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[Anti-obesity drugs : from previous disappointments to new hopes].

Rev Med Liege · 2023

Last updated 2026-05-28

Most older anti-obesity drugs were withdrawn due to serious side effects like heart and brain risks. Newer drugs, such as GLP-1 receptor agonists like liraglutide and semaglutide, originally used for diabetes, are now prescribed at higher doses for weight loss. A newer drug called tirzepatide, which targets both GLP-1 and GIP receptors, is being tested and appears to be more effective for lowering blood sugar and aiding weight loss.

AI summary of the abstract below.

JournalRev Med Liege, 2023
Citations3
Relative citation ratio0.47
NIH percentile27
Molecules
Conditions studied Obesity

Abstract

Both physicians and patients dream of an efficacious and safe pharmacological approach to treat obesity. Unfortunately, most anti-obesity drugs prescribed since the fifties were associated with an unfavourable risk profile that led to numerous withdrawals. Medications issued from pharmaco-chemistry that mainly target brain amines to reduce appetite have been abandoned because of potential cardiovascular and neuropsychiatric toxicities. More recently, biological medications emerged, especially GLP-1 (Glucagon-Like Peptide-1) receptor agonists, well-known to manage type 2 diabetes and now recommended at higher doses for the treatment of obesity (liraglutide, semaglutide). A dual agonist that targets both GLP-1 and GIP (Glucose-dependent Insulinotropic Polypeptide) receptors (tirzepatide) appears to be even more potent as glucose-lowering agent and is currently tested as an anti-obesity agent. Many other pharmacological approaches are currently investigated but they should not mask the importance of life-style measurements.

Verbatim abstract via PubMed 36924152 ↗