EUCTR2015-005356-99-GR进行中（未招募）1 期
A Prospective, Randomized, Double-Blind Comparison of LY900014 to Insulin Lispro with an Open-Label Postprandial LY900014 Treatment Group, in Combination with Insulin Glargine or Insulin Degludec, in Adults with Type 1 Diabetes. PRONTO-T1D - PRONTO-T1D
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 1,199
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •You were diagnosed with type 1 diabetes at least one year ago.
- •You are 18 years old or older.
- •You are already using a long-acting insulin and rapid-acting insulin analog.
- •Your blood glucose levels are within allowed limits for study participation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 899
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 300
排除标准
- •You have had more than 1 emergency treatment for very low blood glucose in the last 6 months.
- •You have had more than 1 emergency treatment for poor glucose control in the last 6 months.
- •You are taking certain diabetes medications that are not allowed for study participation.
- •You have major problems with your heart, kidneys, liver, or you have a blood disorder.
- •You have had or are now being treated for certain types of cancer that prevents you from study participation.
研究者
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不适用
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