Glycaemic control, body weight, and safety of tirzepatide versus dulaglutide by baseline glycated haemoglobin level in Japanese patients with type 2 diabetes: A subgroup analysis of the SURPASS J-mono study

被引:0
作者
Osonoi, Takeshi [1 ]
Oura, Tomonori [2 ]
Hirase, Tetsuaki [2 ]
机构
[1] Nakakinen Clin, Ibaraki, Japan
[2] Eli Lilly Japan KK, Japan Drug Dev & Med Affairs, 5-1-28 Isogami Dori,Chuo Ku, Kobe, Hyogo 6510086, Japan
关键词
body weight; dulaglutide; glycaemic control; Japan; tirzepatide; type; 2; diabetes; PEPTIDE-1 RECEPTOR AGONISTS; DUAL GIP; MELLITUS; RISK;
D O I
10.1111/dom.15296
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: To evaluate glycaemic control, body weight, and safety outcomes following treatment with tirzepatide or dulaglutide in patients with type 2 diabetes (T2D) with a baseline haemoglobin (HbA1c) level of <= 8.5% (<= 69 mmol/mol) versus >8.5% (>69 mmol/mol). Materials and methods:<bold> </bold>SURPASS J-mono was a 52-week, multicentre, randomized, double-blind, parallel, active-controlled, phase 3 study conducted in Japan. In this exploratory subgroup analysis of SURPASS J-mono, we examined mean change in HbA1c and body weight and the incidence of adverse events (AEs) in patients with a baseline HbA1c of <= 8.5% versus >8.5% after treatment with tirzepatide (5, 10 or 15 mg) or dulaglutide 0.75 mg. Results:<bold> </bold>Of 636 randomized participants, 203 had a baseline HbA1c of >8.5% and 433 had a baseline HbA1c of <= 8.5% (range >= 7.0% to <= 10.0%). Both subgroups showed significantly greater reductions in HbA1c and body weight with any-dose tirzepatide versus dulaglutide 0.75 mg, with greater HbA1c reductions observed in patients with a baseline HbA1c of >8.5% treated with tirzepatide (least squares mean [LSM] differences of -3.13% to -3.86%) or dulaglutide (LSM -1.81%) compared with patients with a baseline HbA1c of <= 8.5% (LSM -2.00% to -2.32%) or dulaglutide (LSM -1.05%; treatment-by-baseline HbA1c subgroup interaction P <= 0.001). For the tirzepatide treatment arms, LSM change from baseline in body weight ranged from -6.7 to -10.7 kg for the baseline HbA1c <= 8.5% subgroup and from -4.0 to -10.6 kg for the baseline HbA1c >8.5% subgroup, compared with -0.6 kg and -0.4 kg, respectively, for the dulaglutide arm. The incidence of hypoglycaemia was low, with no substantial difference in hypoglycaemia or treatment-emergent AEs between subgroups. Conclusions:<bold> </bold>Regardless of baseline HbA1c (<= 8.5% or >8.5%), tirzepatide at doses of 5, 10 and 15 mg is effective in Japanese patients with T2D compared with dulaglutide 0.75 mg in terms of glycaemic control and body weight reduction, with an adequate safety profile consistent with previous reports.
引用
收藏
页码:126 / 134
页数:9
相关论文
共 28 条
  • [1] Impact of weight reduction on insulin resistance, adhesive molecules and adipokines dysregulation among obese type 2 diabetic patients
    Abd El-Kader, Shehab M.
    Al-Jiffri, Osama H.
    [J]. AFRICAN HEALTH SCIENCES, 2018, 18 (04) : 873 - 883
  • [2] American Diabetes Association, 2022, Clin Diabetes, V40, P10, DOI 10.2337/cd22-as01
  • [3] Araki E, 2020, DIABETOL INT, V11, P165, DOI [10.1007/s13340-020-00439-5, 10.1111/jdi.13306]
  • [4] Efficacy of once-weekly tirzepatide versus once-daily insulin degludec on glycaemic control measured by continuous glucose monitoring in adults with type 2 diabetes (SURPASS-3 CGM): a substudy of the randomised, open-label, parallel-group, phase 3 SURPASS-3 trial
    Battelino, Tadej
    Bergenstal, Richard M.
    Rodriguez, Angel
    Fernandez Lando, Laura
    Bray, Ross
    Tong, Zhentao
    Brown, Katelyn
    [J]. LANCET DIABETES & ENDOCRINOLOGY, 2022, 10 (06) : 407 - 417
  • [5] LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: From discovery to clinical proof of concept
    Coskun, Tamer
    Sloop, Kyle W.
    Loghin, Corina
    Alsina-Fernandez, Jorge
    Urva, Shweta
    Bokvist, Krister B.
    Cui, Xuewei
    Briere, Daniel A.
    Cabrera, Over
    Roell, William C.
    Kuchibhotla, Uma
    Moyers, Julie S.
    Benson, Charles T.
    Gimeno, Ruth E.
    D'Alessio, David A.
    Haupt, Axel
    [J]. MOLECULAR METABOLISM, 2018, 18 : 3 - 14
  • [6] Effect of Subcutaneous Tirzepatide vs Placebo Added to Titrated Insulin Glargine on Glycemic Control in Patients With Type 2 Diabetes The SURPASS-5 Randomized Clinical Trial
    Dahl, Dominik
    Onishi, Yukiko
    Norwood, Paul
    Huh, Ruth
    Bray, Ross
    Patel, Hiren
    Rodriguez, Angel
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2022, 327 (06): : 534 - 545
  • [7] Tirzepatide versus insulin glargine in type 2 diabetes and increased cardiovascular risk (SURPASS-4): a randomised, open-label, parallel-group, multicentre, phase 3 trial
    Del Prato, Stefano
    Kahn, Steven E.
    Pavo, Imre
    Weerakkody, Govinda J.
    Yang, Zhengyu
    Doupis, John
    Aizenberg, Diego
    Wynne, Alan G.
    Riesmeyer, Jeffrey S.
    Heine, Robert J.
    Wiese, Russell J.
    [J]. LANCET, 2021, 398 (10313) : 1811 - 1824
  • [8] European Medicines Agency, MOUNJ
  • [9] Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes
    Frias, Juan P.
    Davies, Melanie J.
    Rosenstock, Julio
    Manghi, Federico C. Perez
    Lando, Laura Fernandez
    Bergman, Brandon K.
    Liu, Bing
    Cui, Xuewei
    Brown, Katelyn
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (06) : 503 - 515
  • [10] Effects of subcutaneous tirzepatide versus placebo or semaglutide on pancreatic islet function and insulin sensitivity in adults with type 2 diabetes: a multicentre, randomised, double-blind, parallel-arm, phase 1 clinical trial
    Heise, Tim
    Mari, Andrea
    DeVries, J. Hans
    Urva, Shweta
    Li, Jing
    Pratt, Edward John
    Coskun, Tamer
    Thomas, Melissa K.
    Mather, Kieren J.
    Haupt, Axel
    Milicevic, Zvonko
    [J]. LANCET DIABETES & ENDOCRINOLOGY, 2022, 10 (06) : 418 - 429