GLPwatch

An overview of new GLP-1 receptor agonists for type 2 diabetes.

Expert Opin Investig Drugs · 2016

Last updated 2026-05-28

New GLP-1 drugs for type 2 diabetes are being developed to require less frequent injections or be taken as pills instead of shots. These drugs help control blood sugar and reduce weight, but their effects on heart health are still being studied, with some related medications showing no clear benefit for heart risks.

AI summary of the abstract below.

JournalExpert Opin Investig Drugs, 2016
Citations39
Relative citation ratio1.61
NIH percentile67
Molecules
Conditions studied Type 2 Diabetes

Abstract

INTRODUCTION: The increasing prevalence of type 2 diabetes mellitus (T2DM) and the eventual need for multiple medications in most patients stimulated the development of new drug classes to reduce plasma glucose levels. The GLP-1 receptor agonists (GLP-1RAs) are established as an option for treatment of T2DM after metformin. They are also effective in reducing body weight but current GLP-1RAs have to be given by subcutaneous injection daily or once weekly. AREAS COVERED: This review focuses on the new GLP-1RAs currently undergoing development, some of which require less frequent subcutaneous administration and others that are being developed in oral formulations that may favor patient adherence. EXPERT OPINION: The new GLP-1RAs may have the benefit of requiring less frequent subcutaneous dosing or being active by oral administration. However, cardiovascular outcome trials have shown that DPP4 inhibitors are neutral for cardiovascular events and the first cardiovascular outcome trial with lixisenatide reported similar results, whereas the trial with the SGLT2 inhibitor empagliflozin showed a reduction in cardiovascular events. These findings in patients with high cardiovascular risk may favor the use of SGLT2 inhibitors as a second line treatment after metformin but there should still be an important role for novel GLP-1RAs, especially when weight reduction is required.

Verbatim abstract via PubMed 26587691 ↗