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临床试验/JPRN-jRCT2080223803
JPRN-jRCT2080223803尚未招募1 期

Pharmacokinetics and Glucodynamics of LY900014 Compared to Insulin Lispro (Humalog) Following Single Dose Administration in Japanese Patients With Type 1 Diabetes Mellitus

Eli Lilly Japan K.K.0 个研究点开始时间: 2018年2月8日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募

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
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • Inclusion Criteria:
  • - Are Japanese male or female participant with a diagnosis of T1DM
  • - Have a body mass index (BMI) of 18.5 to 30.0 kilograms per square meter (kg/m2)
  • - Have a glycated hemoglobin <9.0%

排除标准

  • - Are receiving chronic systemic or inhaled glucocorticoid therapy, or have received such therapy before screening
  • - Have a history of renal impairment, or have a high serum creatinine level
  • - Have proliferative retinopathy or maculopathy and/or severe neuropathy; in particular, autonomic neuropathy based onophthalmologic examination
  • - Have had any significant changes in insulin regimen and/or unstable blood glucose control prior to screening
  • - Require daily insulin treatment >1.5 units per kilogram (U/kg)

研究者

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