Orforglipron as a Small-Molecule GLP-1 Receptor Agonist: A New Era of Incretin-Based Oral Therapy?
DOI:
https://doi.org/10.12775/QS.2026.56.72512Keywords
orforglipron, nonpeptide GLP-1 receptor agonists, body weight loss, obesity treatmentAbstract
Introduction: Facing the increasing number of people suffering from obesity, overweight and weight-related comorbidities, the development of medications that support weight loss is crucial. The currently available therapies based on glucagon-like peptide receptor 1 agonists (GLP-1 RAs) and glucose-dependent insulinotropic polypeptide/GLP-1 RAs allow for weight loss of 8-21% [1]. However, a significant factor reducing treatment adherence is subcutaneous route of administation by injection, as well ass - in the case of oral semaglutide – restrictive dosing requirements: the drug need to be taken at least 30 minutes before the first meal, beverage, or other oral medication in the morning and with no more than 120 ml of plain water [2].
Aim of the study: The purpose of this study is to review the safety and tolerance of orforglipron and to compare it with oral semaglutide based on ACHIEVE-3 clinical trail.
Material and Methods: Review and analysis of randomised clinical trials available on PubMed. We excluded phase 1 trials in analysis of patients with obesity without diabetes mellitus and patients with DM2. Notably, main clinical trials focusing on orforglipron were funded or supported by Eli Lilly and Company.
Conclusions: Orforglipron is definitely promising as a small-molecule GLP-1 receptor agonist. The therapy is effective in body weight reduction and results in a significant, dose-dependent reduction in HbA1c levels. With significant effect on weight loss, cardiometabolic parameters and improvement in glycemic profile, it can be used in combination with a reduced-calorie diet and increased physical activity in adults, as a weight-loss therapy or in patient with type 2 diabetes. However, all of the studies published so far on the innovative molecule of orforglipron were based on limited number of patients, therefore long-term safety, tolerance in a larger population and general long-term impact of orforglipron on health needs extensive studies.
References
1. Elmaleh-Sachs A, Schwartz JL, Bramante CT, Nicklas JM, Gudzune KA, Jay M. Obesity Management in Adults: A Review. JAMA. 2023;330(20):2000-2015. doi:10.1001/jama.2023.19897
2. Novo Nordisk Rybelsus (semaglutide) tablets [prescribing information]. Plainsboro, NJ, Novo Nordisk, 2019
3. World Health Organization. Obesity and Overweight. World Health Organization. Published May 7, 2025. https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight
4. Solsona-Vilarrasa E, Vousden KH. Obesity, white adipose tissue and cancer. FEBS J. 2025;292(9):2189-2207. doi:10.1111/febs.17312
5. Cefalu WT, Bray GA, Home PD, et al. Advances in the Science, Treatment, and Prevention of the Disease of Obesity: Reflections From a Diabetes Care Editors' Expert Forum. Diabetes Care. 2015;38(8):1567-1582. doi:10.2337/dc15-1081
6. Pratt E, Ma X, Liu R, et al. Orforglipron (LY3502970), a novel, oral non‐peptide glucagon‐like peptide‐1 receptor agonist: A Phase 1b, multicentre, blinded, placebo‐controlled, randomized, multiple‐ascending‐dose study in people with type 2 diabetes. Published online June 1, 2023. doi:https://doi.org/10.1111/dom.15150
7. Pratt E, Ma X, Liu R, et al. Orforglipron (LY3502970), a novel, oral non‐peptide glucagon‐like peptide‐1 receptor agonist: A Phase 1a, blinded, placebo‐controlled, randomized, single‐ and multiple‐ascending‐dose study in healthy participants. Published online June 21, 2023. doi:https://doi.org/10.1111/dom.15184
8. Overgaard RV, Navarria A, Ingwersen SH, Bækdal TA, Kildemoes RJ. Clinical Pharmacokinetics of Oral Semaglutide: Analyses of Data from Clinical Pharmacology Trials. Clinical Pharmacokinetics. 2021;60(10):1335-1348. doi:https://doi.org/10.1007/s40262-021-01025-x
9. Horn DB, Ryan DH, Kis SG, et al. Orforglipron, an oral small-molecule GLP-1 receptor agonist, for the treatment of obesity in people with type 2 diabetes (ATTAIN-2): a phase 3, double-blind, randomised, multicentre, placebo-controlled trial. The Lancet. Published online November 2025. doi:https://doi.org/10.1016/s0140-6736(25)02165-8
