跳至主要内容
临床试验/NCT07212868
NCT07212868招募中1 期

The Role of Glucagon in Glucose Metabolism in Humans With and Without Bariatric Surgery

The University of Texas Health Science Center at San Antonio4 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2026年2月25日最近更新:
干预措施

试验速览

阶段
1 期
状态
招募中
入组人数
150
试验地点
4
主要终点
Glycemc response to meal ingestion

研究概览

简要总结

The goal of this study is to understand the role of glucagon signal on glucose metabolism in individuals with and without bariatric surgery. The study is involved with measuring glucose metabolism with glucagon infusion and glucagon receptor blockade. We use an investigational drug called REMD 477. "Investigational" means that the has not yet been approved by the U.S. Food & Drug Administration (FDA). REMD-477 is a monoclonal antibody (an antibody made by cloning a unique white blood cell) that blocks the effect of glucagon.

详细描述

Participants will be screened, and if eligible will be enrolled for metabolic studies for two separate aims. In aim 1, they undergo glucose clamp study with and without glucagon infusion.

In aim 2, they undergo 2-day meal studies with and without a single dose administration of investigational drug, REMD 477 using a small needle subcutaneously. During these studies glycemic profile will be evaluated using CGM (Continuous glucose monitoring). Participants will also have a blood draw for liver enzymes8 weeks after the administration of REMD 477.

Participants will spend up to 3- 6 months participating in any pair study.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Other
盲法
Single (Participant)

盲法说明

Masking for participants

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

入选标准

  • Provision of signed and dated informed consent form from participant.
  • Male or female, ≤65 and ≥18 years old
  • Subjects with history of gastric bypass surgery and sleeve gastrectomy more than a year since surgery and non-surgical subjects without history of gastrointestinal (GI) surgery
  • Willing to adhere to the study intervention regimen
  • Female subjects of childbearing potential must have a negative pregnancy test at screening and all the study visits, and must not be lactating
  • Females of childbearing potential who are sexually active with a nonsterilized male partner must use at least one highly effective method of contraception from screening and must agree to continue using such precautions during the study.It is strongly recommended for the male partner of a female subject to also use male condom plus spermicide throughout this period. Cessation of contraception after this point should be discussed with a responsible physician. Periodic abstinence, the rhythm method, and the withdrawal method are not acceptable methods of contraception.

排除标准

  • Pregnancy/lactation
  • Current GI obstruction or chronic diarrhea
  • Subjects who are not within the age range of 18- 65 years.
  • Evidence of active cardiorespiratory, hepatic, gastrointestinal or renal disease.
  • History of allergy to the administered drugs.
  • History of, or any existing condition that, in the opinion of the investigator, would interfere with evaluation of the investigational product, put the subject at risk, influence the subject's ability to participate or affect the interpretation of the results of the study and/or any subject unable or unwilling to follow study procedures.
  • Substance dependence or history of alcohol abuse and/or excess alcohol intake
  • Patients on ketogenic diet
  • Prisoners or institutionalized individuals
  • AST (SGOT) > 3 times upper limit of normal
  • ALT (SGPT) > 3 times upper limit of normal
  • History of clinical hypoglycemia documents based on Whipples' triad (ONLY for Aim 2)

研究组 & 干预措施

Mixed Meal study with and without glucagon receptor antagonist

Experimental

Mixed meal test conducted with a sequential design of receiving a single dose subcutaneous injection of glucagon receptor antagonist or placebo.

干预措施: REMD-477 versus Placebo (Drug)

Pancreatic clamp (hypoglycemia and hyperglycemic) with and without glucagon infusion

Other

A cross-over study to compare the effect of glucagon infusion on glucose metabolism measured during clamp studies

干预措施: Exogenous glucagon versus saline infusion (Other)

结局指标

主要结局

Glycemc response to meal ingestion

时间窗: 0 to 240 minutes

Changes in glucose response to meal ingestion occurred by administration of glucagon receptor antagonist (GRA).

Endogenous glucose production (EGP) during clamp studies

时间窗: 0 to 240 minutes

Changes in EGP (measured by tracer technique) with and without glucagon infusion

次要结局

  • Prandial glucose kinetics(Baseline to 240 minutes)
  • Plasma GLP-1, GIP, insulin and glucagon concentrations(0 to 240 minutes)
  • Glucose clearance and insulin and glucagon concentrations during clamp studies(0 to 240 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marzieh Salehi

Professor

The University of Texas Health Science Center at San Antonio

研究点 (4)

Loading locations...

相似试验