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Real-World Use of Once-Weekly Semaglutide in Type 2 Diabetes: Results from the SURE UK Multicentre, Prospective, Observational Study

Holmes, Patrick; Bell, Heather Elizabeth; Bozkurt, Karan; Catarig, Andrei Mircea; Clark, Alice; Machell, Alena; Sathyapalan, Thozhukat

Authors

Patrick Holmes

Heather Elizabeth Bell

Karan Bozkurt

Andrei Mircea Catarig

Alice Clark

Alena Machell



Abstract

Introduction: Once-weekly (OW) semaglutide was associated with clinically relevant improvements in glycaemic control and body weight versus comparators in the SUSTAIN randomised controlled trials (RCTs). SURE UK, which is one of a series of individual studies that comprise the SURE programme, evaluated the use of OW semaglutide in a real-world patient population with type 2 diabetes (T2D) in the UK. Methods: In this prospective, observational study, adults (≥ 18years) with ≥ 1 documented glycated haemoglobin (HbA1c) value ≤ 12weeks before semaglutide initiation were enrolled. The primary endpoint was change in HbA1c from baseline to end of study (EOS; ~ 30weeks, although due to the COVID-19 pandemic, visits up to week 52 were permitted). Secondary endpoints included change in body weight, waist circumference and patient-reported outcomes (PROs). Physicians were to report all episodes of documented or severe hypoglycaemia, fatal events, serious adverse drug reactions, pregnancies and adverse events (AEs) in foetuses/newborn infants; other AEs during the study period could be reported on a voluntary basis. Result: The estimated mean change in HbA1c from baseline to EOS was − 16.3mmol/mol [95% confidence interval (CI): − 18.22, − 14.37] (− 1.5%-points [95% CI − 1.67, − 1.31]; p < 0.0001) among the 171 enrolled patients who completed the study on treatment. Mean body weight change was − 5.8kg (95% CI − 6.75, − 4.94; p < 0.0001). Sensitivity analyses showed similar results. Improvements were also observed in other secondary endpoints, including PROs. No new safety concerns were identified with semaglutide treatment. Conclusion: Patients receiving OW semaglutide experienced statistically significant and clinically relevant reductions from baseline in HbA1c and body weight. These results are in line with those of the SUSTAIN RCTs and support the use of OW semaglutide in routine clinical practice in adults with T2D in the UK. Trial registration: ClinicalTrials.gov Identifier NCT03876015.

Citation

Holmes, P., Bell, H. E., Bozkurt, K., Catarig, A. M., Clark, A., Machell, A., & Sathyapalan, T. (2021). Real-World Use of Once-Weekly Semaglutide in Type 2 Diabetes: Results from the SURE UK Multicentre, Prospective, Observational Study. Diabetes Therapy, https://doi.org/10.1007/s13300-021-01141-8

Journal Article Type Article
Acceptance Date Aug 9, 2021
Online Publication Date Sep 25, 2021
Publication Date Sep 21, 2021
Deposit Date Sep 27, 2021
Publicly Available Date Sep 29, 2021
Journal Diabetes Therapy
Print ISSN 1869-6953
Electronic ISSN 1869-6961
Publisher Springer
Peer Reviewed Peer Reviewed
DOI https://doi.org/10.1007/s13300-021-01141-8
Keywords Type 2 diabetes; Glucagon-like peptide-1 receptor agonist; Semaglutide; Real-world evidence
Public URL https://hull-repository.worktribe.com/output/3844369

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Copyright Statement
© The Author(s) 2021.
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.





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