EUCTR2007-005317-19-ES进行中（未招募）1 期
Efecto de insulina detemir en combinación con liraglutida y metformina en comparación con liraglutida y metformina en sujetos con diabetes tipo 2. Ensayo de 26 semanas, aleatorizado, abierto, de grupos paralelos, multicéntrico, multinacional con una extensión de 26 semanas
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
- 940
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
- •1. Informed consent obtained before any trial-related activities (trial-related activities are any procedure that would not have been performed during normal management of the subject)
- •2. Subjects diagnosed with type 2 diabetes, insulin naïve and treated with metformin as monotherapy for ? 3 months prior to screening, at a stable dose of ? 1500 mg/day or metformin (? 1500 mg/day) and a sulfonylurea (less than or equal to ½ of the maximum approved dose according to local label), both at a stable dose for ? 3 months prior to screening. Previous short-term insulin treatment in connection with intercurrent illness is allowed, at the discretion of the Investigator.
- •3. HbA1c 7.0-10.0% (both inclusive) for subjects on metformin monotherapy
- •HbA1c 7.0-8.5% (both inclusive) for subjects on metformin with a sulfonylurea
- •4. Age 18-80 years, both inclusive (or as allowed according to local guidelines)
- •5. Able and willing to perform self-monitoring of plasma glucose according to the protocol, to keep a diabetes diary and willing to use pen-injector device and FlexPen® device if necessary
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Previous treatment with insulin (except for short-term treatment in connection with intercurrent illness at the discretion of the Investigator)
- •2. Treatment with glucose-lowering agent(s) other than stated in the inclusion criteria in a period of 3 months prior to screening
- •3. Impaired liver function, defined as alanine aminotransferase (ALAT) ? 2.5 times upper normal limit (one retest analysed at the central laboratory within a week is permitted with the result of the last sample being the conclusive)
- •4. Impaired renal function defined as serum-creatinine ? 133 µmol/L (? 1.5 mg/dL) for males and ? 115 µmol/L (? 1.4 mg/dL) for females, or as allowed according to local contraindications for metformin or sulfonylurea use (one retest analysed at the central laboratory within a week permitted with the result of the last sample being the conclusive)
- •5. History of chronic pancreatitis or idiopathic acute pancreatitis
- •6. Known history of unstable angina, acute coronary event, other significant cardiac event (including history of arrhythmias or conduction delays on ECG), or cerebral stroke within the past 6 months.
- •7. Heart failure NYHA class IV (see appendix D)
- •8. Known proliferative retinopathy or maculopathy requiring acute treatment as judged by the Investigator
- •9. Uncontrolled treated or untreated hypertension (systolic blood pressure ? 180 mmHg and/or diastolic blood pressure ? 110 mmHg)
- •10. Cancer (except basal cell skin cancer or squamous cell skin cancer) or any clinically significant disorder, except for conditions associated with type 2 diabetes history which in the Investigator?s opinion could interfere with the results of the trial
- •11. Recurrent major hypoglycaemia or hypoglycaemic unawareness as judged by the Investigator
- •12. Known or suspected allergy to trial product(s) or related products
- •13. Use of any drug (except for those stated in the inclusion criteria), which in the Investigator?s opinion could interfere with the glucose level (eg systemic corticosteroids)
- •14. Receipt of any other investigational drug within 3 months prior to screening into this trial
- •15. Any contraindications to metformin or insulin detemir according to the local label
- •16. Surgery scheduled for the trial duration period (excluding minor surgical procedures performed in local anaesthesia, as judged by the Investigator)
- •17. Previous participation in the run-in period of this trial.
- •18. Known or suspected abuse of alcohol or narcotics
- •19. Females of child bearing potential who are pregnant, breast-feeding or intend to become pregnant or are not using adequate contraceptive methods (adequate contraceptive measures as required by local law or practice) UK: Adequate contraceptive measures are defined as established use of oral, injected or implanted hormonal methods of contraception, sterilisation, intrauterine device or intrauterine system, or consistent use of barrier methods. France: Adequate contraceptive measures are defined as oral hormonal method of contraception or intrauterine device. Germany: Adequate contraceptive measures are implants, injectables, combined oral contraceptives, hormonal IUD, sexual abstinence or vasectomised partner.
- •20. Mental incapacity, unwillingness or language barrier precluding adequate understanding or cooperation
- •21. Subjects with medical history of MEN2 or FMTC if total thyroidectomy has not been performed or cannot be ensured (i.e. posterior capsule of the thyroid gland not removed)
研究者
相似试验
进行中（未招募）
1 期
The effect of insulin detemir in combination with liraglutide and metformin compared to liraglutide and metformin in subjects with type 2 diabetes. A 26-week, randomised, open-label, parallel-group, multicentre, multinational trial with a 26-week extensioType 2 diabetesMedDRA version: 9.1 Level: LLT Classification code 10045242 Term: Type II diabetes mellitusEUCTR2007-005317-19-GBovo Nordisk A/S940
进行中（未招募）
不适用
The effect of insulin detemir in combination with liraglutide and metformin compared to liraglutide and metformin in subjects with type 2 diabetes. A 26-week, randomised, open-label, parallel-group, multicentre, multinational trial with a 26-week extension - NDEUCTR2007-005317-19-ITOVO NORDISK940
进行中（未招募）
1 期
The effect of insulin detemir in combination with liraglutide and metformin compared to liraglutide and metformin in subjects with type 2 diabetes.A 26-week, randomised, open-label, parallel-group, multicentre, multinational trial with a 26-week extensioEUCTR2007-005317-19-FRovo Nordisk A/S940
进行中（未招募）
不适用
The effect of insulin detemir in combination with liraglutide and metformin compared to liraglutide and metformin in subjects with type 2 diabetes.A 26-week, randomised, open-label, parallel-group, multicentre, multinational trial with a 26-week extensioEUCTR2007-005317-19-BEovo Nordisk A/S940
进行中（未招募）
不适用
The effect of insulin detemir in combination with liraglutide and metformin compared to liraglutide and metformin in subjects with type 2 diabetes.A 26-week, randomised, open-label, parallel-group, multicentre, multinational trial with a 26-week extensioEUCTR2007-005317-19-DEovo Nordisk A/S940