Search Results - "KOSOGLOU, Teddy"
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JNJ-77242113, a highly potent, selective peptide targeting the IL-23 receptor, provides robust IL-23 pathway inhibition upon oral dosing in rats and humans
Published in Scientific reports (30-07-2024)“…The interleukin (IL)-23 pathway is a pathogenic driver in psoriasis, psoriatic arthritis, and inflammatory bowel disease. Currently, no oral therapeutics…”
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Pharmacodynamics and pharmacokinetics of the novel PAR-1 antagonist vorapaxar (formerly SCH 530348) in healthy subjects
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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Hypothalamic-Pituitary-Adrenal Axis Effects of Mometasone Furoate/Formoterol Fumarate vs Fluticasone Propionate/Salmeterol Administered Through Metered-Dose Inhaler
Published in Chest (01-12-2013)“…Background The effects of mometasone furoate and fluticasone propionate on the hypothalamic-pituitary-adrenal axis were compared when administered from…”
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Disposition of the Selective Cholesterol Absorption Inhibitor Ezetimibe in Healthy Male Subjects
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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HPA Axis Effects of Mometasone Furoate/Formoterol (MF/F) Versus Fluticasone Propionate/Salmeterol (FP/S) Administered via Metered-Dose Inhaler (MDI
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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
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
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
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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Phase 2b Study of Pimodivir (JNJ-63623872) as Monotherapy or in Combination With Oseltamivir for Treatment of Acute Uncomplicated Seasonal Influenza A: TOPAZ Trial
Published in The Journal of infectious diseases (15-03-2019)“…Pimodivir, a first-in-class inhibitor of influenza virus polymerase basic protein 2, is being developed for hospitalized and high-risk patients with influenza…”
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A Phase 2 Study of Pimodivir (JNJ-63623872) in Combination With Oseltamivir in Elderly and Nonelderly Adults Hospitalized With Influenza A Infection: OPAL Study
Published in The Journal of infectious diseases (12-08-2022)“…Abstract Background Both the elderly and individuals with comorbidities are at increased risk of developing influenza-related complications. Novel influenza…”
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Mometasone furoate nasal spray : A review of safety and systemic effects
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
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
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
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
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
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
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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Pharmacokinetics of vorapaxar and its metabolite following oral administration in healthy Chinese and American subjects
Published in International journal of clinical pharmacology and therapeutics (01-10-2014)“…Vorapaxar is a proteaseactivated receptor (PAR)-1 antagonist being developed for the prevention and treatment of thrombotic vascular events. To evaluate…”
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Vorapaxar, an oral PAR-1 receptor antagonist, does not affect the pharmacokinetics and pharmacodynamics of warfarin
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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No differences in the pharmacodynamics and pharmacokinetics of the thrombin receptor antagonist vorapaxar between healthy Japanese and Caucasian subjects
Published in European journal of clinical pharmacology (01-03-2012)“…Background Vorapaxar, a novel antiplatelet agent in advanced clinical development for the prevention and treatment of atherothrombotic disease, is a potent,…”
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