Semaglutide 2.4 mg for the Treatment of Obesity: Key Elements of the STEP Trials 1 to 5

  • Robert F. Kushner
    Division of Endocrinology Feinberg School of Medicine Northwestern University Chicago Illinois USA
  • Salvatore Calanna
    Novo Nordisk A/S Søborg Denmark
  • Melanie Davies
    Diabetes Research Centre University of Leicester Leicester UK
  • Dror Dicker
    Department of Internal Medicine Hasharon Hospital Rabin Medical Center Petah Tikva Israel
  • W. Timothy Garvey
    Department of Nutrition Sciences University of Alabama at Birmingham Birmingham Alabama USA
  • Bryan Goldman
    Novo Nordisk A/S Søborg Denmark
  • Ildiko Lingvay
    Department of Internal Medicine/Endocrinology UT Southwestern Medical Center Dallas Texas USA
  • Mette Thomsen
    Novo Nordisk A/S Søborg Denmark
  • Thomas A. Wadden
    Department of Psychiatry Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA
  • Sean Wharton
    York University and Wharton Weight Management Clinic Toronto Ontario Canada
  • John P.H. Wilding
    Obesity and Endocrinology Research Institute of Ageing and Chronic Disease University of Liverpool Liverpool UK
  • Domenica Rubino
    Washington Center for Weight Management and Research Arlington Virginia USA

説明

<jats:sec><jats:title>Objective</jats:title><jats:p>The obesity epidemic is a public health concern, warranting further research into pharmacological treatments for weight management (WM) as an adjunct to lifestyle interventions. The Semaglutide Treatment Effect in People with obesity (STEP) program aims to investigate the effect of semaglutide versus placebo on weight loss, safety, and tolerability in adults with obesity or overweight.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Across five phase 3 trials (NCT03548935, WM; NCT03552757, WM in type 2 diabetes; NCT03611582, WM with intensive behavioral therapy; NCT03548987, sustained WM; and NCT03693430, long‐term WM), ~5,000 participants are being randomly assigned to receive semaglutide 2.4 mg once weekly subcutaneously versus placebo. Results will be available in 2020/2021. For all trials, the primary end point is change from baseline to end of treatment in body weight.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Participants have a mean age of 46.2 to 55.3 years, are mostly female (mean: 74.1%‐81.0%), and have a mean BMI of 35.7 to 38.5 kg/m<jats:sup>2</jats:sup> and a mean waist circumference of 113.0 to 115.7 cm.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>The STEP program evaluates the efficacy and safety of semaglutide 2.4 mg subcutaneously once weekly in a broad population. The trials will provide insights on WM in people with obesity with and without type 2 diabetes and on long‐term follow‐up.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/oby22794-fig-0006-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p></jats:sec>

収録刊行物

  • Obesity

    Obesity 28 (6), 1050-1061, 2020-05-22

    Wiley

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