GLP-1-based therapies for diabetes, obesity and beyond.
Nat Rev Drug Discov · 2025
Last updated 2026-05-28GLP-1-based drugs like semaglutide and tirzepatide help people with type 2 diabetes and obesity by improving blood sugar control and promoting weight loss, while also reducing risks related to heart and kidney health. New versions of these drugs aim to offer better weight loss results, fewer side effects, and more convenient dosing options. Researchers are also exploring whether these drugs could treat other conditions like liver disease, arthritis, and high blood pressure, though these uses are still being studied.
AI summary of the abstract below.
| Journal | Nat Rev Drug Discov, 2025 |
|---|---|
| Citations | 109 |
| Relative citation ratio | 43.24 |
| Molecules | — |
| Conditions studied | Type 2 Diabetes, Obesity |
Abstract
Glucagon-like peptide 1 (GLP-1)-based therapies, such as semaglutide and tirzepatide, represent highly effective treatment options for people with type 2 diabetes and obesity, enabling effective control of glucose and weight loss, while reducing cardiovascular and renal morbidity and mortality. The success of these medicines has spurred development of next-generation GLP-1-based drugs, promising greater weight loss, improved tolerability and additional options for the route and frequency of dosing. This Review profiles established and emerging GLP-1-based medicines, discussing optimization of pharmacokinetics and tolerability, engagement of new therapeutically useful pathways and safety aspects. Structurally unique GLP-1-based medicines that achieve substantially greater and rapid weight loss may impact musculoskeletal health, providing a rationale for therapeutics that more selectively target adipose tissue loss while preserving muscle mass and strength. Ongoing clinical trials in peripheral vascular disease, neuropsychiatric and substance use disorders, metabolic liver disease, arthritis, hypertension and neurodegenerative disorders may broaden indications for GLP-1-based therapeutics.
Verbatim abstract via PubMed 40281304 ↗