Future Medications for Obesity and Clinical Implications.
Diabetes Spectr · 2024
Last updated 2026-05-28Two recently approved drugs for obesity, semaglutide and tirzepatide, helped participants lose at least 15% of their body weight in clinical trials. Other medications in development target similar hormone pathways and may also improve obesity-related health problems like blood sugar control and heart disease.
AI summary of the abstract below.
| Journal | Diabetes Spectr, 2024 |
|---|---|
| Citations | 3 |
| Relative citation ratio | 0.61 |
| NIH percentile | 35 |
| Molecules | — |
| Conditions studied | Obesity |
Abstract
Semaglutide and tirzepatide have recently been approved for obesity and found to achieve ≥15% weight loss in clinical trials. These drugs have been referred to as second-generation medications because the unprecedented degree of weight loss they afford is sufficient to treat or prevent a broad array of obesity complications and related diseases. Many other medications are in development based on the actions of nutrient-regulated hormones (NRHs), including mono-, dual-, and triple-receptor agonists/antagonists for glucagon-like peptide 1, glucose-dependent insulinotropic polypeptide, amylin, peptide tyrosine-tyrosine, and glucagon. Clinical trial evidence is accumulating that these medications ameliorate multiple biomechanical, metabolic, and vascular complications of obesity. These tools enable a comprehensive complications-centric approach to care within the contextual framework of the diagnostic term adiposity-based chronic disease (ABCD). The potential to reduce patient suffering and the huge social burden of ABCD is profound. The current era of drug development based on NRHs could represent a landmark in the history of medicine provided that societies ensure access to these medications for the patients who need them.
Verbatim abstract via PubMed 39649698 ↗