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临床试验/JPRN-jRCT2031220734
JPRN-jRCT2031220734进行中(未招募)3 期

Efficacy and safety of cagrilintide s.c. 2.4 mg in combination with semaglutide s.c. 2.4 mg (CagriSema s.c. 2.4 mg/2.4 mg) once-weekly in East Asian participants with overweight or obesity(NN9838-4762) - REDEFINE 5

Sudo Yuki0 个研究点目标入组 320 人开始时间: 2023年3月26日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
320

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

  • Male or female
  • -Age >=18 years at the time of signing informed consent
  • a) BMI >=27.0 kg/m2 with >=2 obesity-related complications or
  • b) BMI >=35.0 kg/m2 with >=1 obesity-related complication. At least one complication should be hypertension, dyslipidaemia or T2D.
  • Diabetes-related for participant with T2D
  • -Diagnosed with T2D >= 180 days before screening
  • -HbA1c 7.0-10.0%(53-86 mmol/mol))(both inclusive) as measured by central laboratory at screening
  • -Treatment with either lifestyle intervention, or treatment with 1-3 marketed oral antidiabetic drugs (OAD)s (metformin, alfa-glucosidase inhibitors [AGI], glinides, sodium-glucose co-transporter 2 inhibitor [SGLT2i]), thiazolidinediones, or sulphonylureas [SU] as a single agent or in combination) according to local label
  • -Treatment with oral antidiabetic drugs should be stable (same drug(s), dose and dosing frequency) for at least 90 days before screening.

排除标准

  • Obesity-related
  • -Treatment with any medication prescribed for the indication of obesity or weight management within 90 days before screening
  • Glycaemia-related for participant without T2D
  • -HbA1c >=6.5% (48 mmol/mol) as measured by the central laboratory at screening
  • -History of type 1 or type 2 diabetes
  • Diabetes-related for participant with T2D
  • -Renal impairment with estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m2 as measured by central laboratory at screening
  • -Clinically significant or severe hypoglycaemia within 6 months of screening or history of hypoglycaemia unawareness
  • -Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by a fundus examination performed within 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
Sudo Yuki

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