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临床试验/EUCTR2012-000209-63-HU
EUCTR2012-000209-63-HU进行中(未招募)不适用

The efficacy of insulin degludec/liraglutide in controlling glycaemia in adults with type 2 diabetes inadequately controlled on GLP-1 receptor agonist and OAD therapy - DUAL™ III - GLP-1 Switch

ovo Nordisk A/S0 个研究点目标入组 429 人开始时间: 2013年3月14日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
429

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

  • - Subjects with type 2 diabetes mellitus
  • - Male or female = 18 years of age
  • - HbA1c 7.0-9.0% (53-75 mmol/mol) (both inclusive)
  • - Treatment with daily GLP-1 receptor agonist at maximum dose according to local label (i.e. 1.8 mg OD Victoza® (liraglutide) or 10 microgram twice daily (BID) Byetta® (exenatide)) or documented maximum tolerated dose (i.e. 1.2 mg OD Victoza® (liraglutide) or 5 microgram BID Byetta® (exenatide)) in combination with a stable daily dose of metformin (> 1500 mg or documented maximum tolerated dose) ± stable daily dose of pioglitazone (=30 mg) ±stable daily dose of sulphonylurea (= half of the max approved dose according to local label) =90 days prior to screening visit (Visit 1)
  • - BMI (body mass index) = 40 kg/m2
  • 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 321
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 108

排除标准

  • - Any use of oral anti-diabetic drugs (OADs) (except for metformin, pioglitazone and sulphonylurea) = 90 days prior to screening visit (Visit 1)
  • - Use of any drug (except metformin, pioglitazone, sulphonylurea and GLP-1 receptor agonist) which in the Investigators opinion could interfere with the blood glucose level (e.g. systemic corticosteroids)
  • - Treatment with any insulin regimen (short term treatment due to intercurrent illness including gestational diabetes is allowed at the discretion of the Investigator)
  • - Screening calcitonin = 50 ng/l
  • - Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2)
  • - Cardiovascular disorders defined as: congestive heart failure (New York Heart Association (NYHA) class III-IV), diagnosis of unstable angina pectoris, cerebral stroke and/or myocardial infarction within the past 52 weeks prior to screening visit (Visit 1) and/or planned coronary, carotid or peripheral artery revascularisation procedures
  • - Proliferative retinopathy requiring acute treatment or maculopathy (macular oedema) according to the Investigator’s opinion
  • - Subjects with a clinical significant, active (during the past 12 months) disease of the gastrointestinal, pulmonary, endocrinological (except for the type 2 diabetes mellitus), neurological, genitourinary or haematological system that in the opinion of the Investigator may confound the results of the trial or pose additional risk in administering trial products
  • - History of chronic pancreatitis or idiopathic acute pancreatitis

研究者

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