Tirzepatide as Compared with Semaglutide for the Treatment of Obesity.

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Louis J Aronne,Deborah Bade Horn,Carel W le Roux,Wayne Ho,Beverly L Falcon,Elisa Gomez Valderas,Sagar Das,Clare J Lee,Leonard C Glass,Cagri Senyucel,Julia P Dunn,
{"title":"Tirzepatide as Compared with Semaglutide for the Treatment of Obesity.","authors":"Louis J Aronne,Deborah Bade Horn,Carel W le Roux,Wayne Ho,Beverly L Falcon,Elisa Gomez Valderas,Sagar Das,Clare J Lee,Leonard C Glass,Cagri Senyucel,Julia P Dunn,","doi":"10.1056/nejmoa2416394","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nTirzepatide and semaglutide are highly effective medications for obesity management. The efficacy and safety of tirzepatide as compared with semaglutide in adults with obesity but without type 2 diabetes is unknown.\r\n\r\nMETHODS\r\nIn this phase 3b, open-label, controlled trial, adult participants with obesity but without type 2 diabetes were randomly assigned in a 1:1 ratio to receive the maximum tolerated dose of tirzepatide (10 mg or 15 mg) or the maximum tolerated dose of semaglutide (1.7 mg or 2.4 mg) subcutaneously once weekly for 72 weeks. The primary end point was the percent change in weight from baseline to week 72. Key secondary end points included weight reductions of at least 10%, 15%, 20%, and 25% and a change in waist circumference from baseline to week 72.\r\n\r\nRESULTS\r\nA total of 751 participants underwent randomization. The least-squares mean percent change in weight at week 72 was -20.2% (95% confidence interval [CI], -21.4 to -19.1) with tirzepatide and -13.7% (95% CI, -14.9 to -12.6) with semaglutide (P<0.001). The least-squares mean change in waist circumference was -18.4 cm (95% CI, -19.6 to -17.2) with tirzepatide and -13.0 cm (95% CI, -14.3 to -11.7) with semaglutide (P<0.001). Participants in the tirzepatide group were more likely than those in the semaglutide group to have weight reductions of at least 10%, 15%, 20%, and 25%. The most common adverse events in both treatment groups were gastrointestinal, and most were mild to moderate in severity and occurred primarily during dose escalation.\r\n\r\nCONCLUSIONS\r\nAmong participants with obesity but without diabetes, treatment with tirzepatide was superior to treatment with semaglutide with respect to reduction in body weight and waist circumference at week 72. (Funded by Eli Lilly; SURMOUNT-5 ClinicalTrials.gov number, NCT05822830.).","PeriodicalId":54725,"journal":{"name":"New England Journal of Medicine","volume":"44 1","pages":""},"PeriodicalIF":96.2000,"publicationDate":"2025-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New England Journal of Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1056/nejmoa2416394","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND Tirzepatide and semaglutide are highly effective medications for obesity management. The efficacy and safety of tirzepatide as compared with semaglutide in adults with obesity but without type 2 diabetes is unknown. METHODS In this phase 3b, open-label, controlled trial, adult participants with obesity but without type 2 diabetes were randomly assigned in a 1:1 ratio to receive the maximum tolerated dose of tirzepatide (10 mg or 15 mg) or the maximum tolerated dose of semaglutide (1.7 mg or 2.4 mg) subcutaneously once weekly for 72 weeks. The primary end point was the percent change in weight from baseline to week 72. Key secondary end points included weight reductions of at least 10%, 15%, 20%, and 25% and a change in waist circumference from baseline to week 72. RESULTS A total of 751 participants underwent randomization. The least-squares mean percent change in weight at week 72 was -20.2% (95% confidence interval [CI], -21.4 to -19.1) with tirzepatide and -13.7% (95% CI, -14.9 to -12.6) with semaglutide (P<0.001). The least-squares mean change in waist circumference was -18.4 cm (95% CI, -19.6 to -17.2) with tirzepatide and -13.0 cm (95% CI, -14.3 to -11.7) with semaglutide (P<0.001). Participants in the tirzepatide group were more likely than those in the semaglutide group to have weight reductions of at least 10%, 15%, 20%, and 25%. The most common adverse events in both treatment groups were gastrointestinal, and most were mild to moderate in severity and occurred primarily during dose escalation. CONCLUSIONS Among participants with obesity but without diabetes, treatment with tirzepatide was superior to treatment with semaglutide with respect to reduction in body weight and waist circumference at week 72. (Funded by Eli Lilly; SURMOUNT-5 ClinicalTrials.gov number, NCT05822830.).
替西帕肽与西马鲁肽治疗肥胖症的比较。
背景:替西帕肽和西马鲁肽是治疗肥胖非常有效的药物。与西马鲁肽相比,替西帕肽在成人肥胖但无2型糖尿病患者中的疗效和安全性尚不清楚。方法:在这项3b期、开放标签、对照试验中,肥胖但无2型糖尿病的成年受试者按1:1的比例随机分配,接受最大耐受剂量的替西帕肽(10mg或15mg)或最大耐受剂量的西马鲁肽(1.7 mg或2.4 mg),每周皮下注射一次,持续72周。主要终点是从基线到第72周体重变化的百分比。关键的次要终点包括体重减轻至少10%、15%、20%和25%,以及从基线到第72周腰围的变化。结果共751名受试者被随机分组。第72周时,替西帕肽组体重变化的最小二乘平均值为-20.2%(95%可信区间[CI], -21.4至-19.1),西马鲁肽组为-13.7% (95% CI, -14.9至-12.6)(P<0.001)。替西帕肽组腰围的最小二乘平均变化为-18.4 cm (95% CI, -19.6至-17.2),西马鲁肽组腰围的最小二乘平均变化为-13.0 cm (95% CI, -14.3至-11.7)(P<0.001)。替西帕肽组的参与者比西马鲁肽组的参与者更有可能体重减轻至少10%,15%,20%和25%。两个治疗组中最常见的不良事件是胃肠道,大多数严重程度为轻度至中度,主要发生在剂量增加期间。结论:在肥胖但无糖尿病的受试者中,在72周体重和腰围的降低方面,替西帕肽治疗优于西马鲁肽治疗。(由礼来公司资助;SURMOUNT-5 ClinicalTrials.gov编号:NCT05822830)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信