Literature DB >> 19706990

Safety, tolerability, pharmacokinetics, and pharmacodynamics of exenatide once weekly in Japanese patients with type 2 diabetes.

Kazuya Iwamoto1, Risa Nasu, Ayuko Yamamura, Prajakti A Kothare, Kenneth Mace, Anne M Wolka, Helle Linnebjerg.   

Abstract

This randomized, placebo-controlled, double-blind, parallel study assessed the safety, tolerability, pharmacokinetics, and pharmacodynamics of exenatide once weekly (QW) in 30 Japanese patients with type 2 diabetes (T2D) suboptimally controlled by diet and exercise alone or combined with biguanide, sulfonylurea, thiazolidinedione, or combinations of these agents (58.6% male; 58+/-9 years; body mass index 26.3+/-2.9 kg/m(2); hemoglobin A(1c) [HbA(1c)] 7.4+/-0.8%; fasting plasma glucose [FPG] 156.1+/-29.1 mg/dL; duration of T2D 6+/-5 years; means +/- SD). Patients were randomized in a 1:1:1 ratio to subcutaneous placebo QW, exenatide QW 0.8 mg, or exenatide QW 2.0 mg for 10 weeks. All evaluable patients were analyzed (placebo QW, n=10; exenatide QW 0.8 mg, n=10; exenatide QW 2.0 mg, n=9), unless otherwise stated. Steady-state plasma exenatide concentrations were observed by Week 8 of the study. For the evaluable pharmacokinetic population, geometric mean (90% confidence interval) steady-state plasma concentrations (pg/mL) were 81.2 (68.3-96.4) and 344.5 (256.5-462.7) with exenatide QW 0.8 mg (n=8) and exenatide QW 2.0 mg (n=5), respectively. Baseline-to-Week 10 glycemic improvements with placebo QW, exenatide QW 0.8 mg, and exenatide QW 2.0 mg, respectively, were: HbA(1c) (%): -0.4+/-0.3, -1.0+/-0.7, and -1.5+/-0.7; FPG (mg/dL): -20.5+/-20.4, -25.2+/-10.9, and -50.8+/-27.8; and 2-hour postprandial plasma glucose excursions (mg/dL): -8.8+/-26.9, -50.0+/-41.1, and -59.7+/-26.8 (means +/- SD). No serious adverse events (AEs) were reported and no AEs led to study discontinuation in any group. The most frequent AE observed was mild-to-moderate injection site induration. No serious hypoglycemia was reported. Exenatide QW for 10 weeks was well tolerated and improved short-term glycemic control in Japanese patients with suboptimally controlled T2D.

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Year:  2009        PMID: 19706990     DOI: 10.1507/endocrj.k09e-147

Source DB:  PubMed          Journal:  Endocr J        ISSN: 0918-8959            Impact factor:   2.349


  17 in total

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2.  Hydrogel drug delivery system with predictable and tunable drug release and degradation rates.

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Authors:  Mikkel Christensen; Filip K Knop
Journal:  Curr Diab Rep       Date:  2010-04       Impact factor: 4.810

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Authors:  Yahiya Y Syed; Paul L McCormack
Journal:  Drugs       Date:  2015-07       Impact factor: 9.546

Review 5.  Exenatide extended-release: a review of its use in type 2 diabetes mellitus.

Authors:  Lesley J Scott
Journal:  Drugs       Date:  2012-08-20       Impact factor: 9.546

6.  Exenatide once weekly: clinical outcomes and patient satisfaction.

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Journal:  Patient Prefer Adherence       Date:  2010-09-07       Impact factor: 2.711

7.  Incretin mimetics: a novel therapeutic option for patients with type 2 diabetes - a review.

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8.  Efficacy and safety of exenatide once-weekly vs exenatide twice-daily in Asian patients with type 2 diabetes mellitus.

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Review 9.  Efficacy and Acceptability of Glycemic Control of Glucagon-Like Peptide-1 Receptor Agonists among Type 2 Diabetes: A Systematic Review and Network Meta-Analysis.

Authors:  Zhixia Li; Yuan Zhang; Xiaochi Quan; Zhirong Yang; Xiantao Zeng; Linong Ji; Feng Sun; Siyan Zhan
Journal:  PLoS One       Date:  2016-05-09       Impact factor: 3.240

10.  Exenatide extended-release; clinical trials, patient preference, and economic considerations.

Authors:  Sheila A Doggrell
Journal:  Patient Prefer Adherence       Date:  2013-01-09       Impact factor: 2.711

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