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Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM

2026年5月1日 更新者:Wang Weiqing、Shanghai Jiao Tong University School of Medicine

A Single -Center, Randomized, Double-blind, Placebo-controlled Proof of Exploratory Study Evaluating the Efficacy, Safety, and Tolerability of CS0159 Combined With Semaglutide in MAFLD Patients With Obesity and T2DM

This is an exploratory study evaluating CS0159 in combination with Semaglutide in metabolic dysfunction-associated fatty liver disease (MAFLD) patients with obesity and type 2 diabetes (T2DM).

研究概览

详细说明

This is an exploratory study to evaluate the efficacy, safety, and tolerability of CS0159 in combination with Semaglutide in MAFLD patients with obesity and T2DM. Approximately 30 patients were randomly assigned to two groups in a 1:1 ratio for treatment for 12 weeks.

研究类型

介入性

注册 (估计的)

30

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • 1. Age≥18 and ≤65 years, male or female.
  • 2. MRI-PDFF ≥10% within 3 months prior to randomized.
  • 3. Diagnosis of T2DM.
  • 4. HbA1c: 7.0%-10.5%.
  • 5. FPG: 7.0-13.3 mmol/L.
  • 6. BMI: 30-45 kg/m2.
  • 7. Subjects control blood glucose only by lifestyle intervention for at least 3 months before the screening period.
  • 8. Willing to maintain consistent diet and exercise habits throughout the entire study, and adhere to the study protocol for timely administration of the study drug, and timely self-monitoring of blood glucose and recording.
  • 9. Can understand the research content, follow the research protocol, and voluntarily sign the ICF.

Exclusion Criteria:

  • 1. ALT≥2.5×ULN, AST≥2.5×ULN, TBil≥2×ULN, creatinine (Cr) ≥1.5×ULN and Serum creatinine clearance<60 mL/min, PLT<100×10^9/L, INR >1.3, ALB <3.5 g/dL.
  • 2. Use of glucose-lowering medication in the 3 months prior to randomization.
  • 3. Weight loss ≥ 5% in the 3 months prior to randomization or ≥10% in the 6 months prior to randomization or use of other weight-lowering drugs, corticosteroids, and etc.
  • 4. History of allergy to glucagon-like peptide-1 receptor agonists (GLP-1RA) medications, currently in an allergic state, having allergic conditions, or history of allergies to ≥2 substances.
  • 5. Subjects with T1DM, monogenic diabetes, diabetes caused by pancreatic damage, or other secondary diabetes.
  • 6. Subjects with a history of severe pruritus.
  • 7. Uncontrolled and potentially unstable diabetic retinopathy or maculopathy.
  • 8. Thyroid C-cell tumour or family history, multiple endocrine neoplasia type 2 or family history.
  • 9. History of acute or chronic pancreatitis.
  • 10. Subjects with Child-Pugh class B or C grade cirrhosis.
  • 11. HBsAg positive, HCV Ab positive, HIV Ab positive, TP Ab positive.
  • 12. Arrhythmias, male QTc≥450 ms, or female QTc≥470 ms. Or cardiovascular disease for which the researcher has assessed that participation in the trial is not appropriate.
  • 13. Diseases that interfere with the absorption, distribution, metabolism or excretion.
  • 14. Gastrointestinal diseases that affect food digestion and absorption.
  • 15. Use moderate or strong inhibitors or inducers of cytochrome P450 enzyme (CYP3A4 enzyme) within the first 14 days of randomization and throughout the entire trial period.
  • 16. History of malignant tumors within the first 5 years of randomization.
  • 17. Serious hypoglycemic events occurring ≥ 3 times within 12 weeks prior to administration, or acute and severe metabolic disorder occurred within 12 weeks prior to administration.
  • 18. Drug abuse or alcohol abuse within the first 6 months of randomization.
  • 19. Poor blood pressure control.
  • 20. Mental illness, epilepsy.
  • 21. Patients with uncontrollable severe infectious diseases before randomization.
  • 22. Pregnant, planned pregnancy or breastfeeding.
  • 23. Participated in other clinical trials in the first three months of randomization.
  • 24. Any condition that in the judgement of the researcher precludes participation.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
有源比较器:4mg CS0159
4mg CS0159 (oral, once daily) + 0.5mg Semaglutide (subcutaneous injection, once weekly) for 12 weeks
The intervention will include a 12-week treatment period. During the 12-week treatment period, subjects will receive 4mg CS0159 (oral, once daily).
The intervention will include a 12-week treatment period. During the 12-week treatment period, subjects will receive 0.5mg Semaglutide (subcutaneous injection, once weekly).
安慰剂比较:CS0159 Placebo
CS0159 placebo (oral, once daily) + 0.5mg Semaglutide (subcutaneous injection, once weekly) for 12 weeks
The intervention will include a 12-week treatment period. During the 12-week treatment period, subjects will receive 0.5mg Semaglutide (subcutaneous injection, once weekly).
The intervention will include a 12-week treatment period. During the 12-week treatment period, subjects will receive CS0159 placebo (oral, once daily).