10. FDA Approves First New Molecular Entity Under National Priority Voucher Program. U.S. Food and Drug Administration. Published 2026. https://www.fda.gov/news-events/press-announcements/fda-approves-first-new-molecular-entity-under-national-priority-voucher-program
11. Commissioner's National Priority Voucher (CNPV) Pilot Program. U.S. Food and Drug Administration. Published 2026. https://www.fda.gov/industry/commissioners-national-priority-voucher-cnpv-pilot-program
12. Wharton S, Blevins T, Connery L, et al. Daily Oral GLP-1 Receptor Agonist Orforglipron for Adults with Obesity. N Engl J Med. 2023;389(10):877-888. doi:10.1056/NEJMoa2302392
13. Wharton S, Aronne LJ, Stefanski A, et al. Orforglipron, an Oral Small-Molecule GLP-1 Receptor Agonist for Obesity Treatment. N Engl J Med. 2025;393(18):1796-1806. doi:10.1056/NEJMoa2511774
14. Alkhezi OS, Alahmed AA, Alfayez OM, Alzuman OA, Almutairi AR, Almohammed OA. Comparative effectiveness of glucagon‐like peptide‐1 receptor agonists for the management of obesity in adults without diabetes: A network meta‐analysis of randomized clinical trials. Obesity Reviews. 2022;24(3). doi:https://doi.org/10.1111/obr.13543
15. Brown JD, Buscemi J, Milsom V, Malcolm R, O’Neil PM. Effects on cardiovascular risk factors of weight losses limited to 5–10 %. Translational Behavioral Medicine. 2015;6(3):339-346. doi:https://doi.org/10.1007/s13142-015-0353-9
16. Ryan DH, Yockey SR. Weight Loss and Improvement in Comorbidity: Differences at 5%, 10%, 15%, and over. Current Obesity Reports. 2017;6(2):187-194. doi:https://doi.org/10.1007/s13679-017-0262-y
17. Look AHEAD Research Group, Gregg EW, Jakicic JM, et al. Association of the magnitude of weight loss and changes in physical fitness with long-term cardiovascular disease outcomes in overweight or obese people with type 2 diabetes: a post-hoc analysis of the Look AHEAD randomised clinical trial. Lancet Diabetes Endocrinol. 2016;4(11):913-921. doi:10.1016/S2213-8587(16)30162-0
18. Yang Y, He L, Han S, et al. Sex Differences in the Efficacy of Glucagon‐Like Peptide‐1 Receptor Agonists for Weight Reduction: A Systematic Review and Meta‐Analysis. Journal of Diabetes. 2025;17(3). doi:https://doi.org/10.1111/1753-0407.70063
19. Gasoyan H, Pfoh ER, Schulte R, Le P, Butsch WS, Rothberg MB. One-Year Weight Reduction With Semaglutide or Liraglutide in Clinical Practice. JAMA Netw Open. 2024;7(9):e2433326. Published 2024 Sep 3. doi:10.1001/jamanetworkopen.2024.33326
20. An X, Sun W, Wen Z, et al. Comparison of the efficacy and safety of GLP-1 receptor agonists on cardiovascular events and risk factors: A review and network meta-analysis. Diabetes Obes Metab. 2025;27(4):1735-1751. doi:10.1111/dom.16228
21. Saldívar-Cerón HI, Vargas-Camacho JA, León-Cabrera S, et al. Oral Small-Molecule GLP-1 Receptor Agonists: Mechanistic Insights and Emerging Therapeutic Strategies. Scientia Pharmaceutica. 2025;93(2):26. doi:https://doi.org/10.3390/scipharm93020026
22. Rosenstock J, Hsia S, Nevarez Ruiz L, et al. Orforglipron, an Oral Small-Molecule GLP-1 Receptor Agonist, in Early Type 2 Diabetes. N Engl J Med. 2025;393(11):1065-1076. doi:10.1056/NEJMoa2505669
23. Rosenstock J, Robins DA, Duffin KL, et al. Orforglipron, an oral non-peptide glucagon-like peptide-1 receptor agonist, improves markers of β-cell function and insulin sensitivity in type 2 diabetes. Diabetes Obes Metab. 2025;27(11):6314-6322. doi:10.1111/dom.70022
24. Rosenstock J, Yabe D, Cox D, et al. Efficacy and safety of once-daily oral orforglipron compared with oral semaglutide in adults with type 2 diabetes (ACHIEVE-3): a multinational, multicentre, non-inferiority, open-label, randomised, phase 3 trial. Lancet. 2026;407(10534):1147-1160. doi:10.1016/S0140-6736(26)00202-3
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Małgorzata Blecharczyk, Aleksandra Jakimowicz, Zuzanna Zofia Kamińska, Aleksandra Malcher, Martyna Mrozek, Martyna Pacanowska-Trawnicka, Agnieszka Zielińska, Igor Zydlewski

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Stats
Number of views and downloads: 30
Number of citations: 0