Sulfonylurea Drug.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 255
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Patients between 18 and 80 years old with type 2 diabetes and insufficient glycemic control (HbA1c 7% to 10%) despite therapy with a sulfonylurea drug
- •Age minimum: 18 Years
- •Age maximum: 80 Years
- •Gender: Both
排除标准
- •Myocardial infarction,stroke or transient ischaemic attack in last 6 months - Treatment with rosiglitazone, pioglitazone, GLP-1 analogues, insulin or anti-obesity drugs in the past 3 months - Impaired hepatic function - Severe renal impairment - Current treatment with systemic steroids - Change in thyroid hormone dosage - Hereditary galactose intolerance
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