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临床试验/JPRN-jRCT2080223709
JPRN-jRCT2080223709已完成1 期

A Multiple-Ascending Dose Study in Japanese Patients With Type 2 Diabetes Mellitus to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3298176

Eli Lilly Japan K.K.0 个研究点目标入组 49 人开始时间: 2017年11月9日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
49

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

年龄范围
>= 20age old 至 <= 70age old(—)
性别
All

入选标准

  • Have T2DM controlled with diet and exercise alone or are stable on a single oral antidiabetic medication (metformin or dipeptidyl peptidase [DPP]-IV inhibitors)
  • - Have a body mass index of 20.0 to 35.0 kilograms per square meter, inclusive

排除标准

  • - Have known allergies to LY3298176, glucagon-like peptide (GLP)-1 analogs, or related compounds
  • - Have had more than 1 episode of severe hypoglycemia, as defined by the American Diabetes Association criteria, within 6 months before entry into the study or has a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms
  • - Have an abnormality in the 12-lead electrocardiogram at screening that, in the opinion of the investigator, increases the risks associated with participating in the study
  • - Have a history or presence of pancreatitis or gastrointestinal (GI) disorder or any GI disease which impacts gastric emptying or could be aggravated by GLP-1 analogs or DPP-IV inhibitors

研究者

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