EUCTR2015-001351-71-GB进行中(未招募)1 期
Efficacy and long-term safety of oral semaglutide versus sitagliptin in subjects with type 2 diabetes - PIONEER 3
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
- 1,863
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
入选标准
- •1. Male or female, age = 18 years at the time of signing informed consent.
- •For Japan only: Male or female, age = 20 years at the time of signing informed consent.
- •2. Diagnosed with T2DM = 90 days prior to day of screening.
- •3. HbA1c 7.0-10.5 % (53-91 mmol/mol) (both inclusive).
- •4. Stable daily dose of metformin (= 1500 mg or maximum tolerated dose as documented in subject medical record) alone or in combination with SU (= half of the maximum approved dose according to local label or maximum tolerated dose as documented in subject medical record) within 90 days prior to the day of screening.
- •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 1395
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 465
排除标准
- •1. Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive methods (adequate contraceptive measures as required by local regulation or practice).
- •For certain specific countries: Additional specific requirements apply.
- •2. Family or personal history of Multiple Endocrine Neoplasia Type 2 (MEN 2) or Medullary Thyroid Carcinoma (MTC).
- •3. History of pancreatitis (acute or chronic).
- •4. History of major surgical procedures involving the stomach potentially affecting absorption of trial product (e.g. subtotal and total gastrectomy, sleeve gastrectomy, gastric bypass surgery).
- •5. Any of the following: myocardial infarction, stroke or hospitalization for unstable angina and/or transient ischaemic attack within the past 180 days prior to the day of screening.
- •6. Subjects presently classified as being in New York Heart Association (NYHA) Class IV.
- •7. Planned coronary, carotid or peripheral artery revascularisation known on the day of screening.
- •8. Renal impairment defined as estimated Glomerular Filtration Rate (eGFR) < 60 mL/min/1.73 m^2 as per Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI).
- •9. History or presence of malignant neoplasms within the last 5 years (except basal and squamous cell skin cancer and in-situ carcinomas).
研究者
相似试验
Unknown
3 期
This trial is to see Efficacy and long-term safety of oral semaglutide versus sitagliptin in subjects with type 2 diabetesCTRI/2018/02/011670ovo Nordisk AS
进行中(未招募)
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Efficacy and long-term safety of oral semaglutide versus sitagliptin in subjects with type 2 diabetesMedDRA version: 20.1Level: LLTClassification code 10045242Term: Type II diabetes mellitusSystem Organ Class: 100000004861Diabetes Mellitus, Type 2EUCTR2015-001351-71-DEovo Nordisk A/S1,863
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Research study to compare three doses of semaglutide tablets taken once daily in people with type 2 diabetesDiabetes Mellitus, Type 2EUCTR2020-000299-39-HRovo Nordisk A/S1,224
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Research study to compare three doses of semaglutide tablets taken once daily in people with type 2 diabetesDiabetes Mellitus, Type 2MedDRA version: 21.1Level: LLTClassification code 10045242Term: Type II diabetes mellitusSystem Organ Class: 100000004861EUCTR2020-000299-39-SKovo Nordisk A/S1,620
