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临床试验/JPRN-jRCT2080221729
JPRN-jRCT2080221729未知1 期

A Randomized, Placebo-Controlled, Double-Blinded, Multiple Dose Escalation Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of BMS-823778 in Healthy Subjects and Patients with Type 2 Diabetes Mellitus

Bristol-Myers K.K.0 个研究点目标入组 40 人开始时间: 2012年3月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
40

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 <= 65age old(—)
性别
All

入选标准

  • for T2DM patients:
  • - Japanese patients with Type 2 Diabetes Mellitus (Fasting glucose < 240 mg/dL, HbA1c: 6.5% to 10.0% (NGSP)) who are treatment-naive and managed with diet and/or exercises only.

排除标准

  • for T2DM patients:
  • - Patient who is taking any medication for T2DM
  • - Symptoms of poorly controlled diabetes that would preclude participation in this placebo-controlled trial
  • - Insulin therapy within one year of screening

研究者

发起方
Bristol-Myers K.K.

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