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Oral Semaglutide Versus Empagliflozin in Patients With Type 2 Diabetes Uncontrolled on Metformin: The PIONEER 2 Trial.
Rodbard, Helena W; Rosenstock, Julio; Canani, Luis H; Deerochanawong, Chaicharn; Gumprecht, Janusz; Lindberg, Søren Østergaard; Lingvay, Ildiko; Søndergaard, Anette Luther; Treppendahl, Marianne Bach; Montanya, Eduard.
Afiliação
  • Rodbard HW; Endocrine and Metabolic Consultants, Rockville, MD hrodbard@comcast.net.
  • Rosenstock J; Dallas Diabetes Research Center at Medical City, Dallas, TX.
  • Canani LH; Endocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
  • Deerochanawong C; Rajavithi Hospital, Rangsit Medical School, Bangkok, Thailand.
  • Gumprecht J; Medical University of Silesia, Katowice, Poland.
  • Lindberg SØ; Novo Nordisk A/S, Søborg, Denmark.
  • Lingvay I; Departments of Internal Medicine and Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, TX.
  • Søndergaard AL; Novo Nordisk A/S, Søborg, Denmark.
  • Treppendahl MB; Novo Nordisk A/S, Søborg, Denmark.
Diabetes Care ; 42(12): 2272-2281, 2019 12.
Article em En | MEDLINE | ID: mdl-31530666
ABSTRACT

OBJECTIVE:

Efficacy and safety of the glucagon-like peptide 1 (GLP-1) analog oral semaglutide and the sodium-glucose cotransporter 2 inhibitor empagliflozin were compared in patients with type 2 diabetes uncontrolled on metformin. RESEARCH DESIGN AND

METHODS:

Patients were randomized to once-daily open-label treatment with oral semaglutide 14 mg (n = 412) or empagliflozin 25 mg (n = 410) in a 52-week trial. Key end points were change from baseline to week 26 in HbA1c (primary) and body weight (confirmatory secondary). Two estimands addressed efficacy-related questions treatment policy (regardless of trial product discontinuation or rescue medication) and trial product (on trial product without rescue medication) in all randomized patients.

RESULTS:

Four hundred (97.1%) patients in the oral semaglutide group and 387 (94.4%) in the empagliflozin group completed the trial. Oral semaglutide provided superior reductions in HbA1c versus empagliflozin at week 26 (treatment policy -1.3% vs. -0.9% [-14 vs. -9 mmol/mol], estimated treatment difference [ETD] -0.4% [95% CI -0.6, -0.3] [-5 mmol/mol (-6, -3)]; P < 0.0001). The treatment difference in HbA1c significantly favored oral semaglutide at week 26 for the trial product estimand (-1.4% vs. -0.9% [-15 vs. -9 mmol/mol], ETD -0.5% [95% CI -0.7, -0.4] [-6 mmol/mol (-7, -5)]; P < 0.0001) and at week 52 for both estimands (P < 0.0001). Superior weight loss was not confirmed at week 26 (treatment policy), but oral semaglutide was significantly better than empagliflozin at week 52 (trial product -4.7 vs. -3.8 kg; P = 0.0114). Gastrointestinal adverse events were more common with oral semaglutide.

CONCLUSIONS:

Oral semaglutide was superior to empagliflozin in reducing HbA1c but not body weight at 26 weeks in patients with type 2 diabetes uncontrolled on metformin. At week 52, HbA1c and body weight (trial product estimand) were significantly reduced versus empagliflozin. Oral semaglutide was well tolerated within the established safety profile of GLP-1 receptor agonists.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos Benzidrílicos / Diabetes Mellitus Tipo 2 / Peptídeos Semelhantes ao Glucagon / Glucosídeos / Hipoglicemiantes / Metformina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos Benzidrílicos / Diabetes Mellitus Tipo 2 / Peptídeos Semelhantes ao Glucagon / Glucosídeos / Hipoglicemiantes / Metformina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article