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      Continued Treatment With Tirzepatide for Maintenance of Weight Reduction in Adults With Obesity : The SURMOUNT-4 Randomized Clinical Trial

      1 , 2 , 3 , 4 , 5 , 6 , 7 , 7 , 7 , 7 , 8 , 7 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , 9 , SURMOUNT-4 Investigators
      JAMA
      American Medical Association (AMA)

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          Abstract

          Importance

          The effect of continued treatment with tirzepatide on maintaining initial weight reduction is unknown.

          Objective

          To assess the effect of tirzepatide, with diet and physical activity, on the maintenance of weight reduction.

          Design, Setting, and Participants

          This phase 3, randomized withdrawal clinical trial conducted at 70 sites in 4 countries with a 36-week, open-label tirzepatide lead-in period followed by a 52-week, double-blind, placebo-controlled period included adults with a body mass index greater than or equal to 30 or greater than or equal to 27 and a weight-related complication, excluding diabetes.

          Interventions

          Participants (n = 783) enrolled in an open-label lead-in period received once-weekly subcutaneous maximum tolerated dose (10 or 15 mg) of tirzepatide for 36 weeks. At week 36, a total of 670 participants were randomized (1:1) to continue receiving tirzepatide (n = 335) or switch to placebo (n = 335) for 52 weeks.

          Main Outcomes and Measures

          The primary end point was the mean percent change in weight from week 36 (randomization) to week 88. Key secondary end points included the proportion of participants at week 88 who maintained at least 80% of the weight loss during the lead-in period.

          Results

          Participants (n = 670; mean age, 48 years; 473 [71%] women; mean weight, 107.3 kg) who completed the 36-week lead-in period experienced a mean weight reduction of 20.9%. The mean percent weight change from week 36 to week 88 was −5.5% with tirzepatide vs 14.0% with placebo (difference, −19.4% [95% CI, −21.2% to −17.7%]; P < .001). Overall, 300 participants (89.5%) receiving tirzepatide at 88 weeks maintained at least 80% of the weight loss during the lead-in period compared with 16.6% receiving placebo ( P < .001). The overall mean weight reduction from week 0 to 88 was 25.3% for tirzepatide and 9.9% for placebo. The most common adverse events were mostly mild to moderate gastrointestinal events, which occurred more commonly with tirzepatide vs placebo.

          Conclusions and Relevance

          In participants with obesity or overweight, withdrawing tirzepatide led to substantial regain of lost weight, whereas continued treatment maintained and augmented initial weight reduction.

          Trial Registration

          ClinicalTrials.gov Identifier: NCT04660643

          Related collections

          Most cited references31

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          Once-Weekly Semaglutide in Adults with Overweight or Obesity

          Obesity is a global health challenge with few pharmacologic options. Whether adults with obesity can achieve weight loss with once-weekly semaglutide at a dose of 2.4 mg as an adjunct to lifestyle intervention has not been confirmed.
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            A Randomized, Controlled Trial of 3.0 mg of Liraglutide in Weight Management.

            Obesity is a chronic disease with serious health consequences, but weight loss is difficult to maintain through lifestyle intervention alone. Liraglutide, a glucagon-like peptide-1 analogue, has been shown to have potential benefit for weight management at a once-daily dose of 3.0 mg, injected subcutaneously.
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              Tirzepatide Once Weekly for the Treatment of Obesity

              Obesity is a chronic disease that results in substantial global morbidity and mortality. The efficacy and safety of tirzepatide, a novel glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist, in people with obesity are not known.
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                Author and article information

                Journal
                JAMA
                JAMA
                American Medical Association (AMA)
                0098-7484
                December 11 2023
                Affiliations
                [1 ]Comprehensive Weight Control Center, Division of Endocrinology, Diabetes, and Metabolism, Weill Cornell Medicine, New York, New York
                [2 ]BHF Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom
                [3 ]University of Texas Center for Obesity Medicine and Metabolic Performance, Department of Surgery, University of Texas McGovern Medical School, Houston
                [4 ]Louisville Metabolic and Atherosclerosis Research Center, Louisville, Kentucky
                [5 ]McMaster University, and Wharton Weight Management Clinic, York University, Toronto, Ontario, Canada
                [6 ]Department of Family Medicine, China Medical University Hospital, Taichung, Taiwan
                [7 ]Eli Lilly and Company, Indianapolis, Indiana
                [8 ]Eli Lilly and Company, Moscow, Russia
                [9 ]for the SURMOUNT-4 Investigators
                Article
                10.1001/jama.2023.24945
                38078870
                7fa4f1a6-469f-4d2f-beef-f7cb664ebc78
                © 2023
                History

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