Search Results - "KOSOGLOU, Teddy"

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    Pharmacodynamics and pharmacokinetics of the novel PAR-1 antagonist vorapaxar (formerly SCH 530348) in healthy subjects by Kosoglou, Teddy, Reyderman, Larisa, Tiessen, Renger G., van Vliet, André A., Fales, Robert R., Keller, Robert, Yang, Bo, Cutler, David L.

    Published in European journal of clinical pharmacology (01-03-2012)
    “…Purpose The aim of our study was to evaluate the pharmacology of vorapaxar (SCH 530348), an oral PAR-1 antagonist, in healthy volunteers. Methods and results…”
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    Journal Article
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    Disposition of the Selective Cholesterol Absorption Inhibitor Ezetimibe in Healthy Male Subjects by PATRICK, James E, KOSOGLOU, Teddy, CAYEN, Mitchell N, STAUBER, Kathe L, ALTON, Kevin B, MAXWELL, Stephen E, YALI ZHU, STATKEVICH, Paul, IANNUCCI, Robert, CHOWDHURY, Swapan, AFFRIME, Melton

    Published in Drug metabolism and disposition (01-04-2002)
    “…Ezetimibe [SCH 58235; 1-(4-fluorophenyl)-3( R )-[3-(4-fluorophenyl)-3( S )-hydroxypropyl]-4( S )-(4-hydroxyphenyl)-2-azetidinone], a selective cholesterol…”
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    Once-daily evening dosing of mometasone furoate administered via a dry powder inhaler does not adversely affect the hypothalamic-pituitary-adrenal axis by Kosoglou, Teddy, Cutler, David L, Staudinger, Heribert, Herron, Jerry M

    Published in Chest (01-01-2010)
    “…Inhaled corticosteroids can suppress the hypothalamic-pituitary-adrenal (HPA) axis with long-term exposure. This study reports the effects of moderate-dose…”
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    Mometasone furoate has minimal effects on the hypothalamic-pituitary-adrenal axis when delivered at high doses by Affrime, M B, Kosoglou, T, Thonoor, C M, Flannery, B E, Herron, J M

    Published in Chest (01-12-2000)
    “…To investigate the potential for mometasone furoate (MF) to exert systemic effects following administration by dry powder inhaler (DPI) or metered-dose inhaler…”
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    Effects of Ezetimibe on Cyclosporine Pharmacokinetics in Healthy Subjects by Bergman, Arthur J., Burke, Joanne, Larson, Patrick, Johnson-Levonas, Amy O., Reyderman, Larisa, Statkevich, Paul, Kosoglou, Teddy, Greenberg, Howard E., Kraft, Walter K., Frick, Glenn, Murphy, Gail, Gottesdiener, Keith, Paolini, John F.

    Published in Journal of clinical pharmacology (01-03-2006)
    “…This single‐center, open‐label, 2‐period crossover study investigated the effects of multiple‐dose ezetimibe (EZE) on a single dose of cyclosporine (CyA)…”
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    Mometasone furoate nasal spray : A review of safety and systemic effects by ZITT, Myron, KOSOGLOU, Teddy, HUBBELL, James

    Published in Drug safety (01-01-2007)
    “…The development of corticosteroids that are delivered directly to the nasal mucosa has alleviated much of the concern about the systemic adverse effects…”
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    Neutral endopeptidase inhibition: augmented atrial and brain natriuretic peptide, haemodynamic and natriuretic responses in ovine heart failure by Rademaker, M T, Charles, C J, Espiner, E A, Nicholls, M G, Richards, A M, Kosoglou, T

    Published in Clinical science (1979) (01-09-1996)
    “…1. Atrial and brain natriuretic peptide are both circulating hormones subject to degradation by neutral endopeptidase 24.11. Whereas endogenous levels of…”
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    Ezetimibe : A review of its metabolism, pharmacokinetics and drug interactions by KOSOGLOU, Teddy, STATKEVICH, Paul, JOHNSON-LEVONAS, Amy O, PAOLINI, John F, BERGMAN, Arthur J, ALTON, Kevin B

    Published in Clinical pharmacokinetics (01-01-2005)
    “…Ezetimibe is the first lipid-lowering drug that inhibits intestinal uptake of dietary and biliary cholesterol without affecting the absorption of fat-soluble…”
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    Pharmacokinetics of the novel PAR-1 antagonist vorapaxar in patients with hepatic impairment by Statkevich, Paul, Kosoglou, Teddy, Preston, Richard A., Kumar, Bharath, Xuan, Fengjuan, Trusley, Craig, Schiller, James E., Langdon, Ronald B., Cutler, David L.

    Published in European journal of clinical pharmacology (01-11-2012)
    “…Purpose To determine whether hepatic impairment has an effect on the pharmacokinetics (PK) of vorapaxar or M20, its main pharmacologically active metabolite…”
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    The Effect of Multiple Doses of Ketoconazole or Rifampin on the Single- and Multiple-Dose Pharmacokinetics of Vorapaxar by Kosoglou, Teddy, Statkevich, Paul, Kumar, Bharath, Xuan, Fengjuan, Schiller, James E., Johnson-Levonas, Amy O., Young, Sophia, Cutler, David L.

    Published in Journal of clinical pharmacology (01-05-2013)
    “…This randomized, open‐label, parallel‐group study evaluated the effects of multiple‐dose ketoconazole or rifampin on the single‐ and multiple‐dose…”
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    Pharmacokinetics and pharmacodynamics of the novel PAR-1 antagonist vorapaxar in patients with end-stage renal disease by Kosoglou, Teddy, Kraft, Walter K., Kumar, Bharath, Statkevich, Paul, Xuan, Fengjuan, Ma, Lei, Jennings, Lisa K., Schiller, James E., Langdon, Ronald B., Cutler, David L.

    Published in European journal of clinical pharmacology (01-07-2012)
    “…Purpose To determine whether impaired renal function alters the pharmacokinetics (PK) of vorapaxar or its ability to inhibit thrombin receptor agonist peptide…”
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    No Pharmacokinetic Drug–Drug Interaction Between Prasugrel and Vorapaxar Following Multiple‐Dose Administration in Healthy Volunteers by Anderson, Matt S., Kosoglou, Teddy, Statkevich, Paul, Li, Jing, Rotonda, Jennifer, Meehan, Alan G., Cutler, David L.

    Published in Clinical pharmacology in drug development (01-02-2018)
    “…Vorapaxar is a first‐in‐class antagonist of the protease‐activated receptor‐1, the primary thrombin receptor on human platelets, which mediates the downstream…”
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    Vorapaxar, an oral PAR-1 receptor antagonist, does not affect the pharmacokinetics and pharmacodynamics of warfarin by Kosoglou, Teddy, Zhu, Yali, Xuan, Fengjuan, Black, Laura, Johnson-Levonas, Amy O., Martinho, Monika, Statkevich, Paul, Cutler, David L.

    Published in European journal of clinical pharmacology (01-11-2012)
    “…Purpose Vorapaxar is an orally active protease-activated receptor 1 (PAR-1) antagonist that inhibits thrombin-induced platelet aggregation. This open-label…”
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