Table 3.
Clinical studies of GLP1RAs for the treatment of DM or DM-related diseases
| Medicine | Generic Name | First Author | Year | Disease | Model | Findings | Ref. |
|---|---|---|---|---|---|---|---|
| GLP1RAs | Dulaglutide | Gerstein, H.C. | 2020 | T2DM | Human | Long-term dulaglutide use might reduce clinically relevant ischemic stroke in people with T2DM | [127] |
| Tuttolomondo, A. | 2021 | T2DM | Human | Positive effects on arterial stiffness and endothelial function indicators in patients with T2DM receiving conventional therapy with daily subcutaneous injections of 1.5 mg dulaglutide | [128] | ||
| Liraglutide | Marso, S.P. | 2016 | T2DM | Human | The composite endpoint of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke was significantly lower in T2DM patients at high cardiovascular risk | [129] | |
| Semaglutide | Husain, M. | 2019 | T2DM | Human | The cardiovascular risk profile of patients with T2DM taking oral semaglutide was not worse than those taking placebo | [130] | |
| Strain, W.D. | 2022 | T2DM | Human | Semaglutide treatment reduced stroke risk in patients with T2DM and higher cardiovascular risk compared with placebo treatment | [131] | ||
| Efpeglenatide | Gerstein, H.C. | 2021 | T2DM | Human | Patients with T2DM who received weekly subcutaneous doses of 4 or 6 mg of efpeglenatide had a lower risk of cardiovascular events than those on placebo | [132] | |
| Albiglutide | Hernandez, A.F. | 2018 | T2DM | Human | In patients with T2DM and cardiovascular disease, albiglutide was superior to placebo with respect to major adverse cardiovascular events | [133] |