Evidence map›Paper›PMID 42993255›Full record

ReviewEuropean journal of clinical pharmacology2026

Clinical pharmacology of antidiabetic drugs: an update.

Surasak Wichaiyo

Abstract readReview
PubMed Publisher
In one paragraph

Review in European journal of clinical pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Surasak WichaiyoDepartment of Pharmacology, Faculty of Pharmacy, Mahidol University, 447 Sri-Ayuthaya, Rajathevi, Bangkok, 10400, Thailand. surasak.wic@mahidol.ac.th.ORCID http://orcid.org/0000-0002-1343-7055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis review describes the updated pharmacology of antidiabetic drugs and its translation into clinical applications.

methodsEnglish language literature published from January 1, 1998 to July 25, 2026 was collected using PubMed, ScienceDirect, and Ovid. Research articles, reviews, and clinical practice guidelines were included for discussion.

resultsCurrently, ultra-long-acting basal insulins are emerging, allowing less frequent injections. Glucagon-like peptide 1 receptor agonists (GLP-1RAs), tirzepatide, and sodium-glucose cotransporter-2 inhibitors (SGLT2is) have novel pharmacodynamic properties and clinical evidence of cardiorenal and metabolic benefits, supporting their important roles in individuals with type 2 diabetes (T2D) who have high cardiorenal risk. Because of their effects on weight reduction, GLP-1RAs (semaglutide, liraglutide, and orforglipron) and tirzepatide are approved for the treatment of obesity. Furthermore, SGLT2is (empagliflozin, dapagliflozin, and sotagliflozin) provide cardiorenal benefits, with supporting potential mechanisms, in individuals with heart failure and chronic kidney disease. Conventional oral drugs (e.g., metformin, thiazolidinediones, dipeptidyl peptidase-4 inhibitors, sulfonylureas, meglitinides, and α-glucosidase inhibitors) lack sufficient pharmacologic and clinical data on cardiorenal benefits, suggesting their roles as adjunctive therapies. Novel candidates, including triple incretin hormone agonists (acting on GLP-1, glucose-dependent insulinotropic polypeptide [GIP], and glucagon receptors), GLP-1RA-GIP antagonism-based therapies, amylin analogues, and new dual SGLT1/2 inhibitors, show promising results for glycemic control and weight loss.

conclusionOverall, a comprehensive understanding of the pharmacologic characteristics of antidiabetic drugs promotes appropriate drug use for the management of T2D and cardiometabolic diseases and helps avoid undesirable events. Ongoing investigations of novel approaches may contribute to improved patient care in the future.

Indexed as

Diabetes Mellitus, Type 2Hypoglycemic AgentsGlucagon-Like Peptide-1 Receptor AgonistsHumansSodium-Glucose Transporter 2 InhibitorsTirzepatideGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsTirzepatideAntidiabeticsCardiovascular diseasesChronic kidney diseaseMetabolic disordersPharmacologyType 2 diabetes

Identifiers

PMID42993255

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.