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Future Medications for Obesity and Clinical Implications.

Diabetes Spectr · 2024

Last updated 2026-05-28

Two 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.

JournalDiabetes Spectr, 2024
Citations3
Relative citation ratio0.61
NIH percentile35
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 ↗