A 26-week trial comparing the effect and safety of once weekly insulin icodec and once daily insulin glargine 100 units/mL, both in combination with bolus insulin with or without non-insulin anti-diabetic drugs, in subjects with type 2 diabetes on a basal-bolus regimen.(NN1436-4480) - ONWARDS4

ishida Hiroko0 个研究点目标入组 80 人开始时间: 2021年5月10日最近更新: 2024年4月1日

适应症

试验速览

暂无简介。

•1. Male or female aged above or equal to 18 years at the time of signing informed consent.
•2. Diagnosed with T2D>= 180 days prior to the day of screening.
•3. HbA1c from 7.0-10.0% (53.0 85.8 mmol/mol) both inclusive at screening confirmed by central laboratory analysis.
•4. 4.Treated with once daily basal insulin (neutral protamine hagedorn insulin, insulin degludec, insulin detemir, insulin glargine 100 units/mL, or insulin glargine 300 units/mL) and 2-4 daily injections of bolus insulin analog (insulin aspart, faster acting insulin aspart, insulin lispro, insulin glulisine) >= 90 days prior to the day of screening with or without any of the following anti-diabetic drugs/regimens with stable doses>= 90 days prior to screening:
•-Metformin
•-Sulfonylureas
•-Meglitinides (glinides)
•-DPP-4 inhibitors
•-SGLT2 inhibitors
•-Thiazolidinediones
•-Alpha-glucosidase inhibitors
•-Oral combination products (for the allowed individual oral anti-diabetic drugs)
•-Oral or injectable GLP-1-receptor agonists
•5. Body mass index (BMI) <= 40.0 kg/m2.

•1. Any episodesa of diabetic ketoacidosis within 90 days prior to the day of screening.
•2. Myocardial infarction, stroke, hospitalisation for unstable angina pectoris or transient ischaemic attack within 180 days prior to the day of screening.
•3. Chronic heart failure classified as being in New York Heart Association Class IV at screening.
•4. Anticipated initiation or change in concomitant medications (for more than 14 consecutive days) known to affect weight or glucose metabolism (e.g. treatment with orlistat, thyroid hormones, or corticosteroids).
•5. Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by a fundus examination performed within the past 90 days prior to 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.

发起方

ishida Hiroko