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Emerging Treatments and Technologies

An Open, Randomized, Parallel-Group Study to Compare the Efficacy and Safety Profile of Inhaled Human Insulin (Exubera) With Glibenclamide as Adjunctive Therapy in Patients With Type 2 Diabetes Poorly Controlled on Metformin

  1. Anthony H. Barnett, BSC, MD, FRCP1,
  2. Manfred Dreyer, MD2,
  3. Peter Lange, MD3,
  4. Marjana Serdarevic-Pehar, MD4 and
  5. on behalf of the Exubera Phase III Study Group
  1. 1University of Birmingham and Heart of England National Health Service Foundation Trust (Teaching), Birmingham, U.K.
  2. 2Department of Diabetes and Metabolism, Bethanien Krankenhaus, Hamburg, Germany
  3. 3Department of Respiratory Medicine, Hvidovre University Hospital, Hvidovre, Denmark
  4. 4Pfizer, Sandwich, U.K.
  1. Address correspondence and reprint requests to A.H. Barnett, Undergraduate Centre, Birmingham Heartlands Hospital, Bordesley Green East, Birmingham, B9 5SS, U.K. E-mail: anthony.barnett{at}heartofengland.nhs.uk
Diabetes Care 2006 Aug; 29(8): 1818-1825. https://doi.org/10.2337/dc05-1880
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Abstract

OBJECTIVE—To compare the efficacy and safety profile of adding inhaled human insulin (INH) (Exubera) or glibenclamide to metformin monotherapy in patients with poorly controlled type 2 diabetes.

RESEARCH DESIGN AND METHODS—We conducted an open-label, parallel, 24-week multicenter trial. Patients uncontrolled on metformin were randomized to adjunctive INH (n = 243) or glibenclamide (n = 233). Before randomization, patients were divided into two HbA1c (A1C) arms: ≥8 to ≤9.5% (moderately high) and >9.5 to ≤12% (very high). The primary efficacy end point was A1C change from baseline.

RESULTS—Mean adjusted A1C changes from baseline were −2.03 and −1.88% in the INH and glibenclamide groups, respectively; between-treatment difference −0.17% (95% CI −0.34 to 0.01; P = 0.058), consistent with the noninferiority criterion. In the A1C >9.5% arm, inhaled insulin demonstrated a significantly greater reduction in A1C than glibenclamide, between-treatment difference −0.37% (−0.62 to −0.12; P = 0.004). In the A1C ≤9.5% arm, between-treatment difference was 0.04% (−0.19 to 0.27; P = 0.733). Hypoglycemia (events per subject-month) was greater with INH (0.18) than glibenclamide (0.08), risk ratio 2.24 (1.58–3.16), but there were no associated discontinuations. Other adverse events, except increased cough in the INH group, were similar. At week 24, changes from baseline in pulmonary function parameters were small. Insulin antibody binding increased more with INH but did not have any associated clinical manifestations.

CONCLUSIONS—In patients with type 2 diabetes poorly controlled on metformin, adding INH or glibenclamide was similarly effective in improving glycemic control, and both were well tolerated. A predefined subgroup with very high A1C (>9.5%) was more effectively treated with the addition of INH.

  • ADA, American Diabetes Association
  • DLco, carbon monoxide transfer factor
  • FEV1, forced expiratory volume in 1 s
  • INH, inhaled human insulin

Footnotes

  • A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted May 18, 2006.
    • Received October 4, 2005.
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An Open, Randomized, Parallel-Group Study to Compare the Efficacy and Safety Profile of Inhaled Human Insulin (Exubera) With Glibenclamide as Adjunctive Therapy in Patients With Type 2 Diabetes Poorly Controlled on Metformin
Anthony H. Barnett, Manfred Dreyer, Peter Lange, Marjana Serdarevic-Pehar
Diabetes Care Aug 2006, 29 (8) 1818-1825; DOI: 10.2337/dc05-1880

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An Open, Randomized, Parallel-Group Study to Compare the Efficacy and Safety Profile of Inhaled Human Insulin (Exubera) With Glibenclamide as Adjunctive Therapy in Patients With Type 2 Diabetes Poorly Controlled on Metformin
Anthony H. Barnett, Manfred Dreyer, Peter Lange, Marjana Serdarevic-Pehar
Diabetes Care Aug 2006, 29 (8) 1818-1825; DOI: 10.2337/dc05-1880
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