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Semaglutide: A Novel Oral Glucagon-Like Peptide Receptor Agonist for the Treatment of Type 2 Diabetes Mellitus.

Cardiol Rev · 2021

Last updated 2026-05-28

Semaglutide is the first oral GLP-1 drug approved by the FDA in 2019 for type 2 diabetes, offering an alternative to injectable options. It works by mimicking a natural hormone called GLP-1, which helps regulate blood sugar levels. Unlike earlier GLP-1 drugs like exenatide, which are injected, semaglutide comes in a pill form for patients who prefer not to use injections.

AI summary of the abstract below.

JournalCardiol Rev, 2021
Citations10
Relative citation ratio0.81
NIH percentile43
Molecules semaglutide
Conditions studied Type 2 Diabetes

Abstract

Diabetes mellitus (DM) is a complex and chronic condition that requires continuous medical care. Uncontrolled hyperglycemia can lead to serious microvascular and macrovascular complications, such as coronary artery disease, peripheral arterial disease, and stroke. Type 2 DM occurs when the pancreas is unable to produce adequate insulin to regulate glucose levels and when there is a decrease in sensitivity to insulin in the body. Insufficient glucagon-like peptide (GLP-1), a normal body hormone, plays an important role in the pathophysiology of DM. The introduction of the GLP-1 receptor agonists expanded therapeutic options in achieving glycemic control in adult patients. In 2005, the US Food and Drug Administration approved exenatide as the first injectable formulation, which led to the advancement of other injectable formulations within the class of GLP-1 receptor agonists. In 2019, semaglutide was approved as the first oral GLP-1 receptor agonist addressing the unmet needs in patients who benefit from therapy with this therapeutic class yet are unwilling to use an injectable drug. This article will provide an overview of the GLP-1 receptor agonists, including the pharmacology of semaglutide, its clinical evidence and role in therapy in type 2 DM.

Verbatim abstract via PubMed 32897887 ↗

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