Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators: An exploratory analysis of the PIONEER studies

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Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators : An exploratory analysis of the PIONEER studies. / Rosenstock, Julio; Cariou, Bertrand; Eliasson, Johanna; Frappin, Guillaume; Kaltoft, Margit S.; Montanya, Eduard; Knop, Filip K.

In: Diabetes, Obesity and Metabolism, Vol. 26, No. 2, 2024, p. 532-539.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rosenstock, J, Cariou, B, Eliasson, J, Frappin, G, Kaltoft, MS, Montanya, E & Knop, FK 2024, 'Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators: An exploratory analysis of the PIONEER studies', Diabetes, Obesity and Metabolism, vol. 26, no. 2, pp. 532-539. https://doi.org/10.1111/dom.15339

APA

Rosenstock, J., Cariou, B., Eliasson, J., Frappin, G., Kaltoft, M. S., Montanya, E., & Knop, F. K. (2024). Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators: An exploratory analysis of the PIONEER studies. Diabetes, Obesity and Metabolism, 26(2), 532-539. https://doi.org/10.1111/dom.15339

Vancouver

Rosenstock J, Cariou B, Eliasson J, Frappin G, Kaltoft MS, Montanya E et al. Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators: An exploratory analysis of the PIONEER studies. Diabetes, Obesity and Metabolism. 2024;26(2):532-539. https://doi.org/10.1111/dom.15339

Author

Rosenstock, Julio ; Cariou, Bertrand ; Eliasson, Johanna ; Frappin, Guillaume ; Kaltoft, Margit S. ; Montanya, Eduard ; Knop, Filip K. / Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators : An exploratory analysis of the PIONEER studies. In: Diabetes, Obesity and Metabolism. 2024 ; Vol. 26, No. 2. pp. 532-539.

Bibtex

@article{56dd2288fd1d42acb2c6cb1b0abf1bbc,
title = "Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators: An exploratory analysis of the PIONEER studies",
abstract = "Aim: To assess how long participants with type 2 diabetes spent with HbA1c less than 7.0% and how likely they were to maintain this target with oral semaglutide 7 mg versus sitagliptin 100 mg or oral semaglutide 14 mg versus empagliflozin 25 mg, sitagliptin 100 mg or subcutaneous liraglutide 1.8 mg. Materials and Methods: Analyses used on-treatment data without rescue medication for all randomized participants (semaglutide [approved maintenance doses], n = 1880; comparators [not including placebo], n = 1412). Duration of time with HbA1c less than 7.0% was calculated using an HbA1c time curve. A binary endpoint of achieving HbA1c less than 7.0% at weeks 26 (week 24 for PIONEER 7) and 52 of each trial (and week 78 for PIONEER 3) was analysed. Results: Mean duration of time with HbA1c less than 7.0% was greater with oral semaglutide 7 mg versus sitagliptin in PIONEER 3 (27 vs. 22 weeks) and with oral semaglutide 14 mg versus empagliflozin and sitagliptin (27-34 vs. 19 vs. 22 weeks, respectively), and similar versus subcutaneous liraglutide. A greater proportion of participants achieved and maintained HbA1c less than 7.0% for more than 75% of the trial with oral semaglutide 14 mg versus oral comparators. The odds of achieving HbA1c less than 7.0% at weeks 24/26 and 52/78 were significantly greater with oral semaglutide 14 mg versus oral comparators or subcutaneous liraglutide, and with oral semaglutide 7 mg versus sitagliptin. Conclusions: Oral semaglutide 7 and 14 mg resulted in greater time spent with HbA1c less than 7.0%, and a greater likelihood of achieving and maintaining HbA1c less than 7.0% versus oral comparators.",
keywords = "antidiabetic drug, GLP-1 analogue, glycaemic control, incretin therapy, semaglutide, type 2 diabetes",
author = "Julio Rosenstock and Bertrand Cariou and Johanna Eliasson and Guillaume Frappin and Kaltoft, {Margit S.} and Eduard Montanya and Knop, {Filip K.}",
note = "Publisher Copyright: {\textcopyright} 2023 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.",
year = "2024",
doi = "10.1111/dom.15339",
language = "English",
volume = "26",
pages = "532--539",
journal = "Diabetes, Obesity and Metabolism",
issn = "1462-8902",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Greater time spent with HbA1c less than 7.0% with oral semaglutide versus oral comparators

T2 - An exploratory analysis of the PIONEER studies

AU - Rosenstock, Julio

AU - Cariou, Bertrand

AU - Eliasson, Johanna

AU - Frappin, Guillaume

AU - Kaltoft, Margit S.

AU - Montanya, Eduard

AU - Knop, Filip K.

N1 - Publisher Copyright: © 2023 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

PY - 2024

Y1 - 2024

N2 - Aim: To assess how long participants with type 2 diabetes spent with HbA1c less than 7.0% and how likely they were to maintain this target with oral semaglutide 7 mg versus sitagliptin 100 mg or oral semaglutide 14 mg versus empagliflozin 25 mg, sitagliptin 100 mg or subcutaneous liraglutide 1.8 mg. Materials and Methods: Analyses used on-treatment data without rescue medication for all randomized participants (semaglutide [approved maintenance doses], n = 1880; comparators [not including placebo], n = 1412). Duration of time with HbA1c less than 7.0% was calculated using an HbA1c time curve. A binary endpoint of achieving HbA1c less than 7.0% at weeks 26 (week 24 for PIONEER 7) and 52 of each trial (and week 78 for PIONEER 3) was analysed. Results: Mean duration of time with HbA1c less than 7.0% was greater with oral semaglutide 7 mg versus sitagliptin in PIONEER 3 (27 vs. 22 weeks) and with oral semaglutide 14 mg versus empagliflozin and sitagliptin (27-34 vs. 19 vs. 22 weeks, respectively), and similar versus subcutaneous liraglutide. A greater proportion of participants achieved and maintained HbA1c less than 7.0% for more than 75% of the trial with oral semaglutide 14 mg versus oral comparators. The odds of achieving HbA1c less than 7.0% at weeks 24/26 and 52/78 were significantly greater with oral semaglutide 14 mg versus oral comparators or subcutaneous liraglutide, and with oral semaglutide 7 mg versus sitagliptin. Conclusions: Oral semaglutide 7 and 14 mg resulted in greater time spent with HbA1c less than 7.0%, and a greater likelihood of achieving and maintaining HbA1c less than 7.0% versus oral comparators.

AB - Aim: To assess how long participants with type 2 diabetes spent with HbA1c less than 7.0% and how likely they were to maintain this target with oral semaglutide 7 mg versus sitagliptin 100 mg or oral semaglutide 14 mg versus empagliflozin 25 mg, sitagliptin 100 mg or subcutaneous liraglutide 1.8 mg. Materials and Methods: Analyses used on-treatment data without rescue medication for all randomized participants (semaglutide [approved maintenance doses], n = 1880; comparators [not including placebo], n = 1412). Duration of time with HbA1c less than 7.0% was calculated using an HbA1c time curve. A binary endpoint of achieving HbA1c less than 7.0% at weeks 26 (week 24 for PIONEER 7) and 52 of each trial (and week 78 for PIONEER 3) was analysed. Results: Mean duration of time with HbA1c less than 7.0% was greater with oral semaglutide 7 mg versus sitagliptin in PIONEER 3 (27 vs. 22 weeks) and with oral semaglutide 14 mg versus empagliflozin and sitagliptin (27-34 vs. 19 vs. 22 weeks, respectively), and similar versus subcutaneous liraglutide. A greater proportion of participants achieved and maintained HbA1c less than 7.0% for more than 75% of the trial with oral semaglutide 14 mg versus oral comparators. The odds of achieving HbA1c less than 7.0% at weeks 24/26 and 52/78 were significantly greater with oral semaglutide 14 mg versus oral comparators or subcutaneous liraglutide, and with oral semaglutide 7 mg versus sitagliptin. Conclusions: Oral semaglutide 7 and 14 mg resulted in greater time spent with HbA1c less than 7.0%, and a greater likelihood of achieving and maintaining HbA1c less than 7.0% versus oral comparators.

KW - antidiabetic drug

KW - GLP-1 analogue

KW - glycaemic control

KW - incretin therapy

KW - semaglutide

KW - type 2 diabetes

U2 - 10.1111/dom.15339

DO - 10.1111/dom.15339

M3 - Journal article

C2 - 37935463

AN - SCOPUS:85176273837

VL - 26

SP - 532

EP - 539

JO - Diabetes, Obesity and Metabolism

JF - Diabetes, Obesity and Metabolism

SN - 1462-8902

IS - 2

ER -

ID: 379652886