open access publication

Article, Early Access, 2024

Real-World Use of Oral Semaglutide in Adults with Type 2 Diabetes in the PIONEER REAL Netherlands Multicentre, Prospective, Observational Study

DIABETES THERAPY, ISSN 1869-6953, 1869-6953, 10.1007/s13300-024-01588-5

Contributors

van Houtum, William (Corresponding author) [1] Schrombges, Patrick [2] Amadid, Hanan [3] van Bon, Arianne C. [4] Braae, Uffe Christian 0000-0002-2743-4584 [3] Hoogstraten, Charlotte [5] Herrings, Hans [6]

Affiliations

  1. [1] Spaarne Gasthuis, Dept Internal Med, Spaarnepoort 1, NL-2134 TM Hoofddorp, Netherlands
  2. [NORA names: Netherlands; Europe, EU; OECD];
  3. [2] Tunnis Huisartsen, Sint Anthonis, Netherlands
  4. [NORA names: Netherlands; Europe, EU; OECD];
  5. [3] Novo Nordisk AS, Soborg, Denmark
  6. [NORA names: Novo Nordisk; Private Research; Denmark; Europe, EU; Nordic; OECD];
  7. [4] Rijnstate Dept Internal Med, Arnhem, Netherlands
  8. [NORA names: Netherlands; Europe, EU; OECD];
  9. [5] Novo Nordisk AS, Alphen Aan Den Rijn, Netherlands
  10. [NORA names: Netherlands; Europe, EU; OECD];

Abstract

Introduction: In this phase 4, multicentre, prospective, non-interventional PIONEER REAL Netherlands study, we assessed clinical outcomes associated with once-daily oral semaglutide use in real-world clinical practice in adults living with type 2 diabetes (T2D) na & iuml;ve to injectable glucose-lowering medication. Methods: Participants initiated on oral semaglutide were followed for 34-44 weeks. Change in glycated haemoglobin (HbA1c) from baseline (BL) to end of study (EOS) was the primary endpoint; secondary endpoints included change in body weight (BW) from BL to EOS, the proportion of participants with HbA1c < 7.0% at EOS and the composite endpoints of HbA1c reduction >= 1.0%-points with BW reduction >= 3% or >= 5% at EOS. Treatment satisfaction was assessed using the Diabetes Treatment Satisfaction Questionnaire (DTSQ status/change). Safety was evaluated in all participants who initiated oral semaglutide treatment. Results: Oral semaglutide was initiated in 187 participants; 94.1% completed the study and 78.6% remained on treatment at EOS. At BL, 54.0% of participants were male, mean age was 58.8 years, mean duration of T2D was 8.7 years and mean body mass index was 35.1 kg/m(2); mean HbA1c was 8.6% and mean BW was 103.1 kg. Significant improvements from BL to EOS were observed for HbA1c and BW (estimated change [95% confidence interval]: - 1.16%-points [- 1.48 to - 0.85]; p < 0.0001, and - 5.84 kg [- 6.88 to - 4.80]; p < 0.0001, respectively). At EOS, 47.5% of participants had an HbA1c level < 7.0%; 41.8% and 35.5% of participants achieved composite endpoints of HbA1c reduction >= 1.0%-points plus BW reduction >= 3% or >= 5%, respectively. DTSQ status and change scores improved by 2.1 (p = 0.0003) and 10.8 points (p < 0.0001), respectively. Oral semaglutide was easy or very easy to consume for 81.5% of participants. Adverse events were mostly mild/moderate, with gastrointestinal disorders being the most common. Conclusion: In this real-world population, we reported clinically significant reductions in HbA1c and BW, improved treatment satisfaction and no new safety concerns.

Keywords

Body weight, GLP-1 receptor agonist, Glycaemic control, HbA1c, Incretin therapy, Real-world evidence, Semaglutide, Type 2 diabetes

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