Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?

There is a new generation of antiobesity drugs in development or just arriving on the scene. First, setmelanotide has been approved for three of the ultrarare genetic conditions that cause obesity–#8211;pro-opiomelanocortin deficiency, proprotein convertase subtilisin and kexin type 1 (an important...

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Main Author: Donna H. Ryan
Format: Article
Language:English
Published: Korean Society for the Study of Obesity 2021-09-01
Series:Journal of Obesity & Metabolic Syndrome
Subjects:
Online Access:http://journaleditor.inforang.com/journal/view.html?doi=10.7570/jomes21033
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spelling doaj-22b9f4bf26bd49b59dbad1b4b65e8c972021-09-30T07:52:31ZengKorean Society for the Study of ObesityJournal of Obesity & Metabolic Syndrome2508-62352021-09-0130319620810.7570/jomes21033jomes21033Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?Donna H. Ryan0Pennington Biomedical Research Center, Baton Rouge, LA, USAThere is a new generation of antiobesity drugs in development or just arriving on the scene. First, setmelanotide has been approved for three of the ultrarare genetic conditions that cause obesity–#8211;pro-opiomelanocortin deficiency, proprotein convertase subtilisin and kexin type 1 (an important enzyme in the melanocortin pathway) and leptin receptor deficiency. Setmelanotide marks the first in a personalized medicine approach to obesity. Second, semaglutide 2.4 mg once weekly has been submitted to regulators in the United States and the European Union for approval for patients with obesity (body mass index [BMI] –#8805;30 kg/m2) or overweight (BMI –#8805;27 kg/m2) and at least one weight related comorbidity. This drug has been studied in five phase 3 clinical trials, four discussed herein: semaglutide produces roughly twice as much weight loss as we have seen in older antiobesity medications. Semaglutide is already in use for treatment of diabetes and, as a glucagon-like peptide 1 (GLP-1) receptor analog, is part of a class of drugs used widely in diabetes. Tirzepatide, a glucose-insulin peptide and GLP-1 dual agonist is in phase 3 study for obesity management, and bimagrumab is a new agent in phase 2 with a unique mechanism of action; they are generating much interest. The purpose of this narrative review is lay the groundwork for a discussion of the clinical impact of these new medications on the clinical practice of obesity. Further, these developments shall be used to launch a speculation of what is likely to be their impact on the future of obesity pharmacotherapy.http://journaleditor.inforang.com/journal/view.html?doi=10.7570/jomes21033anti-obesity agentsanti-obesity drugsweight loss agentssetmelanotidesemaglutidetirzepatidebimagrumab
collection DOAJ
language English
format Article
sources DOAJ
author Donna H. Ryan
spellingShingle Donna H. Ryan
Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
Journal of Obesity & Metabolic Syndrome
anti-obesity agents
anti-obesity drugs
weight loss agents
setmelanotide
semaglutide
tirzepatide
bimagrumab
author_facet Donna H. Ryan
author_sort Donna H. Ryan
title Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
title_short Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
title_full Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
title_fullStr Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
title_full_unstemmed Next Generation Antiobesity Medications: Setmelanotide, Semaglutide, Tirzepatide and Bimagrumab: What do They Mean for Clinical Practice?
title_sort next generation antiobesity medications: setmelanotide, semaglutide, tirzepatide and bimagrumab: what do they mean for clinical practice?
publisher Korean Society for the Study of Obesity
series Journal of Obesity & Metabolic Syndrome
issn 2508-6235
publishDate 2021-09-01
description There is a new generation of antiobesity drugs in development or just arriving on the scene. First, setmelanotide has been approved for three of the ultrarare genetic conditions that cause obesity–#8211;pro-opiomelanocortin deficiency, proprotein convertase subtilisin and kexin type 1 (an important enzyme in the melanocortin pathway) and leptin receptor deficiency. Setmelanotide marks the first in a personalized medicine approach to obesity. Second, semaglutide 2.4 mg once weekly has been submitted to regulators in the United States and the European Union for approval for patients with obesity (body mass index [BMI] –#8805;30 kg/m2) or overweight (BMI –#8805;27 kg/m2) and at least one weight related comorbidity. This drug has been studied in five phase 3 clinical trials, four discussed herein: semaglutide produces roughly twice as much weight loss as we have seen in older antiobesity medications. Semaglutide is already in use for treatment of diabetes and, as a glucagon-like peptide 1 (GLP-1) receptor analog, is part of a class of drugs used widely in diabetes. Tirzepatide, a glucose-insulin peptide and GLP-1 dual agonist is in phase 3 study for obesity management, and bimagrumab is a new agent in phase 2 with a unique mechanism of action; they are generating much interest. The purpose of this narrative review is lay the groundwork for a discussion of the clinical impact of these new medications on the clinical practice of obesity. Further, these developments shall be used to launch a speculation of what is likely to be their impact on the future of obesity pharmacotherapy.
topic anti-obesity agents
anti-obesity drugs
weight loss agents
setmelanotide
semaglutide
tirzepatide
bimagrumab
url http://journaleditor.inforang.com/journal/view.html?doi=10.7570/jomes21033
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