4.5 Article

The effects of age and gender on the pharmacokinetics and pharmacodynamics in healthy subjects of the plasminogen activator, lanoteplase

Journal

BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
Volume 72, Issue 5, Pages 775-786

Publisher

WILEY
DOI: 10.1111/j.1365-2125.2011.04003.x

Keywords

acute myocardial infarction; age and gender effects on pharmacodynamics; age and gender effects on pharmacokinetics; fibrinolytic therapy; plasminogen activation

Funding

  1. Bristol-Myers Squibb Company

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AIMS To investigate the influence of age and gender on the intravenous pharmacokinetics and pharmacodynamics of the plasminogen activator, lanoteplase. METHODS Forty healthy subjects (10 each of young males, elderly males, young females and elderly females) received a single bolus 10 kU kg(-1) intravenous dose of lanoteplase. Plasma from blood serially collected for 24 h post-dose was analyzed for lanoteplase (antigen), fibrinogen, plasminogen and alpha(2)-antiplasmin concentrations, plasma plasminogen activation activity (PPAA) and rapid plasminogen activator inhibitor (PAI-1). RESULTS Lanoteplase mean total systemic clearance (CLt) values ranged from 1.9 to 2.8 I h(-1) and mean steady-state volume of distribution (V-ss) values ranged from 12.3 to 15.6 I. Age-by-gender interactions were observed for lanoteplase CLt (P = 0.04), but no differences were observed for V-ss or elimination half-life. Elderly females had a 27% lower mean CLt than young females (95% CI for the difference 0.17, 1.27 I h(-1)) and 32% lower CLt than elderly males (95% CI for the difference 0.15, 1.65 I h(-1)). PPAA AUC/dose values did not show an age-by-gender interaction. Haemostasis parameters indicated only a slight degree of systemic plasminogen activation. CONCLUSIONS Elderly females had a lower mean lanoteplase CLt than elderly males and young females. However, no difference was observed between young and elderly females for the AUC/dose of PPAA. In addition, there were no age-related or gender-related differences observed in the other pharmacodynamic parameters measured.

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