JPRN-jRCT2031230600尚未招募3 期
A 40-week study comparing the efficacy and safety of once weekly IcoSema and daily insulin glargine 100 units/mL in participants with type 2 diabetes inadequately controlled on oral anti-diabetic drugs. (NN1535-4988:COMBINE 4) - COMBINE 4
takizaki Hiroshi0 个研究点目标入组 60 人开始时间: 2024年1月26日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
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
- •1. Male or female and age above or equal to 18 years at the time of signing the informed consent.
- •2. Diagnosed with T2D >=180 days before screening.
- •3. HbA1c >=8.0% (>=64.0 mmol/mol) as assessed by central laboratory on the day of screening.
- •4. Insulin naive. Short term insulin treatment for a maximum of 14 consecutive days before screening is allowed, as is prior insulin treatment for gestational diabetes.
- •5. Currently treated with 1-3 OADs with stable daily doses >= 90 days before screening comprising any of the following anti-diabetic drug(s) at effective or maximum tolerated dosea
- •-Metformin
- •-Sulfonylureasb
- •-Meglitinides (glinides)
- •-DPP-4 inhibitorsb
- •-Sodium-glucose co-transporter 2 inhibitors
- •-Alpha-glucosidase-inhibitors
- •-Thiazolidinediones
- •-Marketed oral combination products only including the products listed above.6. Body mass index (BMI) <=40.0 kg/m2.
排除标准
- •1. Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using highly effective contraceptive method.
- •2. Anticipated initiation or change in concomitant medication (for more than 14 consecutive days) known to affect weight or glucose metabolism (e.g. treatment with orlistat, thyroid hormones, or systemic corticosteroids).
- •3. Any episodesa of diabetic ketoacidosis or treatment with any medication for the indication of diabetes or obesity other than stated in the inclusion criteria within 90 days before screening.
- •4. Presence or history of pancreatitis (acute or chronic) within 180 days before screening.
- •5. Any of the following: Myocardial infarction, stroke, hospitalization for unstable angina pectoris or transient ischaemic attack within 180 days before screening.
- •6. Chronic heart failure classified as being in New York Heart Association Class IV at screening.
- •7. Recurrent severe hypoglycaemic episodes within the last year (12 months) as judged by the investigator.
- •8. Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by a fundus
- •examination performed within the past 90 days before screening or in the period between screening and randomisation. Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination
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