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September 14, 2025105 citations

Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity.

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SWSean WhartonILIldiko LingvayPBPaweł Bogdański

Key Points

  • Oral semaglutide resulted in a mean weight reduction of -13.6%, compared to -2.2% with placebo over 64 weeks.
  • Participants receiving oral semaglutide were more likely to achieve weight loss of 5% or more, with significant differences (P<0.001).
  • The double-blind, randomized, placebo-controlled trial enrolled 307 adults with obesity across four countries.
  • Gastrointestinal adverse events were more frequent in the oral semaglutide group (74%) compared to placebo (42.2%).

Abstract

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. 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. 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%). 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.).

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Cite This Study

Wharton et al. (2025) studied this question.

synapsesocial.com/papers/68c6df6de03a6c7bdc170f74https://doi.org/10.1056/nejmoa2500969
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