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Percentage change in body weight relative to baseline
大体时间:Baseline to 12 weeks
Evaluate the percentage change in body weight relative to baseline after 12 weeks of treatment.
Baseline to 12 weeks
Changes in energy expenditure
大体时间:Baseline to 12 weeks
The impact of the patient's energy expenditure change relative to the baseline after 12 weeks, assessed by whole-room indirect calorimetry (metabolic chamber).
Baseline to 12 weeks

次要结果测量

结果测量
措施说明
大体时间
Change in patient's weight relative to the baseline
大体时间:Baseline to 12 weeks
Evaluation of the change in patient's weight relative to the baseline after 12 weeks with CS0159
Baseline to 12 weeks
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
大体时间:Baseline to 12 weeks
Evaluate the safety and tolerability of CS0159 combined with semaglutide during a 12-week treatment period
Baseline to 12 weeks
Change in patient's glucose oxidation
大体时间:Baseline to 12 weeks
Evaluation of the effect of CS0159 on glucose and lipid oxidation in patients relative to baseline after 12 weeks of administration, assessed by whole-room indirect calorimetry (metabolic chamber).
Baseline to 12 weeks
Change in patient's lipid oxidation
大体时间:Baseline to 12 weeks
Evaluation of the effect of CS0159 on glucose and lipid oxidation in patients relative to baseline after 12 weeks of administration, assessed by whole-room indirect calorimetry (metabolic chamber).
Baseline to 12 weeks
Percentage change in HbA1c relative to baseline
大体时间:Baseline to 12 weeks
Evaluate the percentage change in glycated hemoglobin (HbA1c) relative to baseline after 12 weeks of treatment.
Baseline to 12 weeks
Changes relative to baseline in BMI
大体时间:Baseline to 12 weeks
Changes in body mass index (BMI) relative to baseline after 12 weeks of administration
Baseline to 12 weeks
Changes relative to baseline in body composition
大体时间:Baseline to 12 weeks
Changes in body composition analysis relative to baseline after 12 weeks of administration
Baseline to 12 weeks
Changes relative to baseline in waist circumference
大体时间:Baseline to 12 weeks
Changes in waist circumference relative to baseline after 12 weeks of administration
Baseline to 12 weeks
Changes relative to baseline in waist to hip ratio (WHR)
大体时间:Baseline to 12 weeks
Changes in waist to hip ratio (WHR) relative to baseline after 12 weeks of administration
Baseline to 12 weeks
Changes relative to baseline in serum liver function parameters
大体时间:Baseline to 12 weeks
including alanine aminotransferase, aspartate aminotransferase, glutamyltransferase, alkaline phosphatase, lactate dehydrogenase, total bilirubin, direct bilirubin, total protein, albumin, and total bile acid.
Baseline to 12 weeks
Changes relative to baseline in serum lipid profile
大体时间:Baseline to 12 weeks
including serum triglycerides, total cholesterol, low-density lipoprotein cholesterol and high-density lipoprotein cholesterol.
Baseline to 12 weeks
Changes relative to baseline in plasma glucose levels
大体时间:Baseline to 12 weeks
including fasting plasma glucose and 2-hour post-prandial plasma glucose
Baseline to 12 weeks
Changes relative to baseline in serum insulin levels
大体时间:Baseline to 12 weeks
including fasting serum insulin and 2-hour post-prandial serum insulin
Baseline to 12 weeks
Changes in peripheral blood metabolomics and proteomics relative to baseline
大体时间:Baseline to 12 weeks
Changes in peripheral blood metabolomics and proteomics relative to baseline after 12 weeks of administration
Baseline to 12 weeks
Changes in fecal metabolites, gut microbiota homeostasis, and fecal gut microbiota metagenome relative to baseline
大体时间:Baseline to 12 weeks
Changes in fecal metabolites, gut microbiota homeostasis, and fecal gut microbiota metagenome relative to baseline after 12 weeks of administration
Baseline to 12 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月1日

初级完成 (估计的)

2026年11月30日

研究完成 (估计的)

2026年12月31日

研究注册日期

首次提交

2026年3月15日

首先提交符合 QC 标准的

2026年5月1日

首次发布 (实际的)

2026年5月6日

研究记录更新

最后更新发布 (实际的)

2026年5月6日

上次提交的符合 QC 标准的更新

2026年5月1日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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