Early-phase and translational research on retatrutide, a GLP-1/GIP/glucagon tri-agonist in development for obesity and metabolic disease.
Also called Retatrutide, LY3437943, triple incretin agonist
Sources: 12 new papers · 5 key papers · updated Oct 20, 2026
Unverified · drafted by AI from the sources cited below
Glucagon-like peptide-1 receptor agonists are compounds that stimulate the activity of GLUCAGON-LIKE PEPTIDE-1 RECEPTOR.1 They were initially developed to treat type 2 diabetes and are highly effective for glycaemic control.2
Pharmacy students’ knowledge and attitudes regarding GLP-1 receptor agonist adverse effects in obesity management: a cross-sectional study
Libyan Journal of Medicine — Khojah A — Oct 2026
GLP-1 receptor agonist initiation and risk of psychiatric hospitalisation and emergency department presentation in adults with schizophrenia and type 2 diabetes in the USA: an observational cohort study using electronic health records data
The Lancet Psychiatry — Davoodian N — Oct 2026
Incretin Mimetics and Alcohol‐Related Outcomes: A Structured Narrative Review
Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy — Goodyear C — Oct 2026
The effects of improved access to diabetes medications on risk of Alzheimer's disease and related dementias
Alzheimer s & Dementia — Barthold D — Oct 2026
Global Landscape and Thematic Evolution of Selective GLP ‐1 Receptor Agonists and GLP ‐1–Based Multi‐Receptor Agonists in Type 2 Diabetes Mellitus: A Bibliometric Analysis
Endocrinology Diabetes & Metabolism — Wang Y — Sep 2026
Gastrointestinal adverse effects of GLP‐1 receptor agonists and dual GIP/GLP‐1 receptor agonists: A narrative expert review of approved therapies, oral formulations, and pipeline agents
Nutrition in Clinical Practice — Vikash F — Sep 2026
Real-world treatment patterns and cost per patient achieving treatment targets among tirzepatide and semaglutide initiators in US patients with type 2 diabetes
Journal of Managed Care & Specialty Pharmacy — Hoog M — Sep 2026
Study on the Regulatory Mechanism of GLP-1 Receptor Agonist Liraglutide in Diabetic Corneal Epithelial Wound Healing
Investigative Ophthalmology & Visual Science — Liu X — Sep 2026
Return on investment of SGLT2 inhibitors and GLP-1 receptor agonists: Implications of real-world use for managed care
Journal of Managed Care & Specialty Pharmacy — Rapp H — Sep 2026
GLP‐1R agonist semaglutide protects human forebrain organoids from cholesterol‐induced neurotoxicity
Alzheimer s & Dementia — Yu F — Sep 2026
Semaglutide versus placebo in patients with heart failure and mildly reduced or preserved ejection fraction: a pooled analysis of the SELECT, FLOW, STEP-HFpEF, and STEP-HFpEF DM randomised trials
The Lancet — Kosiborod M
312 citations · 2024 · among the most cited on Retatrutide
GLP-1 receptor agonists and next-generation incretin-based medications: metabolic, cardiovascular, and renal benefits
The Lancet — Nauck M
118 citations · 2026 · among the most cited on Retatrutide
Risk of Heart Failure in Patients With Nonalcoholic Fatty Liver Disease
Journal of the American College of Cardiology — Mantovani A
115 citations · 2022 · among the most cited on Retatrutide
Therapeutic Manipulation of Myocardial Metabolism
Journal of the American College of Cardiology — Honka H
100 citations · 2021 · among the most cited on Retatrutide
Cardiovascular Effects and Tolerability of GLP-1 Receptor Agonists
Journal of the American College of Cardiology — Galli M
96 citations · 2025 · among the most cited on Retatrutide
A clinical question appears here only when its condition matches this topic, an outcome and a comparator were extracted from the studies, at least two studies and a patient count are on file, and the certainty is low or higher.
Supports benefit, no benefit shown, and mixed describe the direction of the measured effect. No benefit shown means the evidence does not support a benefit. It is not a finding of harm. Too little evidence means the question did not clear that bar.
Study count, RCT count, and patient count are separate. The patient total adds only studies that are linked into a study family and whose sample size is not flagged as implausible. A reversal is listed only when at least one randomized trial sits on each side of the change.
The overview is drafted from the guideline recommendations, trials, papers, and questions on this page, and every sentence has to cite one of them. It stays unverified until an NPI-verified clinician or a Synapse admin approves it. Approving records that person's name.