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Innate Immun ; 18(6): 793-803, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22459966

ABSTRACT

Eritoran, a synthetic analogue of lipid A, has been shown to bind to TLR4/MD-2 complex and thereby block the interaction of endotoxins with TLR4. We report here the results of a study conducted to assess the single-dose safety and tolerability, as well as the pharmacokinetics and pharmacodynamics, of eritoran infusion in Japanese and Caucasian healthy adult men. Sixty-four men (aged 20-45 years; body mass index 18-30 kg/m(2)) were randomized into four groups: 4-mg total dose (six Japanese and six Caucasian men); 12-mg total dose (12 Japanese and 12 Caucasian men); 28-mg total dose (six Japanese and six Caucasian men); and placebo (eight Japanese and eight Caucasian men). Eritoran in single doses up to 28 mg over 4 h was well tolerated, with no apparent ethnic differences noted. Plasma concentrations were slightly higher in Japanese versus Caucasian men; these differences were not significant after adjustment for differences in body mass (clearance: approximately 1.2 ml/h/kg; volume of distribution at steady state: approximately 0.07 l/kg). The ex vivo endotoxin inhibitory activity of eritoran was similar in Japanese and Caucasian men. The data do not indicate any need for clinical dose adjustment for possible ethnic-based differences in drug distribution or metabolism.


Subject(s)
Disaccharides/pharmacokinetics , Sugar Phosphates/pharmacokinetics , Toll-Like Receptor 4/antagonists & inhibitors , Adult , Asian People , Disaccharides/administration & dosage , Disaccharides/adverse effects , Endotoxins/antagonists & inhibitors , Humans , Infusions, Intravenous , Japan , Lipid A/analogs & derivatives , Male , Middle Aged , Protein Binding/drug effects , Sugar Phosphates/administration & dosage , Sugar Phosphates/adverse effects , White People , Young Adult
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