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临床试验/EUCTR2014-003621-18-HU
EUCTR2014-003621-18-HU进行中(未招募)1 期

DUAL™VII - Insulin degludec/liraglutide (IDegLira) vs. basal-bolus therapy: A clinical trial comparing efficacy and safety of insulin degludec/liraglutide (IDegLira) versus basal-bolus therapy in subjects with type 2 diabetes mellitus - DUAL™VII

ovo Nordisk A/S0 个研究点目标入组 500 人开始时间: 2015年3月24日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Male or female, age =18 years at the time of signing informed consent
  • - Type 2 diabetes subjects (diagnosed clinically) = 6 months prior to screening
  • - HbA1c 7.0-10.0% [53mmol/mol-86mmol/mol] (both inclusive) by central laboratory analysis
  • - Current treatment with IGlar for at least 90 calendar days prior to screening
  • - Stable daily dose of IGlar between 20 units and 50 units (both inclusive) for at least 56 calendar days prior to screening. Individual fluctuations of ± 10% within the 56 calendar days prior to screening are acceptable, however on the day of screening total daily dose should be within the range of 20 units-50 units both inclusive
  • - Stable daily dose of metformin (=1500 mg or max. tolerated dose) for at least 90 calendar days prior to screening
  • - Body mass index (BMI) = 40 kg/m^2
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 375
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 125

排除标准

  • - Treatment with any medication for the indication of diabetes or obesity other than stated in the inclusion criteria in a period of 90 calendar days before screening
  • - Anticipated initiation or change in concomitant medications in excess of 14 calendar days known to affect weight or glucose metabolism, such as weight loss/modifying (e.g.; sibutramine, orlistat, thyroid hormones, corticosteroids)
  • - Impaired liver function, defined as alanine aminotransferase (ALT) =2.5 times upper limit of normal
  • - Renal impairment eGFR <60 mL/min/1.73 m^2 as per CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration)
  • - Screening calcitonin =50 ng/L
  • - History of pancreatitis (acute or chronic)
  • - Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2

研究者

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