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临床试验/NCT07137585
NCT07137585进行中(未招募)1 期

Effects of RO7204239 on Insulin Sensitivity, Muscle Composition and Function in Participants Living With Type 2 Diabetes Mellitus and Overweight or Obesity: A Double-blind, Randomized, Placebo-controlled Study

Hoffmann-La Roche1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年9月30日最近更新:
干预措施

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
30
试验地点
1
主要终点
Change From Baseline in M-value in a Hyperinsulinemic Euglycemic Glucose Clamp (HEC) at Week 24

研究概览

简要总结

The main purpose of this study is to assess the effect of RO7204239 on insulin sensitivity versus placebo in participants with T2DM and obesity or overweight.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Participants with T2DM for at least 6 months, treated with diet, exercise and/or metformin alone or in combination with either dipeptidyl peptidase 4 (DPP-4) inhibitor or sodium-glucose co-transporter 2 (SGLT2) at stable dose for the last 3 months prior to study entry and with a HbA1c between ≤ 6.5% and ≤ 10%
  • Body mass index (BMI) within the range of 27.0 to 45.0 kilogram per meter square (kg/m2)
  • Stable body weight for the 3 months prior to screening
  • Participants on lipid-lowering or antihypertensive drugs must be on stable doses for at least 3 months

排除标准

  • Type 1 diabetes mellitus (DM), known latent autoimmune diabetes in adults, or people with an episode of ketoacidosis or hyperosmolar state requiring hospitalisation in 6 months prior to screening
  • Active proliferative diabetic retinopathy, diabetic maculopathy, or severe non-proliferative diabetic retinopathy requiring acute treatment
  • Uncontrolled comorbid conditions commonly associated with diabetes (for example, hypertension, hyperlipidaemia)
  • Severe hypoglycaemia within 6 months prior to screening visit
  • Current autonomic neuropathy as evidenced by neuropathic urinary retention, resting tachycardia, orthostatic hypotension, or diabetic diarrhea
  • Have evidence of a significant, uncontrolled endocrine abnormality (e.g., thyrotoxicosis and adrenal crises)
  • Are currently taking a central nervous system stimulant (e.g., Ritalin-SR), with the exception of caffeinated beverage
  • Have a known allergy, hypersensitivity, or intolerance to any component of the study treatment (i.e., RO7204239 / placebo) formulation
  • Blood donation of more than 500 milliliters (mL) within the past 3 months or blood transfusion or severe blood loss within 3 months prior to screening

研究组 & 干预措施

RO7204239

Experimental

Participants will receive RO7204239, Q4W, as a SC injection for 24 weeks.

干预措施: RO7204239 (Drug)

Placebo

Experimental

Participants will receive RO7204239 matching placebo, every 4 weeks (Q4W), as a subcutaneous (SC) injection for 24 weeks.

干预措施: Placebo (Drug)

结局指标

主要结局

Change From Baseline in M-value in a Hyperinsulinemic Euglycemic Glucose Clamp (HEC) at Week 24

时间窗: Baseline, Week 24

次要结局

  • Change From Baseline in Glycated Hemoglobin (HbA1c) at Week 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Glucose Metabolism Assessed Using Fasting Glucose Test at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Glucose Metabolism Assessed Using Insulin Test at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Glucose Metabolism Assessed Using C-peptide Test at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Blood Lipid Profiles at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Body Weight at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Waist Circumference at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Waist to Height Ratio at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Total Lean Tissue Volume and Total Adipose Tissue Volume From Abdominal Magnetic Resonance Imaging (MRI) at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Muscle Volume From Thigh Muscle MRI at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Change From Baseline in Muscle Fat Infiltration From Thigh Muscle MRI at Weeks 12 and 24(Baseline, Week 12, Week 24)
  • Number of Participants With Adverse Events (AEs)(Up to Week 48)
  • Number of Participants With Local and Systemic Injection Reactions(Up to Week 48)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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