Diabetologie und Stoffwechsel 2021; 16(S 01): S7
DOI: 10.1055/s-0041-1727310
01. Klinische Diabetologie

Oral Semaglutide vs. Sitagliptin: Efficacy by Baseline HbA1c and Background OAD in PIONEER 3

M Hauser
1   Novo Nordisk Pharma GmbH, Medical Affairs, Mainz, Germany
,
J Rosenstock
2   Medical City Dallas, Dallas Diabetes Research Center, Dallas, United States
,
D Allison
3   Hillcrest Family Health Center, Hillcrest Family Health Center, Waco, Texas, United States
,
AL Birkenfeld
4   Universitätsklinikum Tübingen Med. Klinik, Innere Medizin IV, Tübingen, Germany
,
TM Blicher
5   Novo Nordisk A / S, Medical Affairs, Søborg, Denmark
,
S Deenadayalan
5   Novo Nordisk A / S, Medical Affairs, Søborg, Denmark
,
A Kousholt
6   Novo Nordisk A / S, Biostatistics, Søborg, Denmark
,
M Davies
7   University of Leicester, Diabetes Research Centre, Leicester, United Kingdom
› Author Affiliations
 
 

    Exploratory analyses of PIONEER 3 (NCT02607865) assessed the efficacy (HbA1c change from baseline [BL], achievement of HbA < 7.0 %) of oral semaglutide (sema; 3, 7, or 14 mg), a novel oral GLP-1 receptor agonist, vs. sitagliptin (sita) 100 mg at week 26 by BL HbA1c and background OAD in pts with T2 D uncontrolled on metformin ± sulfonylurea. HbA was reduced across all BL HbA1a and OAD groups in all treatment arms; reductions were greater with higher BL HbA1c. HbA1c reductions were significantly greater with oral sema 7 and 14 mg vs. sita in all groups, except for 7 mg in the HbA1c ≤ 8.0 % group (Figure 1). Achievement of HbA1c < 7.0 % was greater with oral sema 7 and 14 mg vs. sita in all groups (Figure 2). In conclusion, oral sema 7 and 14 mg significantly improved glycaemic control vs. sita across most HbA1c groups, and irrespective of background OAD use.


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    Interessenskonflikt

    Funding Novo Nordisk A / S

    Disclosure J. Rosenstock: Research Support; Self; AstraZeneca, Bristol-Myers Squibb Company, Genentech,

    Inc., GlaxoSmithKline plc., Lexicon Pharmaceuticals, Inc., Melior Pharmaceuticals, Inc., Bukwang Pharm. Co.,

    Ltd., Merck & Co., Inc., Oramed Pharmaceuticals, PegBio Co., Ltd., Pzer Inc. Other Relationship; Self;

    Boehringer Ingelheim International GmbH, Eli Lilly and Company, Intarcia Therapeutics, Inc., Janssen

    Pharmaceuticals, Inc., Novo Nordisk Inc., Sano. D.C. Allison: Advisory Panel; Self; Novo Nordisk Inc. Research

    Support; Self; Bayer US, Boehringer Ingelheim Pharmaceuticals, Inc., Janssen Pharmaceuticals, Inc., Kowa

    Pharmaceutical Europe Co. Ltd., Sano. A.L. Birkenfeld: None. T.M. Blicher: Employee; Self; Novo Nordisk A / S.

    S. Deenadayalan: Employee; Self; Novo Nordisk A / S. Stock / Shareholder; Self; Novo Nordisk A / S. A. Kousholt:

    Employee; Self; Novo Nordisk A / S. M.J. Davies: Advisory Panel; Self; Eli Lilly and Company, Janssen Global

    Services, LLC., Novo Nordisk A / S, Sano-Aventis, Servier. Research Support; Self; Boehringer Ingelheim

    International GmbH, Novo Nordisk Foundation. Speaker’s Bureau; Self; Boehringer Ingelheim International

    GmbH, Eli Lilly and Company, Novo Nordisk A / S, Sano-Aventis, Takeda Pharmaceutical Company Limited.

    Publication History

    Article published online:
    06 May 2021

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