Genetics of the Acute Response to Oral Semaglutide (GAROS)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 1,000
- 试验地点
- 1
- 主要终点
- Glycemic measures - change in HbA1c (%)
研究概览
简要总结
The study aims to investigate the genetic basis of the response to short-term (3 months) orally administered semaglutide treatment, in terms of improving metabolic parameters, including the hormonal response to a standardized meal, and changes in body composition and liver steatosis. In the study, parameters such as fasting and 2-hour glucose during OGTT, HbA1c, body fat mass, body weight, total cholesterol, HDL and LDL, triglycerides, HOMA-IR, Matsuda Index and liver steatosis will be assessed. All the patients will undergo genome-wide genotyping. Moreover, in a subset of participants, muscle and fat biopsies will be performed, before and after the treatment, and liver, muscle and pancreas fat content will be assessed using MRI.
详细描述
Each subject will participate in the following visits:
Visit v1 (screening) - for each patient, fasting venous blood will be collected and an oral glucose tolerance test (OGTT) will be performed - with blood samples taken 30, 60, 90 and 120 minutes after drinking the glucose solution. Fasting blood samples will be used to measure basic metabolic parameters (including glucose, lipid profile, HbA1c, AST, ALT, GGTP, electrolytes, blood count, the presence of antibodies against beta-cell antigens, TSH), and from blood collected at each time point during the OGTT glucose and insulin concentrations will be measured. Each patient will also undergo a detailed body composition analysis using bioimpedance and DXA. In addition, during the visit, each participant will receive a continuous glucose monitoring system (CGM) and an accelerometer to measure physical activity for a period of 10-14 days.
Visit v2 (14-30 days after v1)- during the visit, each patient will undergo a mixed meal tolerance test (MMTT), with blood samples taken 5, 10, 15, 30, 60, 90, 120, 180 minutes after eating the meal, along with a non-invasive measurement of resting energy expenditure (RMR). After the end of the test, the patient will receive semaglutide in two marked doses: 3 mg and 7 mg, along with instructions on how to take them and a diary in which the drug intake and occurrence of side effects will be recorded.
Visit v3 - four weeks after starting the semaglutide treatment. During the visit, fasting venous blood will be collected to measure basic metabolic parameters. Each patient will undergo a detailed body composition analysis using bioimpedance and DXA. During the visit, patients will receive semaglutide in the dose of 14 mg, along with instructions on how to take them and a diary in which the drug intake and occurrence of side effects will be recorded.
Visit v4 - twelve weeks after starting semaglutide treatment. Similar to visit 1 (OGTT).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Informed consent was given before any study-related action on the subject.
- •Age: 18-65 years old
- •Body mass index (BMI) >30 kg/m2 or >27 kg/m2 when accompanied by prediabetes, diagnosed according to the criteria of the American Diabetes Association
排除标准
- •Patients diagnosed with a serious chronic disease, including:
- •Ischemic heart disease
- •Heart failure (NYHA class III-IV)
- •Severe renal insufficiency (eGFR <30 ml/min)
- •Severe liver diseases
- •Inflammatory bowel disease
- •Diabetic gastroparesis
- •Cancer - currently or in the last five years prior to screening
- •Chronic obstructive pulmonary disease
- •History of mental illness, major depression or other severe mental disorders
- •Use of any medications with clinically-proven significant weight gain or loss effects
- •History of undergoing bariatric surgery or other surgery involving the stomach that could affect the absorption of the study drug (according to the investigator's opinion)
- •History of idiopathic acute pancreatitis
- •A family or personal history of multiple endocrine neoplasia type 2 (MEN2) or medullary thyroid cancer
- •For women - pregnancy, breastfeeding or planning pregnancy.
- •Women of childbearing age who are not using highly effective methods of contraception
- •Known or suspected hypersensitivity to the test product
研究组 & 干预措施
Semaglutide (oral)
In this study, each participant will receive a regimen of oral semaglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist, for a duration of twelve weeks. The dosage will begin at 3 mg/day for weeks 1-2, gradually increasing to 7 mg/day for weeks 3-4, 14 mg/day for weeks 5-6, 28 mg/day for weeks 7-8, and finally, to 42 mg/day for the last four weeks (weeks 9-12).
干预措施: Semaglutide Pill (Drug)
结局指标
主要结局
Glycemic measures - change in HbA1c (%)
时间窗: 1 and 3 months
Investigators will measure the change in HbA1c concentration between Visit 2, Visit 3 and Visit 4 as an index of Semaglutide response, and compare them by genotype at selected loci.
Body composition - change in body weight (kg)
时间窗: 1 and 3 months
Investigators will measure the change in body weight measures between Visit 2, Visit 3 and Visit 4 as an index of Semaglutide response, and compare them by genotype at selected loci.
次要结局
- Glycemic measures - change in 2-hour glucose (in mg/dl)(1 and 3 months)
- Glycemic measures - change in fasting glucose (in mg/dl)(1 and 3 months)
- Body composition - change in body fat content (kg)(1 and 3 months)
- Body composition - change in lean body mass content (kg)(1 and 3 months)