Use of once‐daily oral semaglutide and associated clinical outcomes among adults with type 2 diabetes in routine clinical practice in Canada: A multicentre, prospective real‐world study (PIONEER REAL Canada)

Author:

Jain Akshay B.12ORCID,Reichert Sonja M.3,Amadid Hanan4,Braae Uffe C.4,Bradley Ryan M.5,Kim James W.6,Soo Victoria7,Yale Jean‐François8ORCID

Affiliation:

1. TLC Diabetes and Endocrinology Surrey Canada

2. Division of Endocrinology and Metabolism University of British Columbia Vancouver Canada

3. Department of Family Medicine and Centre for Studies in Family Medicine, Schulich School of Medicine & Dentistry Western University London Canada

4. Novo Nordisk A/S Søborg Denmark

5. Novo Nordisk Inc. Mississauga Canada

6. Department of Family Medicine University of Calgary Calgary Canada

7. Department of Family Medicine Western University London Canada

8. Division of Endocrinology and Metabolism, Department of Medicine McGill University Montréal Canada

Abstract

AbstractAimPIONEER REAL Canada examined real‐world clinical outcomes associated with the use of once‐daily oral semaglutide in adults with type 2 diabetes.Materials and MethodsThis was a 34‐ to 44‐week, multicentre, prospective, open‐label, non‐interventional study in adults who were treatment‐naive to injectable glucose‐lowering medication and initiated oral semaglutide in routine clinical practice. The primary endpoint was the change in glycated haemoglobin (HbA1c) from baseline to the end of the study (EoS). Secondary endpoints assessed at EoS were change from baseline in body weight (BW); the proportion of participants reaching HbA1c levels <7% and the composite endpoints, HbA1c reduction ≥1% point with BW reduction ≥3% and ≥5%; and treatment satisfaction measured using Diabetes Treatment Satisfaction Questionnaires (DTSQ) status and change. Primary analyses were based on the in‐study observation period.ResultsIn total, 182 participants initiated oral semaglutide (mean age, 58.6 years; HbA1c, 8.0%; BW, 93.7 kg). The estimated changes (95% confidence interval) from baseline to EoS in HbA1c and BW were −1.09% points (−1.24, −0.94; p < .0001) and −7.17% (−8.24, −6.11; p < .0001), respectively. At EoS, 53.7% of participants had HbA1c levels <7%; 39.3% and 31.6% reached HbA1c reduction ≥1% point plus BW reduction ≥3% and ≥5%, respectively. Treatment satisfaction significantly increased (DTSQ status, +4.47 points; DTSQ change, 11.83 points; both p < .0001). At EoS, 75.3% of participants remained on oral semaglutide (55.5% received oral semaglutide 14 mg). No new safety signals were identified for oral semaglutide.ConclusionsIn PIONEER REAL Canada, participants treated with oral semaglutide in routine clinical practice experienced clinically relevant reductions in HbA1c and BW and increased treatment satisfaction.

Funder

Novo Nordisk Pharma

Publisher

Wiley

Reference21 articles.

1. Management of hyperglycaemia in type 2 diabetes, 2022. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)

2. Pharmacologic Glycemic Management of Type 2 Diabetes in Adults: 2020 Update

3. Preference for Type 2 Diabetes Therapies in the United States: A Discrete Choice Experiment

4. European Medicines Agency. Ozempic® (semaglutide) injection: summary of product characteristics.2022;https://www.ema.europa.eu/en/documents/product‐information/ozempic‐epar‐product‐information_en.pdf. Accessed March 15 2023.

5. US Food and Drug Administration. Ozempic® (semaglutide) injection: prescribing information.2020;https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209637s003lbl.pdf. Accessed March 15 2023.

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