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Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects.

Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects. Research Abstract Details 

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  • Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects. Abstract Text:

    je gernJe Gern,ck stoneCk Stone,m nakanoM Nakano,db muchmoreDb Muchmore,a A ,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,ww busseWw Busse,j e gernJ E Gern,c k stoneC K Stone,m nakanoM Nakano,d b muchmoreD B Muchmore,a de la peņaA de la Peņa,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,w w busseW W Busse,j e gernJ E Gern,c k stoneC K Stone,m nakanoM Nakano,d b muchmoreD B Muchmore,a de la peņaA de la Peņa,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,w w busseW W Busse,

    The suitability of employing AIR Inhaled Insulin (AIR Insulin; AIR is a registered trademark of Alkermes) during acute upper respiratory tract infection (URI) has not been determined. Twenty-one healthy, non-diabetic subjects were enrolled in a single-sequence, two-period, euglycemic clamp study. Subjects received a single 12 U-equivalent dose of AIR Insulin before rhinovirus (RV16) inoculation and during symptomatic infection. Spirometry was used to evaluate pulmonary safety. AIR Insulin exposure (the area under the immunoreactive insulin (IRI) concentration vs time curve from time zero until the IRI concentrations returned to the predose baseline value (AUC(0-t'))) and glucodynamic response (total amount of glucose infused (G(tot))) were comparable before and during RV infection (AUC(0-t') 46,300 vs 52,600 pmol min/l, P=0.21; G(tot) 61,800 vs 68,700 mg, P=0.42, respectively). Variability of pharmacokinetic and pharmacodynamic parameters did not change during URI; either did the number or intensity of adverse events. No significant change in forced expiratory volume or forced vital capacity was observed following AIR Insulin administration or during URI. The AIR Insulin system provides similar pharmacokinetic and glucodynamic responses under conditions of an experimentally induced RV infection and is regarded as suitable for use in diabetic patients during URIs.Clinical Pharmacology & Therapeutics (2008) doi:10.1038/sj.clpt.6100286.

    Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects. Publishing Authors By Initials

    j gernJ Gern,c stoneC Stone,m nakanoM Nakano,d muchmoreD Muchmore,a A ,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,w busseW Busse,je gernJE Gern,ck stoneCK Stone,m nakanoM Nakano,db muchmoreDB Muchmore,a de la peņaA de la Peņa,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,ww busseWW Busse,je gernJE Gern,ck stoneCK Stone,m nakanoM Nakano,db muchmoreDB Muchmore,a de la peņaA de la Peņa,s parkS Park,a suriA Suri,f tibaldiF Tibaldi,d soonD Soon,ww busseWW Busse,

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    Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Molecular therapy : the journal of the American So

    VOLUME: 83

    Page Numbers: 307-11

    Journal Abbreviation: Mol. Ther.

    ISSN: 1525-0016

    DAY: 11

    MONTH: 07

    YEAR: 2007

    Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100890581

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    Grant and Affiliation Information for Effect of Upper Respiratory Tract Infection on AIR Inhaled Insulin Pharmacokinetics and Glucodynamics in Healthy Subjects.

    AFFILIATION: 1Department of Pediatrics, University of Wisconsin Medical School, Madison, Wisconsin, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Mol Ther

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