Aims: The current study was designed to evaluate the effect of switching from subcutaneous dulaglutide 0.75 mg weekly to oral semaglutide 7 mg daily on glycemic control, as reflected by hemoglobin A1c (HbA1c), occasional plasma glucose (PG) and glycoalbumin (GA) in real-world clinical practice in our hospital.
Patients and Methods: A search of electronic medical records from January to September 2023 was performed for patients who had received dulaglutide for type 2 diabetes and were switched to oral semaglutide because of a chronic shortage of the supply of dulaglutide. A total of 19 patients were enrolled and data for these patients were evaluated until the end of March 2024.
Results: All patients continued to take oral semaglutide during the observational period after the switch. After the change to oral semaglutide, there were no significant differences in HbA1c, PG and GA among time points of the final visit before baseline, at baseline (the time of the switch), and after 3 and 6 months. Low-density lipoprotein cholesterol (LDL-C), estimated glomerular filtration rate (eGFR), and body weight (BW) also did not differ significantly among all of these time points.
Conclusion: A switch from subcutaneous dulaglutide 0.75 mg weekly to oral semaglutide 7 mg daily did not influence glycemic control, as reflected by HbA1c, PG and GA levels, or LDL-C, eGFR, and BW over a 6-month observational period. The tolerability to this change was basically satisfactory.
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