Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators

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Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators. / Dungan, Kathleen M.; Bardtrum, Lars; Christiansen, Erik; Eliasson, Johanna; Mellbin, Linda; Woo, Vincent C.; Vilsbøll, Tina.

I: Diabetes Therapy, Bind 14, Nr. 8, 2023, s. 1415-1425.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Dungan, KM, Bardtrum, L, Christiansen, E, Eliasson, J, Mellbin, L, Woo, VC & Vilsbøll, T 2023, 'Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators', Diabetes Therapy, bind 14, nr. 8, s. 1415-1425. https://doi.org/10.1007/s13300-023-01413-5

APA

Dungan, K. M., Bardtrum, L., Christiansen, E., Eliasson, J., Mellbin, L., Woo, V. C., & Vilsbøll, T. (2023). Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators. Diabetes Therapy, 14(8), 1415-1425. https://doi.org/10.1007/s13300-023-01413-5

Vancouver

Dungan KM, Bardtrum L, Christiansen E, Eliasson J, Mellbin L, Woo VC o.a. Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators. Diabetes Therapy. 2023;14(8):1415-1425. https://doi.org/10.1007/s13300-023-01413-5

Author

Dungan, Kathleen M. ; Bardtrum, Lars ; Christiansen, Erik ; Eliasson, Johanna ; Mellbin, Linda ; Woo, Vincent C. ; Vilsbøll, Tina. / Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators. I: Diabetes Therapy. 2023 ; Bind 14, Nr. 8. s. 1415-1425.

Bibtex

@article{e63acded31b8471d9e77b2fa62137b5a,
title = "Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators",
abstract = "Introduction: A post hoc analysis of the PIONEER 1–5 and 8 trials assessed the clinically relevant composite endpoints of HbA1c (glycated haemoglobin) reduction ≥ 1% and body weight loss of ≥ 5% or ≥ 10% with orally administered semaglutide versus comparators. Methods: In the PIONEER trials, people with type 2 diabetes were randomised to orally administered semaglutide versus placebo (PIONEER 1, 4, 5 and 8), empagliflozin (PIONEER 2), sitagliptin (PIONEER 3) and liraglutide (PIONEER 4) for 26–78 weeks. This analysis assessed the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% at week 26 and at end of treatment, and the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment. Results: Overall, 3506 people in PIONEER 1–5 and 8 were included. At week 26 and at end of treatment, odds of achieving the composite endpoint of an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% were significantly greater with orally administered semaglutide 14 mg than with placebo (PIONEER 1, 4, 5 and 8; all p < 0.0001), empagliflozin 25 mg (PIONEER 2, p < 0.0001), sitagliptin 100 mg (PIONEER 3, p < 0.0001) and liraglutide 1.8 mg (PIONEER 4, p < 0.0001). Odds of achieving the composite endpoint of HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment were also significantly greater with orally administered semaglutide versus comparators. Conclusion: In PIONEER 1–5 and 8, odds of achieving clinically relevant reductions in both HbA1c and body weight were significantly greater with orally administered semaglutide versus comparators. Graphical Abstract: [Figure not available: see fulltext.]",
keywords = "Body weight loss, Composite endpoint, Glucagon-like peptide 1 analogue, Glycaemic control, Type 2 diabetes",
author = "Dungan, {Kathleen M.} and Lars Bardtrum and Erik Christiansen and Johanna Eliasson and Linda Mellbin and Woo, {Vincent C.} and Tina Vilsb{\o}ll",
note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",
year = "2023",
doi = "10.1007/s13300-023-01413-5",
language = "English",
volume = "14",
pages = "1415--1425",
journal = "Diabetes Therapy",
issn = "1869-6953",
publisher = "Springer",
number = "8",

}

RIS

TY - JOUR

T1 - Greater Combined Reductions of HbA1c ≥ 1.0% and Body Weight Loss ≥ 5.0% or ≥ 10.0% with Orally Administered Semaglutide Versus Comparators

AU - Dungan, Kathleen M.

AU - Bardtrum, Lars

AU - Christiansen, Erik

AU - Eliasson, Johanna

AU - Mellbin, Linda

AU - Woo, Vincent C.

AU - Vilsbøll, Tina

N1 - Publisher Copyright: © 2023, The Author(s).

PY - 2023

Y1 - 2023

N2 - Introduction: A post hoc analysis of the PIONEER 1–5 and 8 trials assessed the clinically relevant composite endpoints of HbA1c (glycated haemoglobin) reduction ≥ 1% and body weight loss of ≥ 5% or ≥ 10% with orally administered semaglutide versus comparators. Methods: In the PIONEER trials, people with type 2 diabetes were randomised to orally administered semaglutide versus placebo (PIONEER 1, 4, 5 and 8), empagliflozin (PIONEER 2), sitagliptin (PIONEER 3) and liraglutide (PIONEER 4) for 26–78 weeks. This analysis assessed the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% at week 26 and at end of treatment, and the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment. Results: Overall, 3506 people in PIONEER 1–5 and 8 were included. At week 26 and at end of treatment, odds of achieving the composite endpoint of an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% were significantly greater with orally administered semaglutide 14 mg than with placebo (PIONEER 1, 4, 5 and 8; all p < 0.0001), empagliflozin 25 mg (PIONEER 2, p < 0.0001), sitagliptin 100 mg (PIONEER 3, p < 0.0001) and liraglutide 1.8 mg (PIONEER 4, p < 0.0001). Odds of achieving the composite endpoint of HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment were also significantly greater with orally administered semaglutide versus comparators. Conclusion: In PIONEER 1–5 and 8, odds of achieving clinically relevant reductions in both HbA1c and body weight were significantly greater with orally administered semaglutide versus comparators. Graphical Abstract: [Figure not available: see fulltext.]

AB - Introduction: A post hoc analysis of the PIONEER 1–5 and 8 trials assessed the clinically relevant composite endpoints of HbA1c (glycated haemoglobin) reduction ≥ 1% and body weight loss of ≥ 5% or ≥ 10% with orally administered semaglutide versus comparators. Methods: In the PIONEER trials, people with type 2 diabetes were randomised to orally administered semaglutide versus placebo (PIONEER 1, 4, 5 and 8), empagliflozin (PIONEER 2), sitagliptin (PIONEER 3) and liraglutide (PIONEER 4) for 26–78 weeks. This analysis assessed the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% at week 26 and at end of treatment, and the proportion of people achieving an HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment. Results: Overall, 3506 people in PIONEER 1–5 and 8 were included. At week 26 and at end of treatment, odds of achieving the composite endpoint of an HbA1c reduction of ≥ 1% and body weight loss of ≥ 5% were significantly greater with orally administered semaglutide 14 mg than with placebo (PIONEER 1, 4, 5 and 8; all p < 0.0001), empagliflozin 25 mg (PIONEER 2, p < 0.0001), sitagliptin 100 mg (PIONEER 3, p < 0.0001) and liraglutide 1.8 mg (PIONEER 4, p < 0.0001). Odds of achieving the composite endpoint of HbA1c reduction of ≥ 1% and body weight loss of ≥ 10% at end of treatment were also significantly greater with orally administered semaglutide versus comparators. Conclusion: In PIONEER 1–5 and 8, odds of achieving clinically relevant reductions in both HbA1c and body weight were significantly greater with orally administered semaglutide versus comparators. Graphical Abstract: [Figure not available: see fulltext.]

KW - Body weight loss

KW - Composite endpoint

KW - Glucagon-like peptide 1 analogue

KW - Glycaemic control

KW - Type 2 diabetes

U2 - 10.1007/s13300-023-01413-5

DO - 10.1007/s13300-023-01413-5

M3 - Journal article

C2 - 37256503

AN - SCOPUS:85160710888

VL - 14

SP - 1415

EP - 1425

JO - Diabetes Therapy

JF - Diabetes Therapy

SN - 1869-6953

IS - 8

ER -

ID: 365702143