A 52-week study comparing the efficacy and safety of once weekly IcoSema and once weeklyinsulin icodec, both treatment arms with or without oral anti-diabetic drugs, in participants withtype 2 diabetes inadequately controlled with daily basal insulin. COMBINE 1 - COMBINE 1

ovo Nordisk AS0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年4月1日

试验速览

阶段: 3 期
状态: 进行中（未招募）
发起方

研究概览入排标准研究者记录与标识符相似试验

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

入选标准

•1) Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
•2) Male or female.
•3) Age above or equal to 18 years at the time of signing informed consent.
•4) Diagnosed with type 2 diabetes mellitus greater than or equal to 180 days before screening.
•5) HbA1c of 7.0-10.0% (53.0-85.8 mmol per mol) (both inclusive) as assessed by central laboratory on the day of screening.
•6) Treated with once daily or twice-daily basal insulin (neutral protamine hagedorn insulin, insulin degludec, insulin detemir, insulin glargine 100 units per mL, or insulin glargine 300 units per mL) 20-80 units per day greater than or equal to 90 days before screening. Short term bolus insulin treatment for a maximum of 14 days before screening is allowed, as is prior insulin treatment for gestational diabetes. The treatment can be with or without any of the following anti-diabetic drugs with stable dose greater than or equal to 90 days before screening: Metformin, Sulfonylureasa, Meglitinides (glinides)a, DPP-4 inhibitorsa, Sodium-glucose co-transporter 2 inhibitors, Alpha-glucosidase-inhibitors, Thiazolidinediones, Marketed oral combination products only including the products listed above.
•7) Body mass index (BMI)lesser than or equal to 40.0 kg per m2.
•8) Not currently using real time continuous or flash glucose monitoring.

排除标准

•1. Known or suspected hypersensitivity to randomised treatment or related products.
•2. Previous participation in this study. Participation is defined as signed informed consent.
•3. Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing
•potential and not using a highly effective contraceptive method, as defined in Appendix 4.
•4. Participation (i.e., signed informed consent) in any interventional, clinical study within 90 days
•before screening.
•Note: Simultaneous participation in a study with the primary objective of evaluating an
•approved or non-approved investigational medicinal product for prevention or treatment of
•COVID-19 disease or postinfectious conditions is allowed if the last dose of the investigational
•medicinal product has been received more than 30 days before screening in the current study
•and if simultaneous participation is allowed by local authorities.
•5. Any disorder, except for conditions associated with T2D, which in the investigator’s opinion
•might jeopardise participant’s safety or compliance with the protocol.
•6. 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).
•7. Treatment with any medication for the indication of diabetes or obesity other than stated in the
•inclusion criteria within 90 days before screening.
•8. Any episodesa of diabetic ketoacidosis within 90 days before screening.
•9. Personal or first-degree relative(s) history of multiple endocrine neoplasia type 2 or medullary
•thyroid carcinoma.
•10. Presence or history of pancreatitis (acute or chronic) within 180 days before screening.
•11. Any of the following: Myocardial infarction, stroke, hospitalization for unstable angina pectoris
•or transient ischaemic attack within 180 days before screening.
•12. Chronic heart failure classified as being in New York Heart Association Class IV at screening.
•13. Planned coronary, carotid or peripheral artery revascularisation.
•14. Renal impairment measured as estimated glomerular filtration rate value of
•< 30 ml/min/1.73 m2 at screening as defined by KDIGO 2012.20
•15. Impaired liver function, defined as alanine aminotransferase = 2.5 times or bilirubin > 1.5 times
•upper normal limit at screening.
•16. Known hypoglycaemic unawareness as indicated by the investigator according to Clarke’s
•questionnaire question 8.21.
•17. Recurrent severe hypoglycaemic episodes within the last year (12 months) as judged by the
•investigator.
•18. Inadequately treated blood pressure defined as systolic = 180 mmHg or diastolic = 110 mmHg
•at screening.
•19. 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, see 8.2.4.
•20. Presence or history of malignant neoplasm (other than basal or squamous cell skin cancer,
•in-situ carcinomas of the cervix, or in situ prostate cancer)

研究者

发起方

ovo Nordisk AS

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