INTRODUCTION: The PIONEER REAL India study assessed the effectiveness of oral semaglutide in adults with type 2 diabetes (T2D).
METHODS: This was a 34-44-week, multicenter, non-interventional study in participants who had not previously received injectable glucose-lowering medications and had initiated treatment with oral semaglutide. Change in HbAfrom baseline to end-of-study (EoS) was the primary endpoint. Change in body weight, proportion of participants achieving HbA<7% and HbAreduction ≥1%-points plus body weight reduction ≥3% or ≥5%, also changes in HbAby baseline HbA(≤9% and >9%) from baseline to EoS were assessed. Here, we present the results from on-treatment analyses.
RESULTS: Of 388 enrolled, 70.1% of participants completed the study. At baseline, the mean age and T2D duration of the study population were 50.1 and 6.3 years; mean HbAand body weight were 9.0% and 89.0 kg, respectively. Estimated mean changes (95% confidence interval, CI) in HbAand body weight were - 1.78%-points (-1.88, -1.68;< 0.0001) and - 7.23 kg (-7.84, -6.63;< 0.0001), respectively. At EoS, 34.2% achieved HbA<7%. Estimated mean HbAchanges (95% CI) for participants with baseline HbA≤9% and >9% were - 0.93%-points (-1.07, -0.79;< 0.0001) and - 2.48%-points (-2.60, -2.35;< 0.0001), respectively. No new safety signals were observed.
CONCLUSIONS: Individuals with T2D treated with once-daily oral semaglutide experienced significant reductions in HbAand body weight, without any new safety events. These findings will add to the decision-making for initiating oral semaglutide in individuals with T2D in India.NCT05502562.
Authors
Sanyal, Debmalya; Saboo, Banshi; Phatak, Sanjeev R; Kumar, Prasanna K M; Basu, Debasis; Verma, Nikhil; Nair, Arjun; Bhattacharjee, Kingshuk; Aneja, Pankaj; Makkar, Brij M M; Negalur, Vijay; Mithal, Ambrish; Unnikrishnan, Ambika G
Keywords
Body weightglucagon-like peptide-1 receptor agonistglycemic controloral semaglutidereal-world studytype 2 diabetes