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The GLP-1 Hub

GLP-1 receptor agonists are the most-studied, most-prescribed, and most consequential class of peptides in modern medicine. This hub covers the approved drugs, the emerging incretin and glucagon co-agonists in trials, head-to-head comparisons, practical guides, and the research updates that are reshaping the field in 2026.

What is a GLP-1?

Glucagon-like peptide-1 (GLP-1) is a gut hormone released by intestinal L-cells in response to nutrient ingestion. It signals the pancreas to release insulin in proportion to glucose, slows gastric emptying, and engages central appetite circuits. GLP-1 receptor agonists are drugs that mimic this hormone — typically modified peptides with extended half-life, more recently joined by small-molecule oral agonists and antibody-conjugate hybrids.

The class has expanded considerably since semaglutide's 2017 approval. Today the discussion includes single GLP-1 agonists (semaglutide, liraglutide, dulaglutide), dual GIP/GLP-1 agonists (tirzepatide), GLP-1/glucagon dual agonists (survodutide, mazdutide, pemvidutide), triple GIP/GLP-1/glucagon agonists (retatrutide), oral non-peptide GLP-1s (orforglipron), and antibody-peptide conjugates with GIP-receptor antagonism (MariTide). Each represents a different bet on what biology drives the strongest outcomes.

Approved drugs

In clinical trials

The next-generation incretin and glucagon co-agonist programs — including triple agonists, GIP-antagonist hybrids, oral non-peptide candidates, and MASH-focused dual agonists.

Comparison articles

Class breakdowns and head-to-head reads

Practical guides

For patients, clinicians, and engaged readers

Research updates

Cardiovascular, renal, and latest trial readouts

How to use this hub

Start with the semaglutide and tirzepatide peptide pages for the foundation. Move to single vs dual vs triple agonists for the class framework. The practical guides on muscle preservation, side effects, and long-term use are aimed at people actively using or considering GLP-1 therapy. The pipeline and research articles are for readers tracking how the field evolves.