CTRI/2009/091/000091已完成2 期
A 12-Week,Double-Blind, Placebo-Controlled Trial of LY2428757 in Patients With Type 2 Diabetes Mellitus
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- Eli Lilly
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
- •Have type 2 diabetes mellitus for at least 6 months prior to entering the trial.
- •-Treated with diet and exercise alone or in combination with at least 1000 mg/day of metformin for at least 2 months prior to screening.
- •-Have an HbA1c value of 7.0% - 10.0% at screening
- •-Women of child-bearing potential must test negative for pregnancy at screening and agree to abstain from heterosexual intercourse for the duration of the study, or use 2 effective forms of birth control during the study.
- •-Have a body mass index (BMI) between 25 and 40 kg/m2 at screening
- •-Stable weight during the 3 months prior to screening.
排除标准
- •-Use any antidiabetic agent other than metformin during the 2 months prior to screening.
- •-Have a gastrointestinal disease that significantly impacts gastric emptying or motility or have undergone bariatric surgery.
- •-Are currently taking prescription or over-the counter medications to promote weight loss.
- •-Have been previously diagnosed with pancreatitis
- •-Women who are breastfeeding.
- •-Have a history of myocardial infarction, unstable angina, coronary artery bypass graft (CABG), percutaneous coronary intervention, transient ischemic attack, stroke or decompensated congestive heart failure in the past 6 months.
- •-Have poorly controlled hypertension
研究者
相似试验
进行中(未招募)
1 期
A 12-Week, Double-Blind, Placebo-Controlled Trial of LY2428757 in Patients with Type 2 Diabetes MellitusEUCTR2008-004207-63-DEEli Lilly and Company, Indianapolis300
进行中(未招募)
不适用
A 12-Week, Double-Blind, Placebo-Controlled Trial of LY2428757 in Patients with Type 2 Diabetes MellitusEUCTR2008-004207-63-GBEli Lilly and Company, Indianapolis300
进行中(未招募)
不适用
A 12-Week, Double-Blind, Placebo-Controlled Trial of LY2428757 in Patients with Type 2 Diabetes MellitusEUCTR2008-004207-63-ATEli Lilly and Company, Indianapolis300
已完成
不适用
A 12-Week, Randomized, Double-blind, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of FerShizn on Improving Body Fat of Overweight or Obesity Subject.Endocrine, nutritional and metabolic diseasesKCT0007809utracore100
尚未招募
不适用
a clinical trial to effect of oral lacto-bacteria for the improvement of periodontal diseaseKCT0006582DENTIS63
