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In January 2025, the Food and Drug Administration (FDA) approved a brand of semaglutide to reduce the risk of both cardiovascular death and worsening kidney disease in people with Type 2 diabetes and chronic kidney disease

For example, a phase III trial of semaglutide aims to evaluate its effects on MASH resolution, fibrosis improvement, and survival outcomes over an extended period

11 Whole brain cFos expression in response to semaglutide, MK-801, GLP-1 and GLP-1MK-801

A review upon medicinal perspective and designing rationale of DPP-4 inhibitors

Results of the LEADER and SUSTAIN-6 trials: cardiovascular outcomes with GLP-1 receptor agonists