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
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