Sean Wharton,Ildiko Lingvay,Pawel Bogdanski,Ruben Duque do Vale,Stephan Jacob,Tobias Karlsson,Chaithra Shaji,Domenica Rubino,W Timothy Garvey,
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The coprimary end points at week 64 were the percent change in body weight and a reduction of 5% or more in body weight; confirmatory secondary end points included reductions in body weight of 10% or more, 15% or more, and 20% or more and the change in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function score.\r\n\r\nRESULTS\r\nA total of 205 participants were randomly assigned to receive oral semaglutide, and 102 to receive placebo. The estimated mean change in body weight from baseline to week 64 was -13.6% in the oral semaglutide group and -2.2% in the placebo group (estimated difference, -11.4 percentage points; 95% confidence interval, -13.9 to -9.0; P<0.001). Participants in the oral semaglutide group were significantly more likely than those in the placebo group to have body-weight reductions of 5% or more, 10% or more, 15% or more, and 20% or more (P<0.001 for all comparisons) and to have an improved IWQOL-Lite-CT Physical Function score (P<0.001). Gastrointestinal adverse events were more common with oral semaglutide than with placebo (74.0% vs. 42.2%).\r\n\r\nCONCLUSIONS\r\nOral semaglutide at a dose of 25 mg once daily resulted in a greater mean reduction in body weight than placebo in participants with overweight or obesity. 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The participants were randomly assigned in a 2:1 ratio to receive oral semaglutide (25 mg) or placebo once daily, plus lifestyle interventions. The coprimary end points at week 64 were the percent change in body weight and a reduction of 5% or more in body weight; confirmatory secondary end points included reductions in body weight of 10% or more, 15% or more, and 20% or more and the change in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function score.\\r\\n\\r\\nRESULTS\\r\\nA total of 205 participants were randomly assigned to receive oral semaglutide, and 102 to receive placebo. The estimated mean change in body weight from baseline to week 64 was -13.6% in the oral semaglutide group and -2.2% in the placebo group (estimated difference, -11.4 percentage points; 95% confidence interval, -13.9 to -9.0; P<0.001). 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引用次数: 0
摘要
背景:对于超重或肥胖的人来说,口服25毫克的西马鲁肽可能是注射西马鲁肽(2.4毫克)和高剂量口服西马鲁肽(50毫克)的替代治疗选择。方法:在一项为期71周的双盲、随机、安慰剂对照试验中,我们在4个国家的22个地点进行了研究,招募了身体质量指数(BMI,体重公斤除以身高米的平方)为30或更高或BMI为27或更高且至少有一种肥胖相关并发症的无糖尿病患者。参与者以2:1的比例随机分配,每天一次口服西马鲁肽(25mg)或安慰剂,外加生活方式干预。第64周的主要终点是体重变化百分比和体重减少5%或更多;确定的次要终点包括体重减少10%或更多、15%或更多、20%或更多,以及体重对生命质量临床试验版本(iwqol - life - ct)身体功能评分的影响。结果共205名受试者被随机分配接受口服西马鲁肽治疗,102名受试者接受安慰剂治疗。口服西马鲁肽组从基线到第64周体重的估计平均变化为-13.6%,安慰剂组为-2.2%(估计差异为-11.4个百分点;95%可信区间为-13.9至-9.0;P<0.001)。与安慰剂组相比,口服西马鲁肽组的受试者体重减轻5%或更多、10%或更多、15%或更多和20%或更多的可能性显著增加(所有比较的P<0.001), IWQOL-Lite-CT身体功能评分也有改善(P<0.001)。胃肠道不良事件在口服西马鲁肽组比安慰剂组更常见(74.0% vs 42.2%)。结论:在超重或肥胖的参与者中,口服西马鲁肽25 mg,每日一次,比安慰剂更能降低体重。(由诺和诺德资助;OASIS 4 ClinicalTrials.gov号码,NCT05564117.)。
Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity.
BACKGROUND
Oral semaglutide at a dose of 25 mg may provide an alternative treatment option to injectable semaglutide (2.4 mg) and higher-dose oral semaglutide (50 mg) for persons with overweight or obesity.
METHODS
In a 71-week, double-blind, randomized, placebo-controlled trial conducted at 22 sites in four countries, we enrolled persons without diabetes who had a body-mass index (BMI; the weight in kilograms divided by the square of the height in meters) of 30 or higher or a BMI of 27 or higher with at least one obesity-related complication. The participants were randomly assigned in a 2:1 ratio to receive oral semaglutide (25 mg) or placebo once daily, plus lifestyle interventions. The coprimary end points at week 64 were the percent change in body weight and a reduction of 5% or more in body weight; confirmatory secondary end points included reductions in body weight of 10% or more, 15% or more, and 20% or more and the change in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function score.
RESULTS
A total of 205 participants were randomly assigned to receive oral semaglutide, and 102 to receive placebo. The estimated mean change in body weight from baseline to week 64 was -13.6% in the oral semaglutide group and -2.2% in the placebo group (estimated difference, -11.4 percentage points; 95% confidence interval, -13.9 to -9.0; P<0.001). Participants in the oral semaglutide group were significantly more likely than those in the placebo group to have body-weight reductions of 5% or more, 10% or more, 15% or more, and 20% or more (P<0.001 for all comparisons) and to have an improved IWQOL-Lite-CT Physical Function score (P<0.001). Gastrointestinal adverse events were more common with oral semaglutide than with placebo (74.0% vs. 42.2%).
CONCLUSIONS
Oral semaglutide at a dose of 25 mg once daily resulted in a greater mean reduction in body weight than placebo in participants with overweight or obesity. (Funded by Novo Nordisk; OASIS 4 ClinicalTrials.gov number, NCT05564117.).
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.