Real-world use of once-weekly semaglutide in patients with type 2 diabetes: Results from the SURE Switzerland multicentre, prospective, observational study
Gottfried Rudofsky, Andrei‐Mircea Catarig, Lucie Favre, Katrine Grau, Susan Häfliger, Robert V. Thomann, Bernd Schultes
Abstract
Aims: SURE Switzerland (NCT03631186) investigated real-world once-weekly (OW) semaglutide use in adults with type 2 diabetes (T2D). Methods: This multicentre, prospective, observational study enrolled adults with T2D with ! 1 documented HbA 1c value 12 weeks before semaglutide initiation. Primary endpoint was change in HbA 1c from baseline to end of study (EOS; ~30 weeks). Secondary endpoints included changes in body weight (BW) and waist circumference (WC), and the proportion of patients achieving HbA 1c < 8.0%, <7.5% and <7.0% at EOS. Semaglutide dose at EOS was a prespecified exploratory endpoint. Results: Overall, 214 patients initiated semaglutide (baseline HbA 1c 7.8% [62 mmol/mol], BW 99.9 kg and WC 117.4 cm); 187 attended the EOS visit. At EOS, 175 (81.8%) were still receiving semaglutide (mean [SD] dose 0.78 [0.29] mg); in those patients, mean HbA 1c reduced by 0.8 [95% CI 1.01;0.68] %-points (9 [11;7] mmol/mol), BW by 5.0 kg [5.73;4.24] and WC by 4.8 cm [5.75;3.79] (all p < 0.0001). At EOS, 85.9%, 76.5% and 55.9% patients achieved, respectively, HbA 1c < 8.0%, <7.5% and < 7.0%. No new safety signals were identified. Conclusions: Patients with T2D in Switzerland initiating OW semaglutide experienced clinically relevant glycaemic control and BW improvements in a real-world setting, supporting semaglutide use in routine clinical practice.