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临床试验/JPRN-jRCT2031230600
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

研究者

发起方
takizaki Hiroshi

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