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临床试验/DRKS00010275
DRKS00010275招募中1 期

A Phase 1/2, Randomized, Double-blind,Placebo-controlled, Multiple-ascending-dose Studyto Evaluate the Efficacy, Safety, and Pharmacokineticsof MEDI0382 in Overweight and Obese Subjectswith a History of Type 2 Diabetes Mellitus - MEDI0382 MAD

MedImmune Limited, a wholly owned subsidiary of AstraZeneca PLC0 个研究点目标入组 107 人开始时间: 2016年4月25日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
107

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • The study population will consist of male or female adults, 18 through 65 years of age with T2DM and body mass index 27 to 40 kg/m2 (inclusive), without significant late diabetic complications. Subjects should have been treated with a stable dose of oral blood glucose lowering therapy for 3 months prior to screening (metformin monotherapy or metformin plus dipeptidyl peptidase-4 [DPPIV], sulphonylurea [50% of the licensed dose], or a sodium-glucose co-transporter 2 [SGLT2]; and DPPIV inhibitor, sulphonylurea, or SGLT2 inhibitor is washed out prior to randomization).

排除标准

  • Females of childbearing potential and lactating females will be excluded.

研究者

发起方
MedImmune Limited, a wholly owned subsidiary of AstraZeneca PLC

